GMP QA Specialist – Clinical Supply & Documentation

Biotech Networks, LLC; Rahway (NJ); On-site; USD 90,000 - 120,000; Full time

Job summary

Biotech Networks, LLC is seeking a Specialist, Quality Assurance to review and approve documentation supporting GMP clinical supply drug product manufacture, testing, release and maintenance of our clinical supply programs. The role independently conducts review and routine audits of batch documentation, data, procedures and equipment to ensure compliance with GMP standards and internal SOPs.

The position emphasizes accuracy, timeliness, and meticulous adherence to regulatory requirements in a

Job description

Biotech Networks, LLC is seeking a Specialist, Quality Assurance to review and approve documentation supporting GMP clinical supply drug product manufacture, testing, release and maintenance of our clinical supply programs. The role independently conducts review and routine audits of batch documentation, data, procedures and equipment to ensure compliance with GMP standards and internal SOPs.

The position emphasizes accuracy, timeliness, and meticulous adherence to regulatory requirements in a