Job Description
Crystal Pharmatech Inc. - Cranbury, NJ, USA
Job Description
The Quality Assurance Specialist will report to the Head of Small Molecule Division. The candidate will be in charge of all quality assurance activities at the site, including maintenance of the SOPs, site preparation for client audits, review of GMP data, quality training of the R&D personnel. Maximum of 5 work hours per day is required. This is a contractor position with possibility of converting to a part-time employee on business needs.
The ideal candidate should have the following qualifications:
Roles and Responsibilities
· Maintenance of the QMS:
o SOP periodic review
o Change control
o Instruments IQ/OQ
o Quality training of the R&D personnel.
o Site preparation for client’s audits
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