QA Documentation Specialist — GMP & Compliance

Lupin is looking for a Quality Assurance Specialist to manage document lifecycle at their Coral Springs site. Responsibilities include ensuring compliance with regulations, issuance of GMP documents, and collaboration across departments to maintain quality standards.
This role requires 1-3 years of experience in an FDA environment and a degree in a related field. Strong communication skills and an understanding of cGMP regulations are essential for success in this position.

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