An established industry player is seeking a detail-oriented QA Associate Specialist to enhance their Document Control operations. This role is vital in supporting the cGMP Document Control processes, including document approvals and change control. The ideal candidate will possess strong communication skills and a proactive mindset, ensuring compliance with regulatory standards while working collaboratively across departments. Join a dynamic team where your contributions will directly impact quality assurance and operational excellence in a fast-paced environment. If you're passionate about quality and continuous improvement, this opportunity is perfect for you.
Qualifications
1+ year of document control experience in a cGMP/FDA regulated environment.
Strong communication and customer service skills required.
Responsibilities
Manage electronic document system and document change requests.
Support audits and regulatory inspections as needed.
Generate reports for Quality Council metric reporting.
Skills
Document Control
Technical troubleshooting
Communication
Cross-functional collaboration
Self-motivated
Education
Bachelor's degree or equivalent
Tools
MS Office
Document Management System
Quality Management System
Adobe
Visio
Excel
Job description
An established industry player is seeking a detail-oriented QA Associate Specialist to enhance their Document Control operations. This role is vital in supporting the cGMP Document Control processes, including document approvals and change control. The ideal candidate will possess strong communication skills and a proactive mindset, ensuring compliance with regulatory standards while working collaboratively across departments. Join a dynamic team where your contributions will directly impact quality assurance and operational excellence in a fast-paced environment. If you're passionate about quality and continuous improvement, this opportunity is perfect for you.