32 Bristol Myers Squibb jobs in Hamilton Township
Quality Control Technician
08876 Somerville, New Jersey
Lilly
Posted today
Job Viewed
Job Description
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Lilly employees embrace Operational Excellence in everything we do, to achieve our mission of Making
Medicine with Safety First & Quality Always; following our common purpose under TEAM Lilly and our
Manufacturing Standards under the strict code of conduct guided by our Red Book assuring data integrity in all we do in order to deliver a reliable supply of medicine for people around the world.
**Position Brand Description:**
This position conducts routine lab support activities including sampling of controlled utilities (water and gas
systems), collection, aliquoting, weighing, shipping and disposal of raw materials, in-process and drug
substance samples as assigned by Supervisor. Performs routine QC responsibilities as needed. Applies cGMP
practices during the execution of all work tasks. Exhibits strong teamwork skills. Updates supervisor of
progress on a regular basis.
**Key Objectives/Deliverables:**
**Manage for Results /Strategic Planning:**
1. Conducts routine sampling of utilities such as water systems and gases as assigned by supervisor and
delivers to the relevant QC laboratory for analysis.
2. Collects microbiology and analytical samples from manufacturing and delivers to the QC laboratories.
Works weekends, holidays, and overtime as needed.
3. Performs routine aliquoting of QC samples as directed by supervisor.
4. Performs routine QC responsibilities such as lab equipment maintenance, QC inventory control
reconciliation and disposal of samples.
**Manage Relationships with Key Stakeholders and Customers:**
N/A
**Staff Development and Management:**
N/A
**Resource Management:**
N/A
**Basic Requirements:**
1. 0 - 2 years of previous related experience
2. Attentive to detail.
3. Good teamwork and communication skills.
4. Exposure to cGMP regulations and work experience in a regulated environment are preferred.
5. Adequate computer skill.
6. Employees must be flexible working various shifts (4 day work week, 5 day work week, including
weekends, early and late shifts) and "call in" time to support business needs will be required.
**Additional Preferences:**
1. Associate degree
**Education Requirements:**
1. High School Diploma
**Other Information:**
1. Travel not required.
2. Lifting required NMT 50 lbs.
3. May be required to be on call.
4. Employees must be flexible working various shifts (4-day work week, 5-day work week, including
weekends, early and late shifts) and "call in" time to support manufacturing and/or meet business needs
may be required.
5. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color,
religion, gender, sexual orientation, gender identity, gender expression, national origin, protected
veteran status, disability or any other legally protected status.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$19.83 - $38.08
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Lilly employees embrace Operational Excellence in everything we do, to achieve our mission of Making
Medicine with Safety First & Quality Always; following our common purpose under TEAM Lilly and our
Manufacturing Standards under the strict code of conduct guided by our Red Book assuring data integrity in all we do in order to deliver a reliable supply of medicine for people around the world.
**Position Brand Description:**
This position conducts routine lab support activities including sampling of controlled utilities (water and gas
systems), collection, aliquoting, weighing, shipping and disposal of raw materials, in-process and drug
substance samples as assigned by Supervisor. Performs routine QC responsibilities as needed. Applies cGMP
practices during the execution of all work tasks. Exhibits strong teamwork skills. Updates supervisor of
progress on a regular basis.
**Key Objectives/Deliverables:**
**Manage for Results /Strategic Planning:**
1. Conducts routine sampling of utilities such as water systems and gases as assigned by supervisor and
delivers to the relevant QC laboratory for analysis.
2. Collects microbiology and analytical samples from manufacturing and delivers to the QC laboratories.
Works weekends, holidays, and overtime as needed.
3. Performs routine aliquoting of QC samples as directed by supervisor.
4. Performs routine QC responsibilities such as lab equipment maintenance, QC inventory control
reconciliation and disposal of samples.
**Manage Relationships with Key Stakeholders and Customers:**
N/A
**Staff Development and Management:**
N/A
**Resource Management:**
N/A
**Basic Requirements:**
1. 0 - 2 years of previous related experience
2. Attentive to detail.
3. Good teamwork and communication skills.
4. Exposure to cGMP regulations and work experience in a regulated environment are preferred.
5. Adequate computer skill.
6. Employees must be flexible working various shifts (4 day work week, 5 day work week, including
weekends, early and late shifts) and "call in" time to support business needs will be required.
**Additional Preferences:**
1. Associate degree
**Education Requirements:**
1. High School Diploma
**Other Information:**
1. Travel not required.
2. Lifting required NMT 50 lbs.
3. May be required to be on call.
4. Employees must be flexible working various shifts (4-day work week, 5-day work week, including
weekends, early and late shifts) and "call in" time to support manufacturing and/or meet business needs
may be required.
5. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color,
religion, gender, sexual orientation, gender identity, gender expression, national origin, protected
veteran status, disability or any other legally protected status.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$19.83 - $38.08
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
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0
Quality Control Specialist
08544 Princeton, New Jersey
Actalent
Posted 1 day ago
Job Viewed
Job Description
Job Title: Quality Control Specialist
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Princeton,NJ.
Application Deadline
This position is anticipated to close on Oct 21, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Princeton,NJ.
Application Deadline
This position is anticipated to close on Oct 21, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
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1
Quality Control I
08854 Piscataway, New Jersey
Adecco US, Inc.
Posted 2 days ago
Job Viewed
Job Description
Adecco is assisting a local client recruiting for Quality Control Technician opportunities in Piscataway, NJ.
This is an excellent opportunity to join a winning culture and get your foot in the door with the world's largest cosmetics company, known for its innovation and leadership in beauty and personal care. If Quality Control Technician sounds like something you would be interested in, and you meet the qualifications listed below, apply now!
**Responsibilities for a Quality Control Technician include but are not limited to:**
+ Perform routine inspections and tests on finished goods and components using physical, chemical, or functional testing methods.
+ Maintain accurate records of inspections, test results, and laboratory activities in compliance with SOPs and GMPs.
+ Assist with equipment maintenance and calibration to ensure proper functionality and compliance.
+ Manage samples by collecting, labeling, storing, and disposing of them according to protocols.
**Candidates for Quality Control Technician must meet the following requirements to be considered:**
+ Experience in quality control or laboratory testing in a manufacturing or production environment.
+ Strong attention to detail and ability to follow SOPs, GMPs, and safety regulations.
+ Effective communication and collaboration skills across departments.
+ Must be able to lift/sort boxes and assist with general lab support tasks as needed.
**What's in this Quality Control Technician position for you?**
+ Pay: $ 26.51/hour
+ Shift: Monday - Friday, 6:45am - 2:45pm
+ Weekly paycheck
+ Dedicated Onboarding Specialist & Recruiter
+ Access to Adecco's Aspire Academy with thousands of free upskilling courses
**This Quality Control Technician role is being recruited for by one of our Centralized Delivery Team and not your local Branch.** For instant consideration for this position and other opportunities with Adecco in Piscataway, NJ, apply today!
**Pay Details:** $26.51 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
**Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
This is an excellent opportunity to join a winning culture and get your foot in the door with the world's largest cosmetics company, known for its innovation and leadership in beauty and personal care. If Quality Control Technician sounds like something you would be interested in, and you meet the qualifications listed below, apply now!
**Responsibilities for a Quality Control Technician include but are not limited to:**
+ Perform routine inspections and tests on finished goods and components using physical, chemical, or functional testing methods.
+ Maintain accurate records of inspections, test results, and laboratory activities in compliance with SOPs and GMPs.
+ Assist with equipment maintenance and calibration to ensure proper functionality and compliance.
+ Manage samples by collecting, labeling, storing, and disposing of them according to protocols.
**Candidates for Quality Control Technician must meet the following requirements to be considered:**
+ Experience in quality control or laboratory testing in a manufacturing or production environment.
+ Strong attention to detail and ability to follow SOPs, GMPs, and safety regulations.
+ Effective communication and collaboration skills across departments.
+ Must be able to lift/sort boxes and assist with general lab support tasks as needed.
**What's in this Quality Control Technician position for you?**
+ Pay: $ 26.51/hour
+ Shift: Monday - Friday, 6:45am - 2:45pm
+ Weekly paycheck
+ Dedicated Onboarding Specialist & Recruiter
+ Access to Adecco's Aspire Academy with thousands of free upskilling courses
**This Quality Control Technician role is being recruited for by one of our Centralized Delivery Team and not your local Branch.** For instant consideration for this position and other opportunities with Adecco in Piscataway, NJ, apply today!
**Pay Details:** $26.51 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
**Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
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2
Quality Control Technician
08816 East Brunswick, New Jersey
Aerotek
Posted 7 days ago
Job Viewed
Job Description
**Job Title: Quality Control Technician**
**Job Description**
We are seeking a dedicated Quality Control Technician for the 3rd shift to join our growing team. This role is integral in ensuring the production of high-quality food products in a safe and clean environment.
**Responsibilities**
+ Ensure new workers are trained accordingly.
+ Maintain housekeeping standards to ensure a clean and safe workplace.
+ Work closely with other Production Supervisors to ensure effective production handovers.
**Essential Skills**
+ Bi-lingual Spanish required for effective communication with production staff.
+ Positive attitude and pleasant personality for efficient communication with diverse populations.
+ Self-motivation and a results-oriented approach.
+ Understanding of principles, practices, and procedures of the food manufacturing environment.
+ Ability to lead and motivate others to achieve productivity goals.
**Additional Skills & Qualifications**
+ Experience in quality control, GMP, food manufacturing/packaging quality, inspection, packaging, and production.
**Why Work Here?**
Join a dynamic and growing company that has doubled in size over the last five years, offering a stable work environment with a structured and predictable workflow.
**Work Environment**
This position is located in the Cookies Production - Mixing/Mini Pan department, within a standard food production warehouse environment. You will work near moving equipment such as forklifts and machinery like conveyor belts and production machinery, with exposure to moderate to loud noise and fluorescent lighting. Cleanliness and sanitation are required. Shifts typically last 8-12 hours, and you may work during the day or night, surrounded by the smells of cookies and other food products. The facility manufactures products that may contain peanuts and tree nuts.
**Job Type & Location**
This is a Contract to Hire position based out of East Brunswick, New Jersey.
**Pay and Benefits**
The pay range for this position is $20.25 - $20.25/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)
**Workplace Type**
This is a fully onsite position in East Brunswick,NJ.
**Application Deadline**
This position is anticipated to close on Oct 10, 2025.
**About Aerotek:**
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
**Job Description**
We are seeking a dedicated Quality Control Technician for the 3rd shift to join our growing team. This role is integral in ensuring the production of high-quality food products in a safe and clean environment.
**Responsibilities**
+ Ensure new workers are trained accordingly.
+ Maintain housekeeping standards to ensure a clean and safe workplace.
+ Work closely with other Production Supervisors to ensure effective production handovers.
**Essential Skills**
+ Bi-lingual Spanish required for effective communication with production staff.
+ Positive attitude and pleasant personality for efficient communication with diverse populations.
+ Self-motivation and a results-oriented approach.
+ Understanding of principles, practices, and procedures of the food manufacturing environment.
+ Ability to lead and motivate others to achieve productivity goals.
**Additional Skills & Qualifications**
+ Experience in quality control, GMP, food manufacturing/packaging quality, inspection, packaging, and production.
**Why Work Here?**
Join a dynamic and growing company that has doubled in size over the last five years, offering a stable work environment with a structured and predictable workflow.
**Work Environment**
This position is located in the Cookies Production - Mixing/Mini Pan department, within a standard food production warehouse environment. You will work near moving equipment such as forklifts and machinery like conveyor belts and production machinery, with exposure to moderate to loud noise and fluorescent lighting. Cleanliness and sanitation are required. Shifts typically last 8-12 hours, and you may work during the day or night, surrounded by the smells of cookies and other food products. The facility manufactures products that may contain peanuts and tree nuts.
**Job Type & Location**
This is a Contract to Hire position based out of East Brunswick, New Jersey.
**Pay and Benefits**
The pay range for this position is $20.25 - $20.25/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)
**Workplace Type**
This is a fully onsite position in East Brunswick,NJ.
**Application Deadline**
This position is anticipated to close on Oct 10, 2025.
**About Aerotek:**
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
View Now
3
Quality Control Specialist
08544 Princeton, New Jersey
Actalent
Posted 8 days ago
Job Viewed
Job Description
Job Title: Quality Control Specialist
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Princeton,NJ.
Application Deadline
This position is anticipated to close on Oct 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Princeton,NJ.
Application Deadline
This position is anticipated to close on Oct 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
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4
Quality Control Specialist
08544 Princeton, New Jersey
Actalent
Posted 13 days ago
Job Viewed
Job Description
Job Title: Quality Control Specialist
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Princeton,NJ.
Application Deadline
This position is anticipated to close on Oct 9, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Princeton,NJ.
Application Deadline
This position is anticipated to close on Oct 9, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now
5
Quality Control Sampler
08544 Princeton, New Jersey
Sun Pharmaceuticals, Inc
Posted 15 days ago
Job Viewed
Job Description
**Job Summary**
The QC Sampler is responsible for sampling all incoming materials such as raw materials, packaging components, printed material and all other GMP materials using established Standard Operating Procedures (SOPs) and working in accordance with current Good Manufacturing Practices (cGMP). Collect, sample, and prepare QC Chemical test samples for various analysis laboratories when required.
**Area Of Responsibility**
+ Sample all incoming materials and packaging materials per procedures.
+ Inspect all incoming GMP materials per materials specifications Inspect all incoming GMP materials per materials specifications including Identify non-conforming materials cleanliness and defects.
+ Follow work-flow procedures from receiving test samples, monitoring inventories, to waste disposal
+ Train towards Visual Inspection qualifications
+ Accurately sample and weigh Chemical test samples according to Material Specifications and SOPs using, at times, sterile operating procedures
+ Perform QC Release testing for Visual Inspection of cosmetic defects and dimensional inspection of product container closure components
+ Initiate product non-conforming reports (UPD) as required (Track Wise) and investigate any problems noted with sampling/inspection process.
+ Issue/Dispense and receive labels and packaging materials per production batch record. Keep inventory of all product label/packaging materials
+ Enter transactions/transfers into SAP inventory control system
+ Maintain records/manual log books per good documentation practices (GDPs)
+ Coordinate scrap removal of rejected product
+ Update Raw Material Specifications (RMS)/(SOPs) as needed
+ Work under general supervision and follows established procedures and instructions
+ Operate and maintain the QC Chemical Sampling laboratory to GMP compliance and safety compliance
+ Operate, maintain and clean, and calibrate balances
+ Maintain laboratory supplies, reagents, chemicals, and equipment inventories for Sampling and Inspection laboratories
+ Manage calibration of instruments and equipment used for inspection and perform monthly equipment/ instrument maintenance and cleaning.
+ Other duties as assigned
**Work Conditions:**
Warehouse Environment
Laboratory environment:
+ Exposure to noise, bio-hazardous (live cultures), and chemicals
+ Exposure to non-hazardous and hazardous chemicals and materials
+ Moderate noise, oven heat, open flame, chemical fume hoods areas requiring wearing appropriate safety equipment (i.e. gloves, lab coat, safety glasses and respirator)
**Physical Requirements:**
+ Stand, sit, walk, use hands and fingers to handle or feel, reach with arms and hands, talk or hear, stoop, kneel, crouch or crawl.
+ Able to operate basic mechanical tools (i.e.:) calipers, micrometers, and go no-go gages
+ Able to drive a fork truck/tow motor/operate forklift
+ Close vision; depth perception; ability to adjust focus
+ Use of repetitive motion
+ Able to operate computer/office machines
+ Able to lift and carry up to 50 lbs.
**Travel Estimate**
Up to 5 %
**Education and Job Qualification**
+ Minimum of High School/Trade School/Vocational School Diploma, GED, or equivalent. B.S. degree preferred.
+ The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).
+ Good oral and written communication skills and ability to use these skills to follow specific instruction and report assay results (i.e. written SOPs)
+ Proficient with wet chemical methods and tests (USP, ACS, Titration, Limit tests, etc.)
+ Fundamental knowledge of chemical principles
+ Proficient with basic laboratory instrumentation.
+ Use of Track Wise software and knowledge of SAP is preferred.
+ Use of Lotus Notes software
+ Working knowledge of Microsoft Office Applications.
+ A self-starter with a hands-on approach and a can-do attitude.
**Experience**
+ Minimum of two (2) years of experience required in a Pharmaceutical/drug (FDA Regulated) industry preferred
**_Disclaimer:_** _The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)._
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
The QC Sampler is responsible for sampling all incoming materials such as raw materials, packaging components, printed material and all other GMP materials using established Standard Operating Procedures (SOPs) and working in accordance with current Good Manufacturing Practices (cGMP). Collect, sample, and prepare QC Chemical test samples for various analysis laboratories when required.
**Area Of Responsibility**
+ Sample all incoming materials and packaging materials per procedures.
+ Inspect all incoming GMP materials per materials specifications Inspect all incoming GMP materials per materials specifications including Identify non-conforming materials cleanliness and defects.
+ Follow work-flow procedures from receiving test samples, monitoring inventories, to waste disposal
+ Train towards Visual Inspection qualifications
+ Accurately sample and weigh Chemical test samples according to Material Specifications and SOPs using, at times, sterile operating procedures
+ Perform QC Release testing for Visual Inspection of cosmetic defects and dimensional inspection of product container closure components
+ Initiate product non-conforming reports (UPD) as required (Track Wise) and investigate any problems noted with sampling/inspection process.
+ Issue/Dispense and receive labels and packaging materials per production batch record. Keep inventory of all product label/packaging materials
+ Enter transactions/transfers into SAP inventory control system
+ Maintain records/manual log books per good documentation practices (GDPs)
+ Coordinate scrap removal of rejected product
+ Update Raw Material Specifications (RMS)/(SOPs) as needed
+ Work under general supervision and follows established procedures and instructions
+ Operate and maintain the QC Chemical Sampling laboratory to GMP compliance and safety compliance
+ Operate, maintain and clean, and calibrate balances
+ Maintain laboratory supplies, reagents, chemicals, and equipment inventories for Sampling and Inspection laboratories
+ Manage calibration of instruments and equipment used for inspection and perform monthly equipment/ instrument maintenance and cleaning.
+ Other duties as assigned
**Work Conditions:**
Warehouse Environment
Laboratory environment:
+ Exposure to noise, bio-hazardous (live cultures), and chemicals
+ Exposure to non-hazardous and hazardous chemicals and materials
+ Moderate noise, oven heat, open flame, chemical fume hoods areas requiring wearing appropriate safety equipment (i.e. gloves, lab coat, safety glasses and respirator)
**Physical Requirements:**
+ Stand, sit, walk, use hands and fingers to handle or feel, reach with arms and hands, talk or hear, stoop, kneel, crouch or crawl.
+ Able to operate basic mechanical tools (i.e.:) calipers, micrometers, and go no-go gages
+ Able to drive a fork truck/tow motor/operate forklift
+ Close vision; depth perception; ability to adjust focus
+ Use of repetitive motion
+ Able to operate computer/office machines
+ Able to lift and carry up to 50 lbs.
**Travel Estimate**
Up to 5 %
**Education and Job Qualification**
+ Minimum of High School/Trade School/Vocational School Diploma, GED, or equivalent. B.S. degree preferred.
+ The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).
+ Good oral and written communication skills and ability to use these skills to follow specific instruction and report assay results (i.e. written SOPs)
+ Proficient with wet chemical methods and tests (USP, ACS, Titration, Limit tests, etc.)
+ Fundamental knowledge of chemical principles
+ Proficient with basic laboratory instrumentation.
+ Use of Track Wise software and knowledge of SAP is preferred.
+ Use of Lotus Notes software
+ Working knowledge of Microsoft Office Applications.
+ A self-starter with a hands-on approach and a can-do attitude.
**Experience**
+ Minimum of two (2) years of experience required in a Pharmaceutical/drug (FDA Regulated) industry preferred
**_Disclaimer:_** _The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)._
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
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6
Chemist, Quality Control
08544 Princeton, New Jersey
Sun Pharmaceuticals, Inc
Posted 15 days ago
Job Viewed
Job Description
Chattem Chemicals, Inc. (a Sun Pharma Company) has a rich history as part of Chattem, Inc, which was founded as the Chattanooga Medicine Company on February 21, 1879. Today Chattem Chemicals, Inc. manufacturers a broad variety of products in four primary markets: Active Pharmaceutical Ingredients, Catalysts, Surfactants & Performance Additives.
Responsibilities:
1. Analytical support to all departments.
1. Support to regular QC activities, as required.
1. Method development, including validation and documentation.
1. Writing concise and timely reports to management on projects and regular activities.
1. Responsible for customer complaint investigations.
1. Assisting with technician training.
1. Other duties, as assigned.
Qualifications:
1. Bachelor of Chemistry degree (or related degree)
2. Knowledge of basic chemistry principles and analytical methods.
3. Working knowledge of cGMP as they relate to lab activities.
4. Careful attention to detail.
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Responsibilities:
1. Analytical support to all departments.
1. Support to regular QC activities, as required.
1. Method development, including validation and documentation.
1. Writing concise and timely reports to management on projects and regular activities.
1. Responsible for customer complaint investigations.
1. Assisting with technician training.
1. Other duties, as assigned.
Qualifications:
1. Bachelor of Chemistry degree (or related degree)
2. Knowledge of basic chemistry principles and analytical methods.
3. Working knowledge of cGMP as they relate to lab activities.
4. Careful attention to detail.
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
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7
Quality Control Specialist
Hamilton Township, New Jersey
Bright Future USA
Posted today
Job Viewed
Job Description
Job Description
Job Description
Job Summary:
As a Quality Control Specialist, you will play a critical role in ensuring that our products meet established standards of quality, reliability, and performance. You will be responsible for conducting inspections, identifying quality issues, and working with cross-functional teams to implement corrective actions.
Key Responsibilities:
Perform routine product and process inspections according to company and industry standards.
Identify, document, and report defects or inconsistencies in products or processes.
Collaborate with production, engineering, and supply chain teams to resolve quality issues.
Maintain accurate records of inspection results and generate quality reports.
Participate in internal audits and support external audit processes.
Assist in developing and implementing quality control policies and procedures.
Recommend improvements to enhance product quality and customer satisfaction.
Qualifications:
High school diploma or equivalent required
2+ years of experience in a quality control or quality assurance role (industry-specific experience is a plus).
Strong attention to detail and excellent analytical skills.
Familiarity with inspection tools and techniques (e.g., calipers, micrometers, visual inspection).
Knowledge of ISO standards and quality management systems (e.g., ISO 9001) is a plus.
Proficient in Microsoft Office Suite and/or quality control software.
Strong communication and problem-solving skills.
What We Offer:
Competitive salary and benefits package
Medical, 401k after 90 days, Paid Time Off
Opportunities for professional development and growth
A collaborative and supportive team environment
Bright Future USA is a subsidiary of Ikio LED Lighting Company is a leading manufacturer and supplier of energy-efficient lighting solutions, specializing in LED (Light Emitting Diode) technology. Founded on the principles of innovation, sustainability, and customer satisfaction, Ikio is committed to providing high-quality lighting products that meet the diverse needs of residential, commercial, and industrial clients.
Company DescriptionBright Future USA is a subsidiary of Ikio LED Lighting Company is a leading manufacturer and supplier of energy-efficient lighting solutions, specializing in LED (Light Emitting Diode) technology. Founded on the principles of innovation, sustainability, and customer satisfaction, Ikio is committed to providing high-quality lighting products that meet the diverse needs of residential, commercial, and industrial clients.
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8
Supv Quality Control
08869 Raritan, New Jersey
Johnson and Johnson
Posted 18 days ago
Job Viewed
Job Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at
Job Function:
QualityJob Sub Function:
Quality ControlJob Category:
People LeaderAll Job Posting Locations:
Raritan, New Jersey, United States of AmericaJob Description:
Janssen Pharmaceutical, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Supervisor, QC Release (S-W Day Shift) in Raritan, NJ!
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at and follow us @JanssenGlobal. Janssen Biotech, Inc. is part of the Janssen Pharmaceutical Companies.
Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR-T platform and investigational treatment.
Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our cell therapy products? Apply today for this exciting opportunity to be part of the #CAR-T team!
The QC Supervisor is responsible for overseeing day-to-day Quality Control activities for a designated functional laboratory, ensuring GMP compliance, accuracy, and timeliness of specified testing processes. They carry out duties in compliance with all local, state, and federal regulations and guidelines (including FDA, EPA, and OSHA) as well as all company and site policies and procedures. They will also support internal and external audits. They will typically guide daily work activities of 10-12 direct staff within a functional laboratory of the Quality Control department. They are responsible for interviewing, hiring, performance review, rewarding and disciplining employees, addressing complaints, and resolving conflict.
Key Responsibilities:- Manage analyst schedule to support Drug Product testing
- Review/approve QC laboratory data for validity and accuracy according to cGMP/cGLP standards
- Review/approve documents as a QC department subject matter expert (SME)
- Oversee timely completion of laboratory investigation of OOS/ invalid assays, CAPAs and change controls
- Ensure accuracy and completeness of executed analytical method transfer activities
- Set testing priorities and manage work assignments
- Mentor, train, and supervise quality control staff, as well as evaluate performance and provide opportunities for growth
- Communicate department objectives and metrics
- Support internal and Health Authority audits, as well as audit related investigations
- Minimum of a Bachelor’s or equivalent University degree required; advanced degree (MSc., Ph.D.) or focused degree in Biology, Biochemistry, or related scientific field is preferred
Required:
- Minimum 6 years of relevant work experience
- Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, Flow Cytometry, ELISA, Cell Culture, and/or Potency assays
- Knowledge of cGMP regulations and Good Documentation Practices (GDP)
- Detailed knowledge of Compendial (e.g., USP, EP, JP, etc.) requirements and standards for QC testing
- Proficient knowledge of analytical technologies used in a Quality Control laboratory and method transfer
- Experience leading, coaching, or supervising direct or indirect personnel or teams
- Work experience in Cell and/or Gene Therapy or Biologics
- Experience with LIMs and SAP or equivalent systems
- Requires ability and flexibility to work 10-hour shifts between the operational hours of 7AM-5PM (Sunday - Wednesday), and provide occasional support on the weekends or other shifts
- Requires the ability to meet the physical demands (lift up to 20 lbs, stand or sit for extended periods of time in a laboratory setting)
- Requires up to 5% domestic travel to other sites/locations
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.
The anticipated base pay range for this position is :
$91,000-$147,200Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave – 10 days Volunteer Leave – 4 days Military Spouse Time-Off – 80 hours Additional information can be found through the link below.
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9