Quality Control Document Specialist

glenmarkpharma

6 days ago

Monroe, NC

Onsite

Full Time

Junior

0 applicants

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About this role

A Quality Control Document Specialist manages documentation for quality control functions, creates and revises specifications and procedures, and ensures compliance with regulations. The role involves collaboration with cross-functional teams and regulatory surveillance programs.

Skills

Qualifications

Bachelor of Science (Chemistry, Biology, Pharmaceutical Sciences, or equivalent)

About glenmarkpharma

glenmarkpharma-us.com

Glenmark Pharmaceuticals U.S. is the U.S. arm of Glenmark Pharmaceuticals, a global biopharmaceutical company focused on discovering and delivering advanced therapies and value-driven generics. It pursues science-led research and development and the commercialisation of medicines across multiple therapeutic areas, supported by a worldwide manufacturing and supply network. The company emphasizes innovative science, rigorous quality and regulatory excellence, and strategic partnerships to bring medicines to patients in North America and beyond. With a patient-centric approach and global reach, Glenmark aims to improve access to high-quality therapies in a changing healthcare landscape.