Similar posts
Quality Control Analyst, Cell Therapy
- Contract
- Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking a Quality Control Analyst, Cell Therapy for a biopharmaceutical startup located in Philadelphia, PA. This individual will support the ramp up of QC and other activities in a newly built facility for cell therapy products.
Must be eligible to work in the US.
Job Responsibilities:
- Perform daily GMP Quality Control laboratory testing activities at the iCTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations
- Perform data analysis and final result reporting to support product lot release with adherence to turnaround times.
- Support thorough GMP investigations for out of specification test results and other quality events
- Support technical problem solving for issues pertaining to GMP Quality Control
- Support product stability programs including execution of stability testing, stability data analysis and trending, and final reporting of stability data
- Support generation and revisions of documentation, such as SOP, protocols and reports, deviations, laboratory investigations, CAPAs and change controls
- Perform peer review of laboratory data and logbooks
- Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results
- Support Health Authority inspections
- Provide input to functional laboratory team meetings
- Other responsibilities as assigned
Skills and Requirements:
- Bachelor's degree in a relevant discipline (biological sciences or equivalent).
- Minimum three (3) years of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus
- Experience with one or more of the following: Flow Cytometry, Cell based ELISA, NC200
- Successfully interface with multi-disciplined teams
- Extremely detail-oriented with strong technical skills.
- Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity
- High level of ownership and accountability
- Demonstrate sense of urgency; ability to recognize time sensitivity
- Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint)
If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at (+1) 267-428-7770 or m.raletz@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#LI-MR2
INDCQA
Related jobs
Highly Competitive
Stein, Schweiz
Join a leading Swiss sterile manufacturing operation as a Sr. Quality Assurance Expert driving GMP excellence, operational partnership, and continuous quality improvement.
Highly Competitive
Philadelphia, USA
Drive the quality systems that keep GMP operations compliant, efficient, and audit‑ready.
Highly Competitive
Philadelphia, USA
Ensure GMP excellence by owning the accuracy, integrity, and compliance of critical quality documentation.
Highly Competitive
Waltham, USA
Keep quality on track and inspection‑ready by owning the systems that keep operations running smoothly.
Highly Competitive
Birmingham, USA
Be the quality gatekeeper who keeps patients safe and products flawless.
Highly Competitive
Rockville, USA
Step into a role where precision meets purpose-become a Materials Technician supporting essential pharma and respiratory operations
Highly Competitive
Liverpool, England
Are you passionate about quality and precision? Join our client in this Quality Assurance Representative and help ensure top-tier standards every day.