Remote GMP Quality Mgr

Job Description

Job Description

Remote GMP Quality Mgr needs 8+ years of experience required, with relevant experience in biotech or pharmaceutical industry with most experience in a Quality role.

Advanced knowledge of GMP manufacturing and/or market release of pharmaceutical dosage forms and/or combination products.

Experience with managing external CMOs, contract laboratories, and third-party logistics suppliers.

Must have experience in reviewing and approving master and executed batch records and performing final disposition of drug substances and products.

Experience managing quality events (investigations, CAPA and change control), and working knowledge of formal risk management tools and assessments. The individual must demonstrate the ability to evaluate and assess technically complex quality events, as well as the ability to document these events with excellent technical writing skills.

Experience in evolving GMP related quality systems, policies, and procedures to ensure compliance with evolving standards as well as improving the efficiency of related workflows.

Strong ability to analyze complex issues to develop relevant and realistic plans, programs, and recommendations.

Excellent verbal and written communication skills, including ability to interact effectively with senior management, partners, and project core team members.

Self-motivated, flexible, and able to prioritize work and handle multiple assignments in a fast-paced environment, while maintaining a high level of quality and compliance.

Bachelor's degree in a scientific discipline (e.g., biology, chemistry, engineering, pharmacy) or relevant field of study.

Duties:

Be the QA representative on cross-functional project teams. Responsible for communicating with the Quality and Production departments at domestic and international contract manufacturing organizations, and within SMPA's Quality, Supply Chain, CMC, and Commercial Manufacturing departments.

Conducts product release activities for clinical and commercial drug substances and drug products; including review and approval of Master Batch Records, Executed Batch Records, release and stability testing documentation, and batch disposition. These activities must be conducted in a timely manner to ensure continued product supply while ensuring Quality and Safety of the product.