Quality Assurance Associate Position Available In Broward, Florida
Tallo's Job Summary: Client CEDENT in Pompano Beach, FL is hiring an entry-level Quality Assurance/Quality Control Associate with a salary range of $38K - $45.3K a year. Responsibilities include reviewing batch records, assisting in deviation investigations, and ensuring compliance with internal SOPs and cGMP regulations. Qualifications include a degree in Biomedical Sciences or related fields, strong attention to detail, and effective communication skills.
Job Description
Quality Assurance Associate
CEDENT – 5.0
Pompano Beach, FL Job Details Estimated:
$38K – $45.3K a year 23 hours ago Qualifications GMP Bachelor’s degree Organizational skills Manufacturing Associate’s degree Communication skills Entry level Full Job Description 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
Qualifications:
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
