Sr QA for Data Integrity, CSV and Analytical Instr. Validation job in Cambridge, USA

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Contract

Discipline: Senior/Director & VP, Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP)

Location: 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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