Specialist GMP Review - Jamaica, VT, United States - Oceanic Ventures
Description
Responsibilities:
- GMP review of electronic manufacturing instructions (Master Batch Records) for batch documentation in biopharmaceutical production (Upstream & Downstream) using BioMES 8 software
- Independent planning and execution of control of electronic manufacturing instructions and accompanying documents
- Maintenance of master data (materials, objects, etc.) in BioMES 8 and SAP
- Administrative tasks such as creating and conducting internal training measures, collecting key figures, training new colleagues, processing change control requests, and preparing for and accompanying audits
Qualifications:
- Bachelor's degree in a natural science field, such as biotechnology, process engineering, chemical engineering, or equivalent, or completed vocational training in a natural science field, such as pharmaceutical technician or chemical technician, with several years of professional experience and possibly further training as a technician or industrial foreman
- Experience in the pharmaceutical industry or other largescale manufacturing plants with a good understanding of production processes
- Strong IT affinity and enjoyment of screenbased tasks
- Experience in a GMP environment
- Good German and English language skills, both written and spoken
- Communication and teamwork skills; independent and precise work style, as well as a high level of initiative
Your contact person:
Sarah Elger, HR Manager,
ecoSPECS GmbH, Hermann-Volz-Str. 56,
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