Project Engineer, Process Engineer
Listed on 2026-01-14
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Engineering
Process Engineer, Quality Engineering, Manufacturing Engineer, Operations Engineer
Position Summary
Catalent’s Winchester location is the flagship U.S. manufacturing site for large‑scale oral dose forms, offering integrated analytical and development services. With 28 years of expertise in product development, technology transfer, and commercial manufacturing, and roots in industry‑leading Glatt technology, the facility supports breakthrough therapies.
The Project Engineer is a member of the Capital Projects Team within the Continuous Improvement, Technology, and Engineering Department. The role drives the site and facility improvement agenda and supports the Site Capital Plan.
Role- Ensures compliance to scope, cost and schedule.
- Drives continuity and development of standards in Project Engineering to ensure smooth and effective communication flow between internal resources and customers, operational efficiency, and equipment and personnel safety.
- Develops and synchronizes site functions transition through four distinct construction phases (design, build, qualify, validate).
- Maintains project compliance in accordance with the site quality management system.
- Prioritizes and guides engineering resources in the design of facility and equipment within budget.
- Guides the specification and selection of manufacturing/utility equipment to support site facility/process needs; works with operations, validation, process development and quality functions to provide support for the design, installation, start‑up, validation and operation of facility and/or process equipment.
- Effectively manages contractors and ensures adherence to safe work practices and guidelines.
- While not executing projects, supports site operations and process engineers.
- Other duties as assigned.
- Bachelor’s Degree in Engineering (required). Master’s Degree in Engineering or Business is a plus.
- 3+ years of Engineering Project Management experience preferred.
- Prior experience with pharmaceutical facility construction, equipment/facility qualification & validation preferred.
- Experience managing external vendors and project budgeting.
- Hands‑on experience with a combination of process, controls, and equipment engineering is required; change control and validation experience is critical.
- Six Sigma / Lean Manufacturing / Professional Project Management skills preferred.
- Ability to sit for extended periods; vision requirements include reading written documents and using a computer monitor.
- Several Employee Resource Groups focusing on D&I.
- Tuition Reimbursement – Let us help you finish your degree or earn a new one!
- Generous 401(k) match.
- 152 hours accrued PTO + 8 paid holidays.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life‑saving and life‑enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to Disabili This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
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Thank you.
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