Associate Director of Manufacturing
Listed on 2026-02-01
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Healthcare
Healthcare Management
Associate Director of Manufacturing role at Medivant Healthcare
2 days ago. Be among the first 25 applicants.
Base pay range$/yr – $/yr
About Medivant HealthcareMedivant Healthcare is a U.S.
-based pharmaceutical manufacturer specializing in sterile injectable generics for hospitals, clinics, and healthcare providers nationwide. Our FDA-registered facilities in Chandler and Deer Valley, Arizona, are dedicated to ensuring consistent product quality, regulatory compliance, and affordable medication access.
The Associate Director of Manufacturing provides strategic and operational leadership for Medivant’s manufacturing operations within a cGMP-regulated environment. This role partners closely with senior leadership to drive operational excellence, ensure regulatory compliance, and support business growth through scalable, efficient, and high‑quality manufacturing processes.
Key Responsibilities- Provide strategic and operational leadership for manufacturing operations across shifts and product lines.
- Oversee production planning, execution, and performance to meet safety, quality, delivery, and cost objectives.
- Ensure compliance with cGMP, FDA, and applicable regulatory requirements.
- Lead, mentor, and develop Manufacturing Managers and Supervisors, fostering accountability and continuous improvement.
- Drive process optimization, capacity expansion, and cost‑efficiency initiatives.
- Collaborate cross‑functionally with Quality, Engineering, Supply Chain, Validation, and Regulatory Affairs.
- Support regulatory inspections, customer audits, and internal compliance assessments.
- Review and approve deviations, CAPAs, change controls, and batch documentation in partnership with QA.
- Contribute to long‑term manufacturing strategy, capital planning, and operational scalability.
- Bachelor’s degree in pharmacy, Engineering, Science, or related field.
- 12–15+ years of experience in pharmaceutical or regulated manufacturing environments.
- Minimum 5–7 years of progressive leadership experience managing managers and large teams.
- Strong expertise in cGMP manufacturing, operational excellence, and regulatory compliance.
- Master’s degree in a related discipline.
- Proven ability to lead complex operations, manage change, and influence senior stakeholders.
- Director
- Full‑time
- Management and Manufacturing
- Industries:
Pharmaceutical Manufacturing
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