Quality AIQ Specialist

Highly Competitive Salary
  1. Contract
  2. Good Distribution Practice (GDP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
Lexington, MA, USA
Posting date: 22 Feb 2023
QA.TL.52026

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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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