GMP Investigations Associate — Biopharma IIR
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Pharmaceutical
Regulatory Compliance Specialist -
Quality Assurance - QA/QC
Regulatory Compliance Specialist
Job Description & How to Apply Below
Makro Scientific in Andover, MA is seeking an Investigator Initiated Research Associate to oversee GMP manufacturing investigations. The ideal candidate will have 3-5 years of experience in a quality and compliance setting, with a strong understanding of bio pharmaceutical processes.
This role requires candidates to perform detailed investigations and report generation while adhering to strict quality standards. Relevant educational background in science or engineering is essential.
This opening is for the GMP Investigations Associate — Biopharma IIR role at Makro Scientific.
Full responsibilities and requirements are described in the listing above.
Learn more about the GMP Investigations Associate — Biopharma IIR role in the description above.
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Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).