6,965 Quality Control Specialist jobs in the United States

Yoh is hiring for a Quality Control Specialist for our pharmaceutical client in Noblesville, Indiana.  The Quality Control Specialist role is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with regulatory and company standards. This role is critical to maintaining product quality, supporting production timelines, and ensuring regulatory compliance.

Location:  Noblesville, IN
Hours:  Monday - Friday, 8AM - 5PM 

Essential Functions:

• Perform routine and non-routine analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, titration, ICP-MS etc.
• Conduct testing on raw materials, intermediates, and finished products in accordance with cGMP and SOPs.
• Review and interpret analytical data; prepare detailed and accurate reports and documentation.
• Maintain laboratory equipment, including calibration, qualification, and troubleshooting.
• Participate in method development, method validation, and stability studies as required.
• Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, ICH) and internal quality standards.
• Support investigations (OOS, OOT, deviations) and assist in root cause analysis and CAPA implementation.
• Maintain a clean and organized laboratory environment and adhere to safety guidelines.
• Participate in audits and inspections and support documentation requests from regulatory authorities.
  

Requirements    

• Bachelor of Science in Biology, Chemistry or related field required.
• 2 or more years of relevant experience required.
• Solid knowledge of analytical techniques and instrumentation (HPLC, GC, etc.).
• Familiarity with cGMP, GLP, and regulatory guidelines.
• Must be able to resolve problems, handle conflict and make effective decisions under pressure, and conduct Root Cause Analysis
• Ability to do simple to complex math calculations, input data into the computer and analyze data as required.
• Ability to multitask projects.
• Must be proficient in use of Microsoft suite office products.
• Good computer skills, including utilizing personal computers and data entry programs Good hands on, analytical, and problem solving and decision making skills.
• Excellent writing and verbal communications skills.
• Ability to work independently and with others to accomplish goals and priorities High level of energy and regular, consistent attendance.
• Verifiable working knowledge of cGMP guidelines and their application in a pharmaceutical manufacturing environment.
  

#IND-SPG

Estimated Min Rate : $26.00
Estimated Max Rate : $28.00


What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:

• Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
• Health Savings Account (HSA) (for employees working 20+ hours per week)
• Life & Disability Insurance (for employees working 20+ hours per week)
• MetLife Voluntary Benefits
• Employee Assistance Program (EAP)
• 401K Retirement Savings Plan
• Direct Deposit & weekly epayroll
• Referral Bonus Programs
• Certification and training opportunities
  

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

Yoh is hiring a Quality Control Specialist  for our Los Angeles, CA client. In the Quality Control Specialist,  you will be focused and responsible for the qualification of all the Raw Materials, Fragrances and Bulk/Intermediate.

Industry : Personal Care/ Cosmetics
Location : El Segundo, CA
 
Job Functions

• Help Develop, implement and maintain QC systems and measures.
• Inspect and test Raw Materials, Fragrances, In-Process and Customer supplied bulk, against specification to ensure quality standards are met.
• Issue adjustments to In-Process Bulk if necessary.
• Complete Inspections forms for Finished Bulk/Intermediate and /or Raw Materials and Fragrances.
• Update status of Raw Materials and /or Bulk/Intermediate in ERP system.
• Communicate quality control information to all relevant organizational departments.
• Produce and communicate reports regarding nonconformance of products.
• Assist in investigations related to Nonconformance or OOS, Customer Complaint etc.
• Maintain the raw material retains for the Department.
• Assist in updating or writing Department related SOPs and Work Instructions or other Department related documents.
• Assist in Raw Materials and Bulk /Intermediate Cycle Counts and Full Inventories
• Consistently demonstrates excellent interpersonal skills and professionalism to company management, all levels of staff and vendors and outside agencies.
• Complete all other additional tasks assigned by supervisor.
• Adhere to company policies and procedures and sets a positive example for others within the organization.

Education, Licensure and/or Experience

• Bachelor’s degree in science (chemistry, pharmacy, or biology) or equivalent work experience. 
• 2+ years Quality Control related experience in a cGMP OTC manufacturing environment.
• Proficient use of Microsoft Office products including Word, Excel, Outlook and PowerPoint. 
• Ability to quickly learn new software programs as needed.
• Experience using common laboratory equipment such as pH Meter; Refractive Index; Pycnometer; Brookfield Viscometer; Color Matching; Scales; and lab mixers

#IND-SPG

Estimated Min Rate : $23.00
Estimated Max Rate : $24.00


What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:

• Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
• Health Savings Account (HSA) (for employees working 20+ hours per week)
• Life & Disability Insurance (for employees working 20+ hours per week)
• MetLife Voluntary Benefits
• Employee Assistance Program (EAP)
• 401K Retirement Savings Plan
• Direct Deposit & weekly epayroll
• Referral Bonus Programs
• Certification and training opportunities
  

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

**Quality Control Specialist**
Kelly® Science & Clinical is seeking a Quality Control Specialist for **a 6-month contract** position at **a premier biotech** company in **Redwood City, CA** . If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
**Pay Rate:**
$65-75/hour
**Overview** :
In this role, you will support the implementation and configuration of Veeva LIMS in the QC laboratory, create and revise SOPs, and assist with day-to-day lab operations and data integrity.
**Schedule:**
Monday-Friday, standard working hours
**Responsibilities:**
+ Support the implementation and configuration of Veeva LIMS and Blue Mountain systems in the QC laboratory.
+ Create and revise standard operating procedures (SOPs) related to stability, validation, and test methods.
+ Perform routine lab activities, including data review, laboratory maintenance, sample receipt and disposal, and chart recorder upkeep.
+ Assist with laboratory investigations, OOT/OOS deviations, change controls, and CAPAs.
+ Collaborate closely with the QC team to ensure smooth system integration and effective documentation.
+ Other duties as assigned.
**Qualifications:**
+ BS in Analytical Chemistry, Biochemistry or Biological Sciences or equivalent
+ 8+ years of industrial Quality Control experience
+ Strong knowledge in QC lab related processes, GDP, and data integrity
+ Strong working knowledge and hands-on experience with Veeva LIMS
**What happens next:**
Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

With Staff Management | SMX, you'll get a weekly paycheck, learn new skills, meet new people, and work with a great management team in a clean and safe environment.
Looking for your next opportunity? Join Staff Management | SMX as a Quality Control Specialist in Gardena, CA! We're seeking detailed-oriented individuals to support our client's Airport Cargo operations.
.
Perks & Benefits: Paid Training, Weekly paychecks, Direct Deposit or Cash Card pay options, Medical / Dental Insurance, Paid Sick Leave, Paid Time Off, Referral Bonus (Restrictions Apply).
Bonus: Bonus is per eligibility requirements.
Shifts: Rotating Shifts, All Shifts.
Employment Types: Full Time, Seasonal, Temporary or Contract, Long Term.
Pay Rate: $19.50 - $2.00 / hour
Duties:
+ Verify assembly compliance to airline/company specifications.
+ Flight is assembled in the correct equipment type.
+ Crew meal count and special dietary specification are correct.
+ All components, entrees, or supply/beverage item are complete.
+ Initiate the correction of missing or wrong items packed with assembly team members and capture the actions taken in QC tracking system (Smartsheet).
+ Partner with assembly leadership to initiate proactive coaching sessions to mitigate repeat defects.
+ Weekly check-ins with CI and Department Manager(s) to discuss defect trends and additional actions needed by department leadership to correct.
+ Other duties as assigned by CI Manager.
.
Position Requirements:
**QUALIFICATIONS:**
+ Basic math skills (add, subtract, multiply, divide).
+ Problem-solving skills: ability to make independent decisions.
+ Effective written and verbal communications.
+ Ability to use computer and mobile /tablet electronic devices.
+ Must have the ability to work under pressure while maintaining composure.
+ Ability to provide constructive feedback and coaching.
+ Fast-paced assembly experience preferred.
+ Quality control experience preferred.
+ Experience working in cold environment preferred.
Requirements: Background Check, Drug Test, Stand for Shift Duration, Must be at least 18 years old., required education: HS Diploma or GED.
Work Location: SMX @ Air Fayre, 1720 W 135th St, Gardena, CA 90249.
Job Types: Distribution, Food Production, General Production, General Warehouse, Hand Packaging, Manufacturing, Administrative/Clerical.
Industry: Warehouse/Distribution.
The hourly rate for this position is anticipated between 19.50 - 22.00 per hour. This range is a good-faith estimate, based on the shift you work and other considerations permitted by law. An employee''s pay history will not be a contributing factor where prohibited by local law. In addition to monetary compensation, we offer medical, dental, vision, life, and more. More details about benefits can be found at .
SMX, LLC is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, sexual orientation, age, gender identification, protected veteran status, or any other characteristic protected by law. We consider qualified applicants with arrest and conviction records in accordance with applicable law.
Accommodations are available on request for candidates taking part in the selection process. If you require disability-related accommodation during the recruitment process, please contact your Recruiter or Employee Relations at or . TrueBlue, Inc. and its brands will consult with all applicants who request disability-related accommodation during the recruitment process to ensure that the accommodation provided takes into account the applicant's individual accessibility needs.
SM | SMX is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, sexual orientation, age, gender identification, protected veteran status, or any other characteristic protected by law.

**Position Description**
Looking for a quality inspection opportunity at a fast paced, high impact team? Discover this great opportunity at our Fort Carson, CO location. Bring your expertise to make an impact on our military defense and safety of our soldiers by discovering your new role supporting this critical mission.
This position is contingent upon your ability to maintain your Secret clearance.
Serco supports the US Army as a prime contractor for their Next Generation Command and Control (NGC2) contract which supports integrating capabilities that enable the service to employ Command Posts (CP) across the operational spectrum. Our team develops, integrates, and maintains modern and mobile solutions for an integrated CP infrastructure.
You will be part of a team that works closely with the customer and other Serco functional area teams to deliver quality systems and associated supporting documentation. The team has been recognized by the Army Customer and the industry for their outstanding contributions to the contract and program.
In this role, you will:
+ Visually inspects products according to specifications to ensure conformity to established standards, using a variety of measuring instruments, calipers, micrometers, and gauges
+ Prepare procedures, update and maintain files as needed by ISO certification and quality enhancement
+ Perform first article, piece, in-process as well as final inspections utilizing different automated and manual equipment for inspection
+ Inspect platforms/vehicles to ensure equipment is ready for subsystem integration
+ Maintain accurate records of inspection results, test data, and quality control processes, reporting findings to management
+ A certain degree of creativity and latitude is required. Typically reports to a supervisor or manager
+ Travel is required up to 75+%
Get to know your recruiter: ( be successful in this role, you will have:
+ An active Secret clearance.
+ Bachelor's degree in engineering or technical discipline with 2 years of experience as a product quality control inspector
+ Experience and/or training in: electronics, vehicle operation, electrical wiring, and product assembly.
+ Can read engineering drawings and interconnection diagrams
+ Comfortable standing or walking for long periods of time
+ Ability to use measuring devices like gauges, meters, and calipers.
+ 2 years of demonstrated technical proficiency in Visually inspects products according to specifications to ensure conformity to established standards, using a variety of measuring instruments, calipers, micrometers, and gauges
+ This position is contingent upon your ability to maintain your Secret clearance.
+ Travel is required up to 75+%
Additional desired experience and skills:
+ Understanding of an ISO 9001:2015 QMS system
+ Associate's degree in engineering or technical discipline preferred
+ Physical ability to lift heavy objects.
+ Problem-solving skills
+ Effective written and oral communication skills
+ Familiar with Lean Six Sigma or process improvement concepts
If you are interested in supporting and working with our military and sailors and a passionate Serco team- then submit your application now for immediate consideration. It only takes a few minutes and could change your career!
In compliance with state and local laws regarding pay transparency, the salary range for this role is $55,549.42 to $92,583.07; however, Serco considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate's work experience, education/training, and key skills.
**Company Overview**
Serco Inc. (Serco) is the Americas division of Serco Group, plc. In North America, Serco's 9,000+ employees strive to make an impact every day across 100+ sites in the areas of Defense, Citizen Services, and Transportation. We help our clients deliver vital services more efficiently while increasing the satisfaction of their end customers. Serco serves every branch of the U.S. military, numerous U.S. Federal civilian agencies, the Intelligence Community, the Canadian government, state, provincial and local governments, and commercial clients. While your place may look a little different depending on your role, we know you will find yours here. Wherever you work and whatever you do, we invite you to discover your place in our world. Serco is a place you can count on and where you can make an impact because every contribution matters.
To review Serco benefits please visit: .If you require an accommodation with the application process please email: or call the HR Service Desk at , option 1. Please note, due to EEOC/OFCCP compliance, Serco is unable to accept resumes by email.
Candidates may be asked to present proof of identify during the selection process. If requested, this will require presentation of a government-issued I.D. (with photo) with name and address that match the information entered on the application. Serco will not take possession of or retain/store the information provided as proof of identity. For more information on how Serco uses your information, please see ourApplicant Privacy Policy and Notice ( .
Serco does not accept unsolicited resumes through or from search firms or staffing agencies without being a contracted approved vendor. All unsolicited resumes will be considered the property of Serco and will not be obligated to pay a placement or contract fee. If you are interested in becoming an approved vendor at Serco, please email .
Serco is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
Click here to apply now ( to Serco?**
Join our Talent Community! ( _71056_
**Recruiting Location : Location** _US-CO-Fort Carson_
**Category** _Engineering_
**Position Type** _Full-Time_
**Security Clearance** _Secret_
**Telework** _No - Teleworking not available for this position_

**Position Description**
Looking for a quality inspection opportunity at a fast paced, high impact team? Discover this great opportunity at our Fort Carson, CO location. Bring your expertise to make an impact on our military defense and safety of our soldiers by discovering your new role supporting this critical mission.
This position is contingent upon your ability to maintain your Secret clearance.
Serco supports the US Army as a prime contractor for their Next Generation Command and Control (NGC2) contract which supports integrating capabilities that enable the service to employ Command Posts (CP) across the operational spectrum. Our team develops, integrates, and maintains modern and mobile solutions for an integrated CP infrastructure.
You will be part of a team that works closely with the customer and other Serco functional area teams to deliver quality systems and associated supporting documentation. The team has been recognized by the Army Customer and the industry for their outstanding contributions to the contract and program.
In this role, you will:
+ Supervises and trains Quality Specialist 1 and 2. Typically reports to the Quality Manager"
+ Visually inspects products according to specifications to ensure conformity to established standards, using a variety of measuring instruments, calipers, micrometers, and gauges
+ Prepare procedures, update, and maintain files as needed by ISO certification and quality enhancement.
+ Perform first article, piece, in-process as well as final inspections utilizing different automated and manual equipment for inspection.
+ Inspect platforms/vehicles to ensure equipment is ready for subsystem integration
+ Assist in developing and maintain accurate records of inspection results, test data, and quality control processes, reporting findings to management
+ Review inspection results for trend analysis and root cause analysis to propose corrective actions
+ Works closely with the Production Staff and engineering to maintain smooth operations, verifies lot number and/or serial number traceability of all components, sub-assemblies and finished goods
+ Travel required up to 75+%
Get to know your recruiter: ( be successful in this role, you will have:
+ An active Secret clearance.
+ Requires a Bachelor's degree and 5 years of experienceas a product quality control inspector
+ Experience and/or training in: electronics, vehicle operation, electrical wiring, and product assembly.
+ Can read engineering drawings and interconnection diagrams
+ Comfortable standing or walking for long periods of time
+ Ability to use measuring devices like gauges, meters, and calipers.
+ Demonstrate technical proficiency.
+ Problem-solving skills
+ Effective written and oral communication skills
+ This position is contingent upon your ability to maintain your Secret clearance.
+ Travel required up to 75+%
Additional desired experience and skills:
+ Understanding of an ISO 9001:2015 QMS system
+ Physical ability to lift heavy objects.
+ Familiar with Lean Six Sigma or process improvement concepts
If you are interested in supporting and working with our military and sailors and a passionate Serco team- then submit your application now for immediate consideration. It only takes a few minutes and could change your career!
In compliance with state and local laws regarding pay transparency, the salary range for this role is $67,889.77 to $113,149.62; however, Serco considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate's work experience, education/training, and key skills.
**Company Overview**
Serco Inc. (Serco) is the Americas division of Serco Group, plc. In North America, Serco's 9,000+ employees strive to make an impact every day across 100+ sites in the areas of Defense, Citizen Services, and Transportation. We help our clients deliver vital services more efficiently while increasing the satisfaction of their end customers. Serco serves every branch of the U.S. military, numerous U.S. Federal civilian agencies, the Intelligence Community, the Canadian government, state, provincial and local governments, and commercial clients. While your place may look a little different depending on your role, we know you will find yours here. Wherever you work and whatever you do, we invite you to discover your place in our world. Serco is a place you can count on and where you can make an impact because every contribution matters.
To review Serco benefits please visit: .If you require an accommodation with the application process please email: or call the HR Service Desk at , option 1. Please note, due to EEOC/OFCCP compliance, Serco is unable to accept resumes by email.
Candidates may be asked to present proof of identify during the selection process. If requested, this will require presentation of a government-issued I.D. (with photo) with name and address that match the information entered on the application. Serco will not take possession of or retain/store the information provided as proof of identity. For more information on how Serco uses your information, please see ourApplicant Privacy Policy and Notice ( .
Serco does not accept unsolicited resumes through or from search firms or staffing agencies without being a contracted approved vendor. All unsolicited resumes will be considered the property of Serco and will not be obligated to pay a placement or contract fee. If you are interested in becoming an approved vendor at Serco, please email .
Serco is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
Click here to apply now ( to Serco?**
Join our Talent Community! ( _71059_
**Recruiting Location : Location** _US-CO-Fort Carson_
**Category** _Engineering_
**Position Type** _Full-Time_
**Security Clearance** _Secret_
**Telework** _No - Teleworking not available for this position_

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 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 Newark,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.