Quality Systems Specialist job in La Verne, USA

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: United States

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

Proclinical is currently recruiting for a Quality Systems Specialist position located in the La Verne, CA area with one of the world's leading pharmaceutical companies. A successful candidate will have laboratory experience, performs thorough reviews of raw data and documentation to ensure compliance to applicable specifications and protocols, advanced knowledge of current Good Manufacturing Practices (GMPs), and supports OOS/OOT investigation and CAPA implementation.

Job Responsibilities:

Primary responsibilities of the job are to review the data and execution of vendor protocols for instrument qualifications.
May also author qualification documents (URS, protocols, reports, etc.).
Provide support for qualification maintenance activities of QC instruments and equipment.
Review of vendor executed protocols and reports.

Skills and Requirements:

MA/MS or PhD preferred.
Experience in a laboratory setting ideally with some instrument qualification experience and data review experience.
Experience with a laboratory is required.
GMP laboratory experience is preferred.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Catherine Nguyen at (+1) 215-531-5643 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

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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