Senior GMP Technical Writer - QC Investigations Lead
Johnson & Johnson Co.
Johnson & Johnson seeks a Technical Writer for the NJ Stability Lab Operations to lead GMP documentation and investigations, ensuring compliance with cGMP and regulatory guidelines. You will drive authoring of SOPs, validation protocols and reports from conception to utilization. You will proofread, review data, and participate in gap assessments to maintain current standards while supporting audit readiness and continuous improvement in laboratory documentation. #J-18808-Ljbffr Johnson & Johnson Co.
Vacancy posted 4 days ago
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