Quality Control Analyst: Cell Therapy

Employer
ProClinical
Location
Philadelphia, Pennsylvania
Salary
Negotiable
Posted
Apr 01, 2024
Closes
Apr 04, 2024
Ref
2741888705
Position Type
Analyst
Hours
Hourly
Work Mode
On-site
Employment Type
Contract
Organization Type
Corporation / LLC
Quality Control Analyst: Cell Therapy - Contract - Onsite

Proclinical Staffing is seeking a Quality Control Analyst: Cell Therapy to join a cutting-edge biotech company. This is a contract role located in Philadelphia, PA.

Skills & 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 two 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, changing 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)
  • Experience with cell therapy products

The Quality Control Analyst: Cell Therapy will:
  • Perform daily GMP Quality Control laboratory testing activities 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.
  • Perform all activities with respect to GMP/GDP compliance
  • 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
  • Assist in the 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

Compensation:

$44 hourly

If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at (+1) or .

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.

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