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Sr QA for Data Integrity, CSV and Analytical Instr. Validation
- Contract
- Senior/Director & VP, Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP)
- United States
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 j.cerchio@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.
INDCQA
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