Associate Director of Manufacturing

Medivant Healthcare

Chandler (AZ)

On-site

USD 110,000 - 120,000

Full time

14 days+

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Job summary

A pharmaceutical manufacturer based in Chandler, AZ is seeking an Associate Director of Manufacturing to provide strategic and operational leadership. The ideal candidate will have at least 12 years of experience in regulated manufacturing and strong expertise in cGMP and operational excellence. Responsibilities include overseeing production, ensuring compliance with regulations, and mentoring management staff. This full-time position offers competitive pay and the opportunity to influence manufacturing strategy.

Qualifications

12–15+ years in pharmaceutical or regulated manufacturing environments.
5–7 years managing managers and large teams.
Strong expertise in cGMP, operational excellence, and regulatory compliance.

Responsibilities

Provide strategic and operational leadership for manufacturing operations.
Oversee production planning, execution, and performance.
Ensure compliance with cGMP, FDA, and regulatory requirements.
Lead, mentor, and develop Manufacturing Managers and Supervisors.
Drive process optimization and cost‑efficiency initiatives.

Skills

cGMP manufacturing

Operational excellence

Regulatory compliance

Leadership

Education

Bachelor's degree in pharmacy, Engineering, Science

Master's degree in a related discipline

Job description

Associate Director of Manufacturing role at Medivant Healthcare

2 days ago. Be among the first 25 applicants.

Base pay range

$110,000.00/yr – $120,000.00/yr

About Medivant Healthcare

Medivant 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.

Position Summary

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.

Required Qualifications

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.

Preferred Qualifications