Vice President, MSAT
PCI Pharma Services
Summary
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Job description
Essential Duties and Responsibilities
- Optimize the deployment of technical resources, manufacturing assets, and support functions across the network to maximize capacity utilization, process robustness, operational efficiency, and future growth capabilities.
- Provide strategic leadership and technical oversight for complex investigations, change controls, risk assessments, and gap analyses across all manufacturing modalities, ensuring consistent execution and regulatory compliance throughout the organization.
- Establish and govern standards for technical documentation, change management, technology transfers, and compliance-related activities supporting critical MSAT and NPI initiatives.
- Lead technical and business assessments of new client opportunities to ensure strategic fit, technical feasibility, regulatory compliance, capacity alignment, and long-term profitability across the network.
- Serve as the technical escalation point for major client engagements, regulatory inspections, and customer audits, providing expert guidance on complex manufacturing and process challenges.
- Develop and sustain an integrated innovation and technology roadmap linking MSAT, NPI, Engineering, and Manufacturing to accelerate commercialization, improve process capability, and advance future manufacturing technologies.
- Lead the cross-functional client technical intake and governance process, aligning commercial, technical, quality, and operational stakeholders to support successful project selection and execution.
- Drive enterprise-wide change management initiatives, ensuring alignment and adoption across MSAT, NPI, Manufacturing, Engineering, Quality Assurance, Quality Control, and Supply Chain functions.
- Act as the executive technical sponsor for strategic technology transfers, process performance improvements, lifecycle management initiatives, and network harmonization efforts.
- Serve as a senior technical consultant and subject matter expert on complex operational, process, and client-related challenges across the organization.
- Foster a culture of collaboration, technical excellence, innovation, and client focus while maintaining the highest standards of professionalism and compliance.
- Represent the organization during client interactions, governance forums, technical reviews, and executive leadership discussions involving product transfers, manufacturing readiness, compliance strategy, and process improvement initiatives.
- Develop and maintain strong collaborative relationships with internal stakeholders and external partners to ensure successful execution of technical and business objectives.
- Ensure compliance with all applicable PCI policies, cGMP regulations, quality standards, and Environmental Health and Safety (EHS) requirements.
Qualifications
- Bachelor's degree in Life Sciences or equivalent experience required.
- Minimum of fifteen (15) years of relevant experience in cGMP manufacturing or equivalent.
- Proven experience leading innovation, managerial experience with extensive industry knowledge and an eye towards future technologies.
- Strategic thinking, adaptive thinking, and strong critical mindset.
- Strong business acumen and presentation skills.
- Excellent interpersonal, leadership, and communication skills.
- Impact & influence top leaders & external clients and regulators.
- Emphasis on aseptic processing and compliance required.
- Advanced-level verbal communication skills.
- Directs and provides expert knowledge of MSAT strategies, standards, and processes to support technology transfer, new product introduction (NPI), process.
- Identifies, recruits, and retains top-notch talent.
- Champions PCI Pharma Services culture and empowers employees to take responsibility for their jobs and goals.
- Coaches, mentors, engage and develop the team, including overseeing new employee onboarding and providing career development planning and learning opportunities.
- Sets performance standards and encourages employee engagement and results through delegation, continuous feedback, goal setting, and performance management.
- Maintains transparent communication.
- Provides oversight and direction to the employees in accordance with PCI Pharma Services policies and procedures.
Work Environment
Effective verbal and written communication with both internal and external contacts is critical to success. Interacts with members of the leadership team and may present to the Board of Directors as required. Must be able to interact effectively with internal and external clients. Oversees a wide array of subordinate managers, supervisors, and operations employees. Travel < 15% of the time.
Requirements
- Bachelor's degree in Life Sciences or equivalent experience required
- Minimum of fifteen (15) years of relevant experience in cGMP manufacturing or equivalent
- Proven experience leading innovation
- Managerial experience with extensive industry knowledge
- Strategic thinking, adaptive thinking, and strong critical mindset
- Strong business acumen and presentation skills
- Excellent interpersonal, leadership, and communication skills
- Impact & influence top leaders & external clients and regulators
- Emphasis on aseptic processing and compliance required
- Advanced-level verbal communication skills
- Expert knowledge of MSAT strategies, standards, and processes to support technology transfer and NPI
Benefits
- Paid Time Off
- Health Insurance
- Dental Insurance
- Vision Insurance
- Flexible Spending Account
- 401(k)
- Annual Performance Bonus Eligibility
Company overview
PCI Pharma Services is a global contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical supply chain solutions to pharmaceutical and biopharmaceutical companies worldwide. Founded in 1991 and headquartered in Philadelphia, Pennsylvania, the company has established itself as a trusted partner in the healthcare industry, offering integrated services that span the entire drug development lifecycle. PCI specializes in drug development support, clinical trial supply management, contract drug manufacturing, sterile and non-sterile drug product packaging, and global pharmaceutical logistics. With a global footprint encompassing 30 GMP-compliant facilities across multiple continents, the company serves as a strategic partner that follows the molecule from early development through commercial launch. PCI's expertise enables clients to accelerate time-to-market while ensuring regulatory compliance and quality standards. The company's comprehensive service portfolio includes analytical services, formulation development, commercial manufacturing, packaging, supply chain management, and distribution, making it a one-stop solution for pharmaceutical companies seeking to outsource their development and manufacturing needs.