Director of Operations (Pharma Packaging & Manufacturing)
Audubon, Pennsylvania
Job Id:
162289
Job Category:
Life Sciences
Job Location:
Audubon, Pennsylvania
Security Clearance:
None
Business Unit:
Piper Companies
Division:
Piper Clinical Solutions
Position Owner:
Karen Pallone
Piper Companies is seeking a Director of Operations (Pharma Packaging & Manufacturing) for an opportunity in Audubon, Pennsylvania (PA), to join an award-winning drug development solutions provider at the forefront of the pharmaceutical industry.
Location: Audubon, PA
Compensation: $200,000-$220,000, bonus eligibility
Seeking a Director of Operations to lead site-wide operational functions at a key U.S. facility. This individual will oversee packaging, maintenance, logistics, and warehousing operations, ensuring delivery against production goals while maintaining strict cGMP compliance, operational excellence, and continuous improvement.
Responsibilities
- Ensure safe, compliant, and efficient execution of production schedules in alignment with business objectives
- Serve as a key member of the site leadership team, contributing to both site-level and global initiatives
- Drive a culture of continuous improvement (OEE, operational excellence, Lean principles)
- Lead and develop high-performing teams, setting clear expectations around performance, compliance, and accountability
- Partner with global counterparts to ensure alignment of processes, systems, and best practices
- Oversee operational projects, including process improvements, ERP implementations, and site initiatives
- Build strong client relationships by delivering consistent, high-quality operational performance
- Ensure readiness and interaction with regulatory agencies (FDA, etc.)
Qualifications
- Bachelor’s degree in Life Sciences, Engineering, or related field
- 10+ years of leadership experience in a pharmaceutical or regulated production environment
- Master’s degree in a related discipline
- 5+ years in a senior operations leadership role within pharma manufacturing
- 10+ years of experience in manufacturing/production operations
- Strong background in cGMP environments with proven compliance track record
- Demonstrated success driving continuous improvement / OEE initiatives
- Experience leading change management efforts to improve efficiency and performance
- Ability to operate in a fast-paced environment and manage competing priorities
- Experience interfacing with regulatory agencies (FDA or equivalent)
This job opens for applications on 3/16/2026. Applications for this job will be accepted for at least 30 days from the posting date.
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