Regulated Documentation Specialist

3 weeks ago


Raleigh, North Carolina, United States Technical Source Full time
As a Documentation Specialist at Technical Source, you will be responsible for managing and organizing critical documentation in a pharmaceutical manufacturing environment. This role requires strong organizational skills, attention to detail, and familiarity with regulated manufacturing processes.

The ideal candidate will have experience in documentation or administrative roles within the pharmaceutical or biotech industry. You will work closely with validation and process engineering teams to ensure timely and accurate documentation.

Your responsibilities will include creating, reviewing, and maintaining accurate documentation related to validation protocols, reports, process changes, and SOPs. You must ensure that all documents meet GMP, FDA, and other regulatory standards, maintaining audit readiness at all times.

The salary range for this position is $70,000 - $90,000 per year, depending on experience.

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