- Employment
- contract
Employer Job Description
From BioPharma Consulting JAD Group's posting. “We” and “our” refer to the employer.
Own deviations in the Quality Control area at a leading biotechnology company in Juncos, Puerto Rico, as the technical specialist for microbiology and analytical testing.
What you'll do
- Lead and document QC deviations and lab investigations, including root cause and CAPA.
- Provide technical guidance, data analysis and reports across technical groups.
- Resolve technical issues and troubleshoot assays (microbiology, HPLC and analytical methods).
- Develop, revise and audit controlled documents; support lab GMP/GLP compliance and audits.
Requirements
- Bachelor's + 4 years (or Master's + 2, Associate's + 8, High School + 10, or a Doctorate) of directly related experience; microbiology background preferred.
- QC deviations and laboratory investigations in a GMP environment.
- Microbiology, HPLC and analytical methods.
- Strong knowledge of GMPs/CFRs; excellent technical writing.
- Bilingual English/Spanish preferred.
Benefits
- Contract: 5.5 months, with possible extension
- Shift: Administrative, Monday–Friday
About this listing
LAYIQ is an independent job-discovery service. This listing does not imply a partnership with or endorsement by the employer. Review the original posting for current details and availability.
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