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Quality AIQ Specialist
- Contract
- Good Distribution Practice (GDP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking a Quality AIQ Specialist to work with a leading pharmaceutical company located in Lexington, MA.
Must be eligible to work or be a citizen in the US.
Job Responsibility:
- Primary duties are focused around the qualification of QC analytical equipment.
- Gap assessment and remediation, equipment classification and release, URS generation, design qualification, computerized system categorization, IOQ protocol and reports, equipment decommissioning, relocation and requalification activities.
- Support QC lab renovation/equipment relocation and equipment qualification activities.
Skills and Requirements:
- Bachelor's Degree in a related discipline and 5 years of related experience.
- Full knowledge of industry GMP and validation practices.
- Experience with ValGenisis, TrackWise, EDMS, compliance, and a strong science and/or validation understanding.
If you are having difficulty in applying or if you have any questions, please contact Tucker Lee at (+1) 215-660-3706 or t.lee@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.
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