Quality Assurance Associate

Quality Assurance / Quality Control AssociateClient 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 requirementsReview batch records, laboratory notebooks, and QC testing results for completeness and complianceAssist in deviation investigations and document change control processesSupport the organization and maintenance of the electronic document control systemEnsure compliance with internal SOPs and applicable cGMP regulationsParticipate in internal audits and prepare documentation for regulatory inspectionsAssist with data verification and archiving of quality-related recordsContribute to creation and revisions of SOPs, forms, and controlled documentsQualifications:Associate's or Bachelor's degree in Biomedical Sciences, Life Sciences, or a related fieldCandidates 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 applyStrong attention to detail and organizational skillsEffective written and verbal communication skillsAbility to review and interpret technical documents and recordsSelf-motivated with the ability to work independently and as part of a teamComfortable using digital tools and electronic documentation systemsWillingness to work in a GMP-regulated laboratory environment