- Experience
- 8+ yrs
- Location
- Grand Rapids, Michigan, United States
- Job type
- Full-time
About the role
Bachelor's degree in Life Sciences or related field and/or 8+ years related experience; 3+ years technical writing with quality investigations, root cause analysis, CAPA; knowledge of cGMP, FDA and multinational regulations; client-facing experience.
About Grand River Aseptic Manufacturing
Private pharmaceutical CDMO producing sterile injectable medicines for pharmaceutical and biotechnology companies.
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