Senior Quality Control Analyst Cell Therapy at Millennium Pharma, Inc.

Posted in General Business 25 days ago.

This job brought to you by eQuest

Type: Full-Time
Location: Cambridge, Massachusetts

Job Description:

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s Privacy Notice, Privacy Policy and Terms of Use.

Job Description

Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda.  Join us as a Senior Quality Control Analyst Cell Therapy in our Cambridge office.

Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Senior Analyst working on the IMP Quality Advanced Therapies team, you will be empowered to support internal QC testing as well as management of contract testing laboratories. and a typical day will include: 


  • The Analyst, Advanced Therapies QC Laboratory is responsible for the performance of testing of cell therapy investigational medicinal products (IMP) utilized in Takeda clinical studies.

  • This position is responsible to assist in start-up activities for the QC laboratory and qualification activities associated with the cGMP cleanrooms (Grade A-C).


  • Perform incoming component/raw material inspection/testing, in-process testing, and product release testing to support the manufacturing of advanced therapy drug products manufactured in the internal GMP facility.

  • Work with contract testing laboratories associated with QC testing for the advanced therapy drug products manufactured at the internal GMP facility.

  • Prepare certificate of analysis of the IMP manufactured at the internal GMP facility.

  • Ensure that testing is performed on time and as needed.

  • Assist in stability testing as needed.

  • Assist in reserve/retention sample and reference sample management.

  • Author, edit, and review SOPs, job aids, reports etc. as assigned.

  • Maintain data integrity and ensure compliance with company SOPs, specifications and cGMP regulations.

  • Assist in the investigation into any non-conformance, OOS, OOT, instrument malfunction, accident or other abnormal occurrence per SOPs.

  • Assist in method transfer and method validation as needed.

  • Assist in testing, managing, data trending and report writing related to stability as needed.

  • Assist in maintenance, calibration and cleaning of QC equipment and instruments as needed.

  • Assist in diverse qualification activities (facility, cleaning, software etc) as needed.

  • Assist in Environmental Monitoring of the internal GMP facility as needed.

  • Assist in the Microbiology laboratory as needed.

  • Keep the QC lab clean, safe and tidy all the times.

  • Work closely and collaboratively with cross-functional team members from QA, QC, production, facility and development.

  • Additional duties as assigned.


Technical/Functional (Line) Expertise

  • Working knowledge of Good Manufacturing Practice requirements.

  • Strong analytical knowledge and practical technical experience with cell therapy methods such as flow cytometry (FACS), q-PCR, cell count methods, and ELISA is a must

  • Experience in raw material sampling and testing

  • Experience writing specifications

  • Experience writing and reviewing SOPs for QC laboratories

  • Experience using a LIMS is a plus


  • Excellent organizational, communication, and interpersonal skills

Decision-making and Autonomy

  • Ability to follow written and verbal directions, as well as carry out testing and tasks independently


  • Experience working in a laboratory

  • Demonstrated ability to collaborate with others


  • Ability to read, analyze and interpret common scientific and technical documents/information

  • Effectively presents information to management, internal groups and stakeholders.


  • Ability to adapt to changing priorities


  • Bachelor’s Degree in Biology or another relevant field

  • Minimum of 5 years’ experience in the bio/pharmaceutical industry

  • Minimum of 3 years’ experience in GMP QC laboratory


  • 401(k) with company match and Annual Retirement Contribution Plan

  • Tuition reimbursement

  • Company match of charitable contributions

  • Health & Wellness programs including onsite flu shots and health screenings

  • Generous time off for vacation and the option to purchase additional vacation days

  • Community Outreach Programs

Empowering Our People to Shine

Learn more at

No Phone Calls or Recruiters Please.



Cambridge, MA

Worker Type


Worker Sub-Type


Time Type

Full time