Biopharma SOPs & GDE Technical Writer
Listed on 2026-11-05
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Pinnaql seeks a Technical Writer to develop and revise SOPs and Global Documents Engineering (GDE) documentation for a biopharmaceutical manufacturing environment. You will ensure clarity and compliance across engineering systems, equipment, and manufacturing support processes.
Collaborating with Engineering, Manufacturing, Validation, and Quality, you will translate technical requirements into precise documents, manage revisions, and drive approval workflows within the EDMS to support GMP
This role, Biopharma SOPs & GDE Technical Writer at Veg Group, could be your next move.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Biopharma SOPs & GDE Technical Writer role in the description above.
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