Manager Production Services
Parexel
Manager Production Services
Parexel
End-to-end clinical trials and regulatory consulting
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
About Parexel
Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart®.
About the Role
We are seeking a Manager, Production Services (Clinical Trial Supply Chain / Clinical Logistics Operations Manager) to join our Clinical Trial Supplies & Logistics (CTS&L) team in a remote U.S./Pennsylvania-based capacity, with preference given to candidates located within reasonable proximity to our Quakertown, Pennsylvania depot.
This newly created leadership role will help shape the future structure of a global Production Services team responsible for clinical trial supply packaging, labeling, manufacturing support, production planning, and batch documentation activities. The Manager, Production Services will provide operational leadership, technical guidance, and day-to-day oversight across critical clinical supply chain functions while ensuring compliance with Good Manufacturing Practices (GMP) requirements, sponsor expectations, quality standards, and delivery timelines.
You will partner with cross-functional teams across North America, Europe, Asia, and Latin America to support the successful delivery of clinical trial materials that directly impact patients around the world. This position offers a unique opportunity to step into a visible leadership role, influence team strategy, and drive operational excellence within a growing global organization.
Key Responsibilities
Lead, mentor, and develop Production Services team members while fostering a collaborative, high-performance culture.
Oversee clinical trial supply production workflows, ensuring projects remain on schedule and deliverables are achieved.
Monitor operational progress, manage priorities, and provide escalation support for complex supply chain challenges.
Support packaging, labeling, manufacturing support, batch documentation, and production planning activities.
Ensure compliance with Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), regulatory requirements, and departmental procedures.
Drive problem solving and mitigation planning to address project risks and timeline challenges.
Support supplier compliance, quality metrics, training compliance, audits, inspections, CAPA activities, and continuous improvement initiatives.
Collaborate with cross-functional clinical supply chain stakeholders to ensure successful project execution and customer satisfaction.
Contribute to operational excellence, process improvement initiatives, and lean management practices.
Support business growth through participation in internal initiatives, client-facing activities, and strategic operational planning.
Candidate Profile
You'll thrive in this role if you bring:
Strong leadership, problem-solving, and operational decision-making skills.
Expertise in clinical trial supply chain operations and GMP-regulated environments.
Experience supporting packaging, labeling, production planning, and clinical supply activities.
The ability to influence teams, prioritize competing demands, and navigate operational challenges.
Strong communication and collaboration skills with global cross-functional teams.
A customer-focused mindset with a passion for delivering solutions that ultimately support patients.
Required Qualifications
Bachelor's degree in Life Sciences, Pharmaceutical Sciences, Logistics, Engineering, or a related discipline, or equivalent experience.
Approximately 6 to 10+ years of experience in clinical trial supply chain, pharmaceutical production, clinical logistics, or a related regulated environment.
Strong knowledge of Good Manufacturing Practices (GMP) requirements and clinical supply chain operations.
Experience with production planning, packaging design, labeling operations, and supply chain execution.
Ability to identify risks, resolve operational issues, and implement mitigation strategies.
Strong project management, organizational, and stakeholder management skills.
Fluent English communication skills.
Preferred Qualifications
Experience within a Contract Manufacturing Organization (CMO) supporting clinical trial supplies.
Previous people leadership or team management experience.
Pharmaceutical Sciences educational background or equivalent pharmaceutical industry expertise.
Experience leading global or geographically dispersed teams.
Financial, budgeting, profitability, KPI, and forecasting experience.
Benefits and Compensation
Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings Accounts
Work/Life Balance
401(k) with Company Match
Pet Insurance
For a complete list of benefits, please visit www.parexel.com/us-benefits.
We offer a comprehensive benefits package to eligible employees, which includes paid time off, a 401(k) match, life insurance, health insurance, and additional benefit offerings in accordance with the terms of our applicable plans.
If this job doesn't sound like the next step in your career, but perhaps you know someone who would be a perfect fit, send them the link to apply!
We believe in flexibility, growth, and creating space for people to do their best work. Join us and help deliver clinical trial supplies that accelerate the development of life-changing therapies for patients worldwide.
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.
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