6,069 Qc Technician jobs in the United States
Quality Control (QC) Technician
63112 Saint Louis, Missouri
Kelly Services
Posted today
Job Viewed
Job Description
**Kelly® Science & Clinical** is seeking a **Quality Control (QC) Technician** for a contract-to-hire (temp-to-permanent, ~6-12 month conversion) position in a clinical laboratory with one of our biotechnology partners in **St. Louis, MO** . Candidates must be currently local to the St. Louis area and able to attend an on-site interview.
If you're passionate about quality and accuracy in the clinical laboratory setting and are ready to take the next step in your career, trust **The Experts at Hiring Experts.**
**Target Pay Rate:** $25-$27/hour.
Pay rate is dependent on relevant experience.
**Location:** St. Louis, MO
**Schedule:** Monday-Friday, 8:00 AM-5:00 PM
**Responsibilities:**
+ Perform **quarantine and release procedures** for critical materials.
+ **Order and manage reagents and materials** for laboratory use.
+ **Investigate temperature and humidity excursions** and document findings.
+ **Review internal installation, maintenance, and calibration records** for compliance.
+ **Prepare and maintain documentation** for periodic review and audits.
+ **Review data and reports** to ensure integrity and accuracy.
+ Promote adherence to **turn-around-time expectations** for sample results.
+ **Collaborate with QA and management** to ensure laboratory operations comply with **ISO 13485** and **CLIA** requirements.
+ **Update and create SOPs, forms, and logs** to reflect current laboratory practices.
+ **Participate in internal and external audits** , ensuring readiness and compliance.
+ **Validate spreadsheets and data tools** used in QC processes.
+ Adhere to all **quality, privacy, and safety standards** required by applicable regulatory agencies.
**Qualifications:**
+ **Bachelor's degree** in Biology, Chemistry, Biochemistry, or a related scientific discipline required.
+ **1-2+ years of experience** in a regulated laboratory environment (ISO 13485, CLIA, or GMP preferred).
+ Strong attention to detail and adherence to established procedures.
+ Excellent documentation, organization, and communication skills.
+ Proficiency with **Microsoft Excel** and general data analysis tools.
+ Ability to work both **independently** and **collaboratively** in a fast-paced environment.
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.
If you're passionate about quality and accuracy in the clinical laboratory setting and are ready to take the next step in your career, trust **The Experts at Hiring Experts.**
**Target Pay Rate:** $25-$27/hour.
Pay rate is dependent on relevant experience.
**Location:** St. Louis, MO
**Schedule:** Monday-Friday, 8:00 AM-5:00 PM
**Responsibilities:**
+ Perform **quarantine and release procedures** for critical materials.
+ **Order and manage reagents and materials** for laboratory use.
+ **Investigate temperature and humidity excursions** and document findings.
+ **Review internal installation, maintenance, and calibration records** for compliance.
+ **Prepare and maintain documentation** for periodic review and audits.
+ **Review data and reports** to ensure integrity and accuracy.
+ Promote adherence to **turn-around-time expectations** for sample results.
+ **Collaborate with QA and management** to ensure laboratory operations comply with **ISO 13485** and **CLIA** requirements.
+ **Update and create SOPs, forms, and logs** to reflect current laboratory practices.
+ **Participate in internal and external audits** , ensuring readiness and compliance.
+ **Validate spreadsheets and data tools** used in QC processes.
+ Adhere to all **quality, privacy, and safety standards** required by applicable regulatory agencies.
**Qualifications:**
+ **Bachelor's degree** in Biology, Chemistry, Biochemistry, or a related scientific discipline required.
+ **1-2+ years of experience** in a regulated laboratory environment (ISO 13485, CLIA, or GMP preferred).
+ Strong attention to detail and adherence to established procedures.
+ Excellent documentation, organization, and communication skills.
+ Proficiency with **Microsoft Excel** and general data analysis tools.
+ Ability to work both **independently** and **collaboratively** in a fast-paced environment.
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.
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0
QC Technician
07676 Township Of Washington, New Jersey
Ultimate Staffing
Posted today
Job Viewed
Job Description
Quality Control (QC) Technician
Schedule: Full-time, 7:00am-4:30pm
Pay Rate: $27.00/hour
Reports to: Quality Manager / Supervisor
Location: Fair Lawn, NJ
Perform inspections and tests on raw materials, in-process products, and finished goods to ensure compliance with company standards and regulatory requirements.
Accurately document results, maintain testing records, and prepare reports for management review.
Assist in identifying, investigating, and reporting quality issues or non-conformances.
Calibrate and maintain laboratory/testing equipment as required.
Support root cause analysis and corrective action processes.
Collaborate with production, operations, and management teams to maintain product quality and safety standards.
Follow established Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMPs), and safety guidelines.
High school diploma or equivalent required; associate or bachelor's degree in a science or technical field preferred.
Previous quality control, laboratory, or manufacturing experience is a plus.
Basic knowledge of quality systems, inspection methods, and industry regulations.
- Must have experience using measuring tools (calipers, micrometers, etc.)
Proficiency in Microsoft Office (Excel, Word, Outlook) and ability to learn company software/databases.
Strong attention to detail, record-keeping, and organizational skills.
Good communication skills and ability to work both independently and in a team environment.'
For more information on this job posting, please text .
All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county , to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.
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1
QC Technician
94587 Willow Creek, California
Adecco US, Inc.
Posted 1 day ago
Job Viewed
Job Description
Hiring Immediately for QC Technician jobs at a local client. Weekly pay starting at $19.00-$1.85 per hour, openings on multiple shifts. Apply now!
+ High School Diploma or GED or AA degree in technical field preferred
+ In absence of high school/GED, candidate should have 3 years (relevant Quality or Lab experience) or 5 years overall experience
+ Experience with MS windows environment: MS Excel, Outlook, PC knowledge
+ Preferred previous QC inspection experience in fast-paced environment
+ Understands, knows, and applies basic knowledge of 5S is a plus
+ Highly attentive to details and numbers
+ Good communication skills; read, write and communicate clearly
+ Dependable attendance
+ Self-motivated and team player
+ Test rotors on instruments according to procedures
+ Perform packaging and final inspection according to procedures
+ Process and save data using PC computer and related tools
+ Report failures and defects to supervisors and troubleshooting staff
+ Complete small projects with minimal supervision
**Pay Details:** 19.00 to 21.85 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.
+ High School Diploma or GED or AA degree in technical field preferred
+ In absence of high school/GED, candidate should have 3 years (relevant Quality or Lab experience) or 5 years overall experience
+ Experience with MS windows environment: MS Excel, Outlook, PC knowledge
+ Preferred previous QC inspection experience in fast-paced environment
+ Understands, knows, and applies basic knowledge of 5S is a plus
+ Highly attentive to details and numbers
+ Good communication skills; read, write and communicate clearly
+ Dependable attendance
+ Self-motivated and team player
+ Test rotors on instruments according to procedures
+ Perform packaging and final inspection according to procedures
+ Process and save data using PC computer and related tools
+ Report failures and defects to supervisors and troubleshooting staff
+ Complete small projects with minimal supervision
**Pay Details:** 19.00 to 21.85 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
QC Technician
01720 Acton, Massachusetts
Teledyne
Posted 1 day ago
Job Viewed
Job Description
**Be visionary**
Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins.
**Job Description**
You will be responsible for conducting thorough inspection of optical components to ensure that they comply with industry standards, customer requirements and regulatory guidelines. As an Inspector at Teledyne Acton Optics, you will be an essential part of our business support team. You will be responsible for ensuring that the incoming materials and products manufactured and supplied meet and exceed customer requirements whilst maintaining quality inspection records.
Key Responsibilities:
+ Perform inspection on incoming material and final product.
+ Complete measurements and detailed inspection to ensure product meet specifications.
+ Maintain detailed records of inspections.
+ Report any non-conformances found during inspections.
+ Assist Quality Manager with resolution of non-conformances and corrective actions.
+ Authority to sign/stamp all release certifications to customer
Other desirable skills and experience include:
+ Ability to read and work from engineering drawings and technical specifications.
+ Experience of measuring parts and components using manual equipment such as: verniers, Calipers, Micrometer, etc
+ Experience using ERP / MRP software, preferably SAP.
+ Strong organizational and time management skills.
+ Attention to detail and a commitment to maintain high accuracy at all times.
Job Knowledge, Skills and Abilities:
+ Ability to work with changing demands in a fast-paced environment
+ Knowledge of MS Office to include Word, Excel, PowerPoint, Outlook
+ Experience in reading technical drawings
+ Experience with Adobe software
+ Product knowledge preferred
+ Quality experience preferred
**Citizenship Requirements**
Due to the type of work at the facility and certain access restrictions, successful applicants must be a U.S. Citizen or Green Card holder.
**_What can Teledyne offer YOU?_**
A Competitive Salary & Benefits Package
Excellent Health, Dental, Vision
Paid Vacation Time
Paid Sick Time
Life Insurance Benefits
Paid Holidays
401(k) Eligibility
Employee Stock Purchase Plan
Educational Tuition Reimbursement
Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions.
Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws.
You may not realize it, but Teledyne enables many of the products and services you use every day **.**
Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.
Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins.
**Job Description**
You will be responsible for conducting thorough inspection of optical components to ensure that they comply with industry standards, customer requirements and regulatory guidelines. As an Inspector at Teledyne Acton Optics, you will be an essential part of our business support team. You will be responsible for ensuring that the incoming materials and products manufactured and supplied meet and exceed customer requirements whilst maintaining quality inspection records.
Key Responsibilities:
+ Perform inspection on incoming material and final product.
+ Complete measurements and detailed inspection to ensure product meet specifications.
+ Maintain detailed records of inspections.
+ Report any non-conformances found during inspections.
+ Assist Quality Manager with resolution of non-conformances and corrective actions.
+ Authority to sign/stamp all release certifications to customer
Other desirable skills and experience include:
+ Ability to read and work from engineering drawings and technical specifications.
+ Experience of measuring parts and components using manual equipment such as: verniers, Calipers, Micrometer, etc
+ Experience using ERP / MRP software, preferably SAP.
+ Strong organizational and time management skills.
+ Attention to detail and a commitment to maintain high accuracy at all times.
Job Knowledge, Skills and Abilities:
+ Ability to work with changing demands in a fast-paced environment
+ Knowledge of MS Office to include Word, Excel, PowerPoint, Outlook
+ Experience in reading technical drawings
+ Experience with Adobe software
+ Product knowledge preferred
+ Quality experience preferred
**Citizenship Requirements**
Due to the type of work at the facility and certain access restrictions, successful applicants must be a U.S. Citizen or Green Card holder.
**_What can Teledyne offer YOU?_**
A Competitive Salary & Benefits Package
Excellent Health, Dental, Vision
Paid Vacation Time
Paid Sick Time
Life Insurance Benefits
Paid Holidays
401(k) Eligibility
Employee Stock Purchase Plan
Educational Tuition Reimbursement
Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions.
Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws.
You may not realize it, but Teledyne enables many of the products and services you use every day **.**
Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.
View Now
3
QC Technician
07308 Jersey City, New Jersey
System One
Posted today
Job Viewed
Job Description
Job Title: QC Technician
Location: Jersey City, NJ (On-site)
Type: Contract-to-Hire (4 months)
Compensation: $31-$3/hr (Contract) | 65,000- 70,000/year (Conversion Salary)
Schedule: Monday-Friday, 9:00 AM - 5:00 PM
Start Date: Immediate or within 2 weeks
About the Role
A growing medical device company in Jersey City, NJ is seeking a Quality Control (QC) Technician to support day-to-day laboratory operations in a GMP-regulated manufacturing environment. This role includes hands-on testing of raw materials and finished products, cleanroom environmental monitoring, and lab equipment calibration to ensure compliance with FDA and ISO 13485 standards.
This is a 4-month contract-to-hire opportunity with the potential for full-time conversion - or direct hire for the right candidate.
Key Responsibilities
+ Perform analytical testing on raw materials, in-process samples, and finished products per SOPs and GMP guidelines
+ Conduct LAL (Limulus Amebocyte Lysate) testing for endotoxin detection
+ Execute environmental monitoring in classified cleanroom areas (viable and non-viable particulates)
+ Support validation testing activities and accurately document results
+ Coordinate calibration and maintenance of lab and production instruments
+ Participate in deviation, OOS, and CAPA investigations
Qualifications
+ Associate's or Bachelor's degree in Biology, Chemistry, Microbiology, or related field
+ 1-3 years of hands-on QC experience in medical device, pharmaceutical, or biotech manufacturing preferred
+ Familiarity with LAL testing, environmental monitoring, and analytical techniques (e.g. pH, conductivity)
+ Working knowledge of GMP, GLP, FDA QSR, and ISO 13485 regulations
+ Strong attention to detail, documentation accuracy, and time management
+ Proficiency with Microsoft Office; experience with LIMS is a plusWhy Apply?
+ Opportunity to work in a regulated, impact-driven environment
+ Gain valuable experience in GMP and ISO 13485-compliant QC operations
+ Potential to convert to a full-time role or direct hire based on performance
+ Ensure audit readiness and uphold quality and safety standards
+ Contribute to continuous improvement initiatives within the quality system testing for endotoxin detection
+ Execute environmental monitoring in classified cleanroom areas (viable and non-viable particulates)
+ Support validation testing activities and accurately document results
+ Coordinate calibration and maintenance of lab and production instruments
+ Participate in deviation, OOS, and CAPA investigations
+ Ensure audit readiness and uphold quality and safety standards
+ Contribute to continuous improvement initiatives within the quality system
Why Apply?
+ Opportunity to work in a regulated, impact-driven environment
+ Gain valuable experience in GMP and ISO 13485-compliant QC operations
+ Potential to convert to a full-time role or direct hire based on performance
System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M-
#LI-
#DI-
Ref: #558-Scientific
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
Location: Jersey City, NJ (On-site)
Type: Contract-to-Hire (4 months)
Compensation: $31-$3/hr (Contract) | 65,000- 70,000/year (Conversion Salary)
Schedule: Monday-Friday, 9:00 AM - 5:00 PM
Start Date: Immediate or within 2 weeks
About the Role
A growing medical device company in Jersey City, NJ is seeking a Quality Control (QC) Technician to support day-to-day laboratory operations in a GMP-regulated manufacturing environment. This role includes hands-on testing of raw materials and finished products, cleanroom environmental monitoring, and lab equipment calibration to ensure compliance with FDA and ISO 13485 standards.
This is a 4-month contract-to-hire opportunity with the potential for full-time conversion - or direct hire for the right candidate.
Key Responsibilities
+ Perform analytical testing on raw materials, in-process samples, and finished products per SOPs and GMP guidelines
+ Conduct LAL (Limulus Amebocyte Lysate) testing for endotoxin detection
+ Execute environmental monitoring in classified cleanroom areas (viable and non-viable particulates)
+ Support validation testing activities and accurately document results
+ Coordinate calibration and maintenance of lab and production instruments
+ Participate in deviation, OOS, and CAPA investigations
Qualifications
+ Associate's or Bachelor's degree in Biology, Chemistry, Microbiology, or related field
+ 1-3 years of hands-on QC experience in medical device, pharmaceutical, or biotech manufacturing preferred
+ Familiarity with LAL testing, environmental monitoring, and analytical techniques (e.g. pH, conductivity)
+ Working knowledge of GMP, GLP, FDA QSR, and ISO 13485 regulations
+ Strong attention to detail, documentation accuracy, and time management
+ Proficiency with Microsoft Office; experience with LIMS is a plusWhy Apply?
+ Opportunity to work in a regulated, impact-driven environment
+ Gain valuable experience in GMP and ISO 13485-compliant QC operations
+ Potential to convert to a full-time role or direct hire based on performance
+ Ensure audit readiness and uphold quality and safety standards
+ Contribute to continuous improvement initiatives within the quality system testing for endotoxin detection
+ Execute environmental monitoring in classified cleanroom areas (viable and non-viable particulates)
+ Support validation testing activities and accurately document results
+ Coordinate calibration and maintenance of lab and production instruments
+ Participate in deviation, OOS, and CAPA investigations
+ Ensure audit readiness and uphold quality and safety standards
+ Contribute to continuous improvement initiatives within the quality system
Why Apply?
+ Opportunity to work in a regulated, impact-driven environment
+ Gain valuable experience in GMP and ISO 13485-compliant QC operations
+ Potential to convert to a full-time role or direct hire based on performance
System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M-
#LI-
#DI-
Ref: #558-Scientific
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
View Now
4
QC Technician
08701 Leisure Village East, New Jersey
System One
Posted today
Job Viewed
Job Description
Job Title: QC Technician
Location: Lakewood, NJ
Type: Contract To Hire
Compensation: $25 - $27 hourly
Contractor Work Model: Onsite
Hours: 7 AM- 3:30 PM M-F
Responsibilities:
Evaluate products, raw materials and intermediates for conformance to specifications and comply with all Quality Assurance standards that are in place.
+ Perform daily evaluation and approval of finished products, raw materials, and intermediates. This would include FPY / OAC and extended performance testing (7 days).
+ Perform production line first-piece inspection and production floor spot checks, as needed.
+ Work as team member with other employees to ensure timely reporting of results so quality products can ship, and bad quality products don't go out.
+ Report and record all results in a timely manner. Maintain a proper database with detailed testing results and generate appropriate statistical analyses via use of a computer and SAP.
+ Able and willing to effectively communicate, share information, give, and receive constructive feedback in a respectful and professional manner.
+ Make any notations and bring them to the attention of R&D / Operations of inspection plans that need updating whether it is control limit shifts or additional testing.
+ Create COA's for customers in a timely fashion.
+ Perform all tests timely, accurately, and responsibly by signing all conforming reports and alerting Plant Management and Production Management of non-conformances.
+ Offer ideas and plans for improvement as well as point out deficiencies in the laboratory, especially in the areas of specifications and procedures.
+ Maintain and be responsible for the working inventory of all lab supplies and chemicals you use.
+ Accurately calibrate, control, and maintain lab instruments.
+ Perform test results analysis in Excel and input/update SAP quality information.
+ Stay current with new automation, technology, mechanical equipment, and computer software programs.
+ Provide timely results of non-routine samples, for example, when looking into customer complaints.
+ May perform other projects or assignments as required.
+ Maintain good housekeeping and performs minor maintenance of equipment, workstation, and lab area.
+ Responsible for monitoring the accuracy and completeness of all process instructions and in process quality checks assuring compliance with S.O.P.
Requirements:
+ 3+ years hand-on experiences in a laboratory environment or 3+ years QA/QC experience.
+ ASTM/ISO experience
+ High School diploma or equivalent.
+ Strong attention to detail.
+ Ability to manage tasks and responsibilities to complete priorities in a timely manner.
+ Strong customer and quality focus.
+ Ability to work in a team environment
System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M-
#LI-
#DI-
Ref: #558-Scientific
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
Location: Lakewood, NJ
Type: Contract To Hire
Compensation: $25 - $27 hourly
Contractor Work Model: Onsite
Hours: 7 AM- 3:30 PM M-F
Responsibilities:
Evaluate products, raw materials and intermediates for conformance to specifications and comply with all Quality Assurance standards that are in place.
+ Perform daily evaluation and approval of finished products, raw materials, and intermediates. This would include FPY / OAC and extended performance testing (7 days).
+ Perform production line first-piece inspection and production floor spot checks, as needed.
+ Work as team member with other employees to ensure timely reporting of results so quality products can ship, and bad quality products don't go out.
+ Report and record all results in a timely manner. Maintain a proper database with detailed testing results and generate appropriate statistical analyses via use of a computer and SAP.
+ Able and willing to effectively communicate, share information, give, and receive constructive feedback in a respectful and professional manner.
+ Make any notations and bring them to the attention of R&D / Operations of inspection plans that need updating whether it is control limit shifts or additional testing.
+ Create COA's for customers in a timely fashion.
+ Perform all tests timely, accurately, and responsibly by signing all conforming reports and alerting Plant Management and Production Management of non-conformances.
+ Offer ideas and plans for improvement as well as point out deficiencies in the laboratory, especially in the areas of specifications and procedures.
+ Maintain and be responsible for the working inventory of all lab supplies and chemicals you use.
+ Accurately calibrate, control, and maintain lab instruments.
+ Perform test results analysis in Excel and input/update SAP quality information.
+ Stay current with new automation, technology, mechanical equipment, and computer software programs.
+ Provide timely results of non-routine samples, for example, when looking into customer complaints.
+ May perform other projects or assignments as required.
+ Maintain good housekeeping and performs minor maintenance of equipment, workstation, and lab area.
+ Responsible for monitoring the accuracy and completeness of all process instructions and in process quality checks assuring compliance with S.O.P.
Requirements:
+ 3+ years hand-on experiences in a laboratory environment or 3+ years QA/QC experience.
+ ASTM/ISO experience
+ High School diploma or equivalent.
+ Strong attention to detail.
+ Ability to manage tasks and responsibilities to complete priorities in a timely manner.
+ Strong customer and quality focus.
+ Ability to work in a team environment
System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M-
#LI-
#DI-
Ref: #558-Scientific
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
View Now
5
QC Technician
63112 Saint Louis, Missouri
Actalent
Posted 14 days ago
Job Viewed
Job Description
QC Technician
Job Description
We are seeking dedicated QC Technicians for two open positions, with shifts from 7am-7pm and 7pm-7am. As a QC Technician, you will spend nearly all your time on the production floor, documenting data and non-conformances using computers stationed alongside the production lines. Your primary responsibility is to identify any products that do not meet specifications and escalate these issues to the QA Lead. You will also conduct visual inspections to ensure products have clear labels and bar codes.
Responsibilities
+ Understand and demonstrate safe work practices at all times.
+ Monitor the statistical process control (SPC) software suite, Gainseeker.
+ Monitor, measure, and document line processes to ensure compliance with product specifications.
+ Examine and document packaging components and finished product assembly for conformity to specifications.
+ Program, calibrate, and assist in setting up Hi-Speed check weighers, Videojet, and Marsh coders.
+ Monitor the Automated Inventory Management system for tracking finished production.
+ Place non-conforming products on hold for QC Manager's review.
+ Pull and retain product samples.
+ Comply with all company policies and procedures.
+ Perform other duties as assigned.
Essential Skills
+ Experience with GMP, quality inspection, GMP/FDA regulations.
+ Proficient in Quality, Laboratory, Quality Assurance, QC, Document Control.
+ Experience in regulated environments, regulatory compliance, and batch record management.
+ Proficiency in Microsoft Office, quality checks, and SOPs.
Additional Skills & Qualifications
+ Interest in the industry and willingness to learn.
+ Experience in a regulated or Quality Control environment preferred.
+ Strong attention to detail and pride in work.
+ Basic math skills for quick determinations.
+ Soft skills including a strong interest in learning and taking on new responsibilities.
Work Environment
The role involves spending almost 100% of the time in the plant, with occasional lab work. The technician will primarily be on their feet conducting inspections. This position offers exposure to various instruments and cutting-edge products in the pesticide and home protection manufacturing business. Opportunities for promotion exist as the company continues to grow.
Pay and Benefits
The pay range for this position is $18.25 - $18.25/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 St. Louis,MO.
Application Deadline
This position is anticipated to close on Oct 1, 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 dedicated QC Technicians for two open positions, with shifts from 7am-7pm and 7pm-7am. As a QC Technician, you will spend nearly all your time on the production floor, documenting data and non-conformances using computers stationed alongside the production lines. Your primary responsibility is to identify any products that do not meet specifications and escalate these issues to the QA Lead. You will also conduct visual inspections to ensure products have clear labels and bar codes.
Responsibilities
+ Understand and demonstrate safe work practices at all times.
+ Monitor the statistical process control (SPC) software suite, Gainseeker.
+ Monitor, measure, and document line processes to ensure compliance with product specifications.
+ Examine and document packaging components and finished product assembly for conformity to specifications.
+ Program, calibrate, and assist in setting up Hi-Speed check weighers, Videojet, and Marsh coders.
+ Monitor the Automated Inventory Management system for tracking finished production.
+ Place non-conforming products on hold for QC Manager's review.
+ Pull and retain product samples.
+ Comply with all company policies and procedures.
+ Perform other duties as assigned.
Essential Skills
+ Experience with GMP, quality inspection, GMP/FDA regulations.
+ Proficient in Quality, Laboratory, Quality Assurance, QC, Document Control.
+ Experience in regulated environments, regulatory compliance, and batch record management.
+ Proficiency in Microsoft Office, quality checks, and SOPs.
Additional Skills & Qualifications
+ Interest in the industry and willingness to learn.
+ Experience in a regulated or Quality Control environment preferred.
+ Strong attention to detail and pride in work.
+ Basic math skills for quick determinations.
+ Soft skills including a strong interest in learning and taking on new responsibilities.
Work Environment
The role involves spending almost 100% of the time in the plant, with occasional lab work. The technician will primarily be on their feet conducting inspections. This position offers exposure to various instruments and cutting-edge products in the pesticide and home protection manufacturing business. Opportunities for promotion exist as the company continues to grow.
Pay and Benefits
The pay range for this position is $18.25 - $18.25/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 St. Louis,MO.
Application Deadline
This position is anticipated to close on Oct 1, 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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6
Sr. QC Technician
02762 Plainville, Massachusetts
ThermoFisher Scientific
Posted today
Job Viewed
Job Description
**Work Schedule**
10 hr shift/days
**Environmental Conditions**
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.)
**Job Description**
Analyst I, QC Microbiology
Thermo Fisher Scientific's Viral Vector Services (VVS) is a rapidly growing, gene therapy contract development and manufacturing organization (CDMO) that is seeking sharp individuals to bring the highest quality processes, products and testing to our clients. Our employees are committed to making a difference in our organization, for our client partners and the patients we serve. We are looking for top talent with proven competencies and strong character to join our team and help lead our organization into the future.
Location
Plainville, MA
How will you make an impact
The Associate will complete microbiology assays such as bioburden, endotoxin, and growth promotion. The incumbent will also support equipment, documentation, investigations and improvement initiatives within QC Microbiology. Works cohesively with peers and QC Microbiology management.
What will you do?
Performs routine environmental monitoring and critical utility sampling, routine microbiology assays, growth promotion, and method suitability testing.
Performs inventory and stocking of QC lab.
Reviews data and enter results into LIMS system
Performs routine laboratory preventative maintenance and cleaning
Investigates alert and action level results, as well as support deviation initiation and writing
Provides data to external departments to facilitate investigation closure, support action notice sampling, investigative sampling when required, as well as isolator sampling
Train junior analysts!
Drafts and revises technical documents (SOPs, Work Instructions) and assist with continually improving on the job training
Special Requirements
Ability to gown and gain access to cleanroom and utility areas
Position requires frequent bending, stooping, standing, and ability to lift 40lbs
Ability to work with strong chemical odors such as Spor-Klenz or bleach
Position is considered essential personnel and may be required to staff the lab during inclement weather or other internal/external emergency situations
Rotating holiday coverage
Occasional off shift hours may be required to meet business needs
How will you get here?
Education
Bachelor's degree in biological sciences
Experience
0-1 years of industry experience performing environmental monitoring, critical utility and microbiological assays
At Thermo Fisher Scientific, each one of our 70,000 outstanding minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
10 hr shift/days
**Environmental Conditions**
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.)
**Job Description**
Analyst I, QC Microbiology
Thermo Fisher Scientific's Viral Vector Services (VVS) is a rapidly growing, gene therapy contract development and manufacturing organization (CDMO) that is seeking sharp individuals to bring the highest quality processes, products and testing to our clients. Our employees are committed to making a difference in our organization, for our client partners and the patients we serve. We are looking for top talent with proven competencies and strong character to join our team and help lead our organization into the future.
Location
Plainville, MA
How will you make an impact
The Associate will complete microbiology assays such as bioburden, endotoxin, and growth promotion. The incumbent will also support equipment, documentation, investigations and improvement initiatives within QC Microbiology. Works cohesively with peers and QC Microbiology management.
What will you do?
Performs routine environmental monitoring and critical utility sampling, routine microbiology assays, growth promotion, and method suitability testing.
Performs inventory and stocking of QC lab.
Reviews data and enter results into LIMS system
Performs routine laboratory preventative maintenance and cleaning
Investigates alert and action level results, as well as support deviation initiation and writing
Provides data to external departments to facilitate investigation closure, support action notice sampling, investigative sampling when required, as well as isolator sampling
Train junior analysts!
Drafts and revises technical documents (SOPs, Work Instructions) and assist with continually improving on the job training
Special Requirements
Ability to gown and gain access to cleanroom and utility areas
Position requires frequent bending, stooping, standing, and ability to lift 40lbs
Ability to work with strong chemical odors such as Spor-Klenz or bleach
Position is considered essential personnel and may be required to staff the lab during inclement weather or other internal/external emergency situations
Rotating holiday coverage
Occasional off shift hours may be required to meet business needs
How will you get here?
Education
Bachelor's degree in biological sciences
Experience
0-1 years of industry experience performing environmental monitoring, critical utility and microbiological assays
At Thermo Fisher Scientific, each one of our 70,000 outstanding minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
View Now
7
QC Technician II
66219 Lenexa, Kansas
ThermoFisher Scientific
Posted 1 day ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Laboratory Setting
**Job Description**
**Job Description**
**Job Title:** Quality Control Technician II
Reports To: Quality Control Supervisor
Group/Division: SDG/MBD
Career Band: Band 2
Job Track: Associate
Position Location: Lenexa Kansas
Number of Direct Reports none
Day/Shift (if applicable): Monday - Thursday , 7am - 5:30pm Schedule may be flexed to a Tuesday - Friday 7am - 5:30pm based on Laboratory needs.
FLSA Status (Exempt/Non-Exempt): Non-Exempt
**Position Summary:**
Responsible for the evaluation of quality control samples through physical evaluation and microbial load testing of plated and non-plated media, control of documents, and maintaining good general laboratory practices.
**Key Responsibilities:**
+ Review and maintain product compliance specifications, documentation control.
+ Gain proficiency on all testing areas.
+ Documentation of testing results and determination of aesthetic quality on finished product.
+ Maintain consistency for training tasks in Master Control.
+ Maintain SOP criteria for inspection/testing.
+ Responsible for maintaining department equipment and ordering consumable stock supplies when vital.
+ Exercise GMP and GLP compliance in work environment.
+ Work well in a high volume fast paced environment.
+ Work closely with Quality Assurance department as a quality team.
+ Work with the continuous improvement program within the department.
+ Understand and exercise all safety requirements and procedures.
+ Assists in maintaining standards in accordance with GMP's/SOP's and ISO regulations.
+ Accomplish department goals.
+ Support all company policies.
+ Performs other duties as assigned.
**Minimum Requirements/Qualifications:**
+ Possess a high school diploma or equivalent.
+ Some laboratory experience in a biological sciences laboratory is preferred.
+ A minimum combined 1-2 years of experience of in related QC/QA, microbiology laboratory work in a laboratory setting, or an equivalent combination of education and experience is a plus.
+ Some familiarity with FDA regulations for medical devices.
+ Possess the ability to manage many tasks and in an organized fashion.
+ Possess intermediate computer skills, preferably with experience in Microsoft word to include Word, Excel and PowerPoint programs. Experience working in SAP is a plus.
+ Listen to, and follow, written and verbal instructions in English.
+ Able to adapt and to learn new procedures and to maintain a scientific and objective approach.
+ Must be available to work alternate shifts when needed.
+ Must maintain a professional workplace attitude.
+ Self-motivated, highly responsible and possess a good teamwork spirit.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Laboratory Setting
**Job Description**
**Job Description**
**Job Title:** Quality Control Technician II
Reports To: Quality Control Supervisor
Group/Division: SDG/MBD
Career Band: Band 2
Job Track: Associate
Position Location: Lenexa Kansas
Number of Direct Reports none
Day/Shift (if applicable): Monday - Thursday , 7am - 5:30pm Schedule may be flexed to a Tuesday - Friday 7am - 5:30pm based on Laboratory needs.
FLSA Status (Exempt/Non-Exempt): Non-Exempt
**Position Summary:**
Responsible for the evaluation of quality control samples through physical evaluation and microbial load testing of plated and non-plated media, control of documents, and maintaining good general laboratory practices.
**Key Responsibilities:**
+ Review and maintain product compliance specifications, documentation control.
+ Gain proficiency on all testing areas.
+ Documentation of testing results and determination of aesthetic quality on finished product.
+ Maintain consistency for training tasks in Master Control.
+ Maintain SOP criteria for inspection/testing.
+ Responsible for maintaining department equipment and ordering consumable stock supplies when vital.
+ Exercise GMP and GLP compliance in work environment.
+ Work well in a high volume fast paced environment.
+ Work closely with Quality Assurance department as a quality team.
+ Work with the continuous improvement program within the department.
+ Understand and exercise all safety requirements and procedures.
+ Assists in maintaining standards in accordance with GMP's/SOP's and ISO regulations.
+ Accomplish department goals.
+ Support all company policies.
+ Performs other duties as assigned.
**Minimum Requirements/Qualifications:**
+ Possess a high school diploma or equivalent.
+ Some laboratory experience in a biological sciences laboratory is preferred.
+ A minimum combined 1-2 years of experience of in related QC/QA, microbiology laboratory work in a laboratory setting, or an equivalent combination of education and experience is a plus.
+ Some familiarity with FDA regulations for medical devices.
+ Possess the ability to manage many tasks and in an organized fashion.
+ Possess intermediate computer skills, preferably with experience in Microsoft word to include Word, Excel and PowerPoint programs. Experience working in SAP is a plus.
+ Listen to, and follow, written and verbal instructions in English.
+ Able to adapt and to learn new procedures and to maintain a scientific and objective approach.
+ Must be available to work alternate shifts when needed.
+ Must maintain a professional workplace attitude.
+ Self-motivated, highly responsible and possess a good teamwork spirit.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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8