Quality Assurance Analyst in Massachusetts

**This role is not eligible for relocation assistance**

Description: Zifo is searching for an experience Quality Assurance Analyst with experience in the pharmaceutical domain. The ideal candidate will have extensive experience with lab instrument qualification. Should be able to go onsite 3 to 4 days a week at Lexington MA.

Requirements

Responsibilities:

• Create and support review of validation life cycle documents for Analytical Instrument Qualification and computerized systems
• Experience in validation of analytical instrument systems (e.g. benchtop analytical systems - spectroscopy, chromatography, protein analyzers, next gen sequencers, PCRs etc.)
• Consult clients on data integrity requirements in Analytical Instruments and perform verification of DI in the systems
• Author validation life cycle documents for client’s review and...

Location: Lexington, MA – ON SITE

**This role will require the successful candidate to be on-site in Lexington, MA**

**This role is not eligible for relocation assistance**

Description: Zifo is searching for an experience Quality Assurance Analyst with experience in the pharmaceutical domain. The ideal candidate will have extensive experience with lab instrument qualification. This role will require a 100% on-site presence in Lexington, MA.

Requirements

Responsibilities:

• Create and support review of validation life cycle documents for Analytical Instrument Qualification and computerized systems
• Experience in validation of analytical instrument systems (e.g. benchtop analytical systems - spectroscopy, chromatography, protein analyzers, next gen sequencers, PCRs etc.)
• Consult clients on data...

Description: Zifo is working with a large pharma client to build a team of QA professionals.

Requirements

Responsibilities:

• Review and approval on change controls, deviations, investigations and CAPAs
• Lead the establishment and maintenance of Quality Agreements
• Provide quality advise and oversight on validation/compliance strategies
• Review and approval of SDLC deliverables
• Review and approval of SOPs, Work Instructions, User Guides, Role Matrices
• Approve vendor qualification documents such as questionnaires, audit reports, and audit responses

Qualifications:

• Bachelor’s/ Master’s degree or equivalent in a scientific or health care field.
• 2-5 years experience as a Technical Consultant, preferably in the pharmaceutical /Life sciences industry preferred.

A successful Zifo-ite...