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Quality Control Analyst, I

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Cambridge

On-site

GBP 25,000 - 45,000

Full time

20 days ago

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Job summary

Join a pioneering organization in regenerative medicine as a Quality Control Analyst I, where you will play a crucial role in ensuring the quality of groundbreaking therapies. This position involves performing routine testing and analysis of raw materials and drug products, contributing to the development of innovative treatments that transform patient care. You'll work in a collaborative environment, gaining valuable experience in a cGMP laboratory setting while supporting a mission-driven team dedicated to improving lives. If you are passionate about science and quality assurance, this opportunity is perfect for you.

Benefits

Career Growth Opportunities
Collaborative Culture
Cutting-Edge Science Exposure

Qualifications

  • Experience in a cGMP lab environment is essential.
  • Proficiency in Microsoft Office and lab data management systems required.

Responsibilities

  • Perform routine QC testing of raw materials and drug products.
  • Assist in reviewing QC data and reporting results.
  • Maintain laboratory equipment and ensure compliance with SOPs.

Skills

Microbiological Testing
Environmental Monitoring
Problem Solving
Data Management Systems (LIMs)
cGMP Regulations Knowledge

Education

High School Diploma
Associate's Degree in Microbiology
Bachelor's Degree in a Related Discipline

Tools

Balances
Pipettes
pH Meter
UV/Visible Spectrophotometer
Plate Reader

Job description

Job Description

At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care).

Position Summary:

The Quality Control Analyst I is responsible for performing routine testing of raw materials, in-process, drug product (DP) and stability samples within the QC laboratory in accordance with SOPs for product release and validation.

Schedule: As a company that thrives on teamwork and collaboration, this role will be required to work on-site 5 days per week: Tuesday-Saturday.

Position Scope:

  1. Perform routine QC testing for raw materials, in-process, DP, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, plate reader, etc. in accordance with SOPs and cGMP guidelines.
  2. Perform cell culture microbial and/or molecular assays.
  3. Perform routine Environmental Monitoring and utilities testing.
  4. Perform microbial limits, Bioburden testing, and identifying and trending microorganisms.
  5. Lab support including but not limited to glass washing, autoclaving, etc.
  6. Assist in the review of QC data and provide summaries to management as needed.
  7. Report out-of-specification or out-of-trend results in a timely manner to ensure appropriate actions are taken.
  8. Performance of QC general laboratory equipment calibration and maintenance, laboratory housekeeping and preparation of the laboratory for audits.
  9. Participate in transfer methods from support groups to the QC laboratory.
  10. Coordinate departmental systems (i.e. inventory, documentation, equipment maintenance).
  11. Communicate inter-departmentally and with outside contacts to solve technical issues.
  12. Exercise sound judgment and decision making when problem solving.
  13. Author and conduct periodic review to QC documents, including SOPs, protocols and forms as needed.
  14. Initiate deviations and lab investigations as needed.
  15. Practice safe work habits and adhere to Vericel’s safety procedures and guidelines.
  16. Other duties as assigned.

Qualifications:

  1. HS Diploma with 4+ years’ industry experience in cGMP lab environment, or
  2. Associate’s degree in microbiology, molecular biology, biochemistry or a related discipline plus 2-4 years’ industry experience or
  3. Bachelor’s degree with 0-2 years’ industry experience in cGMP lab environment.
  4. Basic working knowledge of cGMP regulations.
  5. Proficiency in Outlook, MS Word, Excel and lab based data management systems (LIMs).
  6. Experience with microbiological testing or environmental monitoring.
  7. Experience in biotech, pharmaceutical or other regulated industry.
  8. Ability to lift 40 lbs.
  9. Required to work one day per weekend.
  10. Ability to work rotating holiday coverage.
  11. May carry company issued cell phone for off-shift remote alarm coverage.
  12. Required to gown into classified manufacturing ISO 7 clean room areas.

Why Vericel?

  1. Cutting-Edge Science: Work with a leading regenerative medicine product that is transforming patient care.
  2. Career Growth: Be a part of a growing organization with opportunities to expand your impact.
  3. Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives.

EEO Statement

All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, age, disability, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of . Vericel Corporation is an Equal Opportunity/Affirmative Action Employer.

Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.

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