Sr QA for Data Integrity, CSV and Analytical Instr. Validation

Highly Competitive Salary
  1. Contract
  2. Senior/Director & VP, Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP)
  3. United States
Cambridge, USA
Posting date: 04 Dec 2023

This vacancy has now expired. Please see similar roles below...

Proclinical is seeking a hybrid Senior QA for Data Integrity, CSV and Analytical Instruments Validation to join a global biopharmaceutical company located in Cambridge, MA.

Must be eligible to work in the US.

Job Responsibilities:

  • Provide QA oversight and Strategic leadership of the Data Integrity program, Computer validation and Lab Instruments validation at the site.
  • Define, drive, manage, implement, integrate and remediate the Data Integrity program.
  • Ensure compliance with all regulatory requirements relating to Data Integrity.
  • Review and approve project plans, SIA's, URS's, DQ's, RA's, Validation protocols, Summary reports, SOPs, Specifications, and other applicable validation documentation.
  • Need to be experts on Data Integrity

Skills and Requirements:

  • 10+ years of industry experience, with in depth knowledge of data integrity requirements, Computer validation, and Lab Instruments Validation
  • Commitment to Quality
  • Excellent written and oral presentation skills
  • 3 days onsite

If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 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.