Demo

Quality Inspector, Senior

Vericel Corporation
Cambridge, MA Full Time
POSTED ON 1/21/2025
AVAILABLE BEFORE 4/19/2025

Job Description

Job Description

This role will be based in our Cambridge, MA location until our new state of the art facility located in Burlington, MA is ready.

Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing Quality Control professional looking to join and contribute to a commercial stage company with an established portfolio of unique advanced cell therapies and specialty biologics. Reporting directly to Quality Control Management at Vericel, this is a great opportunity to join a high growth company with a strong balance sheet supported by a talented team of professionals who are committed to improving the lives of the patients we serve.

POSITION SUMMARY

The individual will be responsible for raw material sampling and inspection internally and at a third-party warehouse. Also responsible for overseeing the inventory of laboratory chemicals and critical reagent supplies across both the Cambridge and Burlington facilities.

DUTIES AND RESPONSIBILITIES

  • Perform inspection, sampling, and release / rejection of components and raw materials as per SOP's and specifications. Individual will monitor various stages of processing along with the appropriate paperwork in compliance with specifications.
  • Collaborate regularly with Supply Chain, QA and Materials Management
  • Partner with outside vendors when required perform inspection and of components and raw materials as well as submitting samples for testing.
  • Support of Quality Control operations by performing basic laboratory responsibilities including environmental monitoring, lab support, inventory of laboratory chemicals and critical reagent supplies, and sample submissions to contract labs.
  • Manage laboratory ordering and inventory management.
  • Update and revise transactions in inventory management system.
  • Flexible and responsive to customer needs.

QUALIFICATIONS, EDUCATION AND EXPERIENCE

  • HS Diploma, 4 years’ industry experience in cGMP, or equivalent.
  • AS Degree, 2-4 years’ industry experience in cGMP, or equivalent
  • BS Degree, 0-2 years’ industry experience in cGMP, or equivalent
  • Direct work experience in a cGMP and pharmaceutical / medical device raw materials quality inspection system.
  • Direct technical experience writing CAPA’s.
  • Preferred Qualifications :

  • Effective time management, multitasking and organizational skills.
  • Strong attention to detail and cross functional team experience.
  • Computer skills in systems such as Microsoft Word, Excel and TrackWise.
  • Knowledge of Laboratory Information Management Systems (LIMS).
  • WORKING CONDITIONS AND PHYSICAL DEMANDS

  • This position will be based in Cambridge MA but will require travel between Cambridge, Burlington MA, and warehouse locations regularly (~50%).
  • Must be able to lift / pull up to 40 pounds.
  • Personal transportation required.
  • Occasional Weekend or Holiday coverage (as needed).
  • Rotating off-shift alarm coverage. May be required to carry a company issued cell phone
  • EEO Statement

    All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. 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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