Manager Manufacturing Engineering QA

Manager, Manufacturing Engineering Quality Assurance

Base pay range : $122,850.00 / yr - $150,150.00 / yr

Responsibilities

• Responsible for GMP facility utilities design review and qualification.
• Primary driver and overseer for manufacturing deviation investigations and product disposition decisions regarding environmental impact on product quality.
• Provide quality oversight to GMP facility maintenance and calibration programs.
• Drive GMP facility environmental monitoring and qualification.
• Manage all GMP facility manufacturing monitoring and alarm systems qualification.
• Oversee all GMP equipment qualification and equipment deviation investigations and resulting outcomes with regards to specific batch of radiopharmaceutical product, as well as possible impact on all product batch manufacture, past and future.
• Oversee quality of all GMP process validation.
• Non‑conformance of GMP facility temperature‑controlled areas qualification and drive investigators and approvals on such system investigation.
• Ensure manufacturing site compliance with current U.S. and EU cGMP regulations and industry standards as defined by Aktis Quality System.
• Oversee GMP facility change control events, assuring proper consideration of potential impact to product quality and assuring process is executed per Aktis Change Control system, giving final approval to product change.
• Provide quality engineering oversight of modification and construction review and approvals for Aktis GMP manufacturing space.
• Provide leadership to staff by directing, mentoring, coaching and developing them towards professional growth, enhanced job performance and career satisfaction.
• Provide input for continuous improvement of company’s quality systems.
• Identify quality issues / discrepancies, and effectively and proactively resolve them in a diplomatic, flexible and constructive manner.
• Oversee all quality aspects of technology transfer of product manufacturing and control systems to external third‑party contract or internal manufacturing site.
• Manage GMP responsibilities for all in‑house GMP site engineering.
• Build collaborative working relationships and effective communications with all stakeholders in all manufacturing operations, analytical testing, quality systems, regulatory, etc., at all levels.
• Establish, educate, and enforce standard operating procedures required under GMP.
• Lead investigations using root cause analysis techniques, ensuring effective corrective actions and preventive actions.
• Identify performance or compliance gaps and implement or propose solutions.
• Maintain a state of readiness for and participate in audits and inspections of Aktis’ in‑house GMP manufacturing space and associated utilities.
• Manage complexities within a product development environment to plan, organize, execute, monitor staff assignments and all activities necessary to achieve continuous clinical and commercial supply.

Knowledge, Skills, and Abilities

Preferred Experience and Skills

Education and Experience

BS / BA degree in a scientific or allied health field with 4+ years of relevant work experience, or relevant comparable background in biologics or drug product manufacturing. Radiopharmaceutical background / experience a plus.

The position reports directly to the Vice President of Quality Assurance.

Aktis Oncology is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, disability, national origin, veteran status, or any other basis covered by appropriate law. Aktis Oncology is committed to promoting and maintaining a work environment in which all applicants, employees, and other individuals are treated with dignity and respect free from unlawful harassment, discrimination, or retaliation.

Seniority Level

Mid‑Senior level

Employment Type

Full‑time

Job Function

Quality Assurance

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