Quality Assurance Associate (Pompano Beach, FL)
CEDENT
Client is seeking an entry-level Quality Assurance / Quality Control Associate to support clinical manufacturing and drug development activities in a GMP-regulated environment. This is a great opportunity for individuals looking to begin their careers in biotech, particularly in quality and regulatory compliance. Key Responsibilities:
- Receive and qualify incoming materials and reagents according to GMP requirements
- Review batch records, laboratory notebooks, and QC testing results for completeness and compliance
- Assist in deviation investigations and document change control processes
- Support the organization and maintenance of the electronic document control system
- Ensure compliance with internal SOPs and applicable cGMP regulations
- Participate in internal audits and prepare documentation for regulatory inspections
- Assist with data verification and archiving of quality-related records
- Contribute to creation and revisions of SOPs, forms, and controlled documents
- Associate’s or Bachelor’s degree in Biomedical Sciences, Life Sciences, or a related field
- Candidates with degrees in Data Management, Health Information Technology, Technical Writing, Supply Chain Management, or Communications who are looking to enter the biotech industry are also encouraged to apply
- Strong attention to detail and organizational skills
- Effective written and verbal communication skills
- Ability to review and interpret technical documents and records
- Self-motivated with the ability to work independently and as part of a team
- Comfortable using digital tools and electronic documentation systems
- Willingness to work in a GMP-regulated laboratory environment
Vacancy posted more than 2 months ago
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