Piper Health Sciences is seeking a QA Document Control Specialist to join a clinical-stage biotech company located in Elkridge, MD . The QA Document Control Specialist will be responsible for filing and archiving GMP documents. Responsibilities of the QA Document Control Specialist include:
- Create and update documents by writing, formatting, and editing
- Utilize electronic document systems for all documentation
- Initiate new SOPs and revise existing SOPs
- Collaborate with various teams to facilitate document review, approval, and distribution processes
- Follow SOPs (Standard Operating Procedure) to support the document approval process
Qualifications for the QA Document Control Specialist include:
- 2-5 years of experience in a GMP environment
- Previous document control experience, handling batch records, and performing batch record reviews
- Experience using electronic document control systems
- Associate degree or Bachelor's degree
Compensation for the QA Document Control Specialist include:
- Rate Range: $25 - $35 Per Hour depending on experience
- Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401k
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