Cedent Consulting
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
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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
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