Quick overview
Job description
We are seeking an experienced Quality Assurance professional to support clinical packaging and labeling operations within a GMP-regulated pharmaceutical environment. The ideal candidate will oversee quality activities related to clinical trial materials, ensuring compliance with GMP requirements and applicable quality standards.
Required Qualifications:
Bachelor's degree in a scientific discipline, Pharmaceutical Sciences, or a related field.
7+ years of experience in Pharmaceutical Quality Assurance, Quality Operations, or GMP-regulated environments.
Hands-on experience with clinical packaging and labeling operations.
Strong knowledge of GMP requirements, Investigational Medicinal Products (IMPs), and clinical supply processes.
Experience reviewing batch records, managing deviations, CAPAs, change controls, and quality documentation.
Experience working with Contract Manufacturing Organizations (CMOs) and external pharmaceutical vendors.
Strong technical writing, communication, organizational, and risk assessment skills.
Preferred Qualifications:
Experience supporting early-phase clinical development programs.
Experience with vendor quality oversight, audits, and quality agreements.
Familiarity with electronic Quality Management Systems (eQMS) and document management platforms.
Ability to manage multiple priorities in a fast-paced clinical supply environment.
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