Packaging Process Engineer I

Packaging Process Engineer I Position Summary Work Schedule:

Monday to Friday during regular business hours 100% based on-site in Greenville, NC Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. The Packaging Process Engineer I oversees the development, coordination, and continuous improvement of packaging solutions across production operations. Serving as a technical bridge between internal teams, clients, and vendors, it drives requirement gathering, packaging design, and implementation on production equipment. The Role Lead the translation of customer and project requirements into robust, compliant packaging solutions by partnering with clients, internal teams, and vendors; provide technical guidance throughout project scoping, packaging design, and implementation Drive the development, optimization, and continuous improvement of primary, secondary, and tertiary packaging components, including blister formats, container/closure systems, labeling, and cartons—ensuring fit for purpose designs that meet regulatory and product needs Support efficient packaging operations by assisting with equipment setup, qualification, troubleshooting, and serialization activities, identifying root causes of issues, and implementing corrective actions to enhance equipment reliability and line performance Author, maintain, and execute GMP‑compliant engineering documentation, batch record inputs, work instructions, and quality system records while utilizing electronic systems (e.g., TrackWise, EDMS, ComplianceWire) to support investigations, change control, deviations, CAPAs, and training Collaborate cross functionally with Production, Quality Assurance, Validation, Supply Chain, and Facilities to ensure alignment on packaging requirements, operational readiness, and continuous improvement of packaging processes and workflows Manage vendor interactions—including component design, technical evaluations, pricing discussions, and FAT/SAT activities—to ensure timely, cost-effective, and high-quality solutions Support thorough and compliant investigations through structured problem solving and root cause analysis, driving improvements that enhance product quality and packaging integrity Monitor industry trends, materials, and technologies to identify opportunities for innovation, efficiency gains, and standardization across packaging engineering activities Contribute to project execution by tracking milestones, documentation, and deliverables while helping maintain internal tools such as blister format libraries and equipment documentation Other duties assigned The Candidate Master's degree in Engineering discipline (e.g. Packaging Mechanical, Chemist, Industrial, or related) OR Bachelor's degree in Engineering discipline with 2+ years of experience in the pharmaceutical industry or regulated manufacturing industry required Degree in Packaging Sciences strongly preferred Foundational understanding of pharmaceutical packaging operations, including serialization processes Working knowledge of cGMPs, applicable industry standards, and regulatory guidelines Basic understanding of federal and local health and safety regulations relevant to manufacturing and packaging environments Ability to lift objects weighing 40 pounds without assistance Ability to use hands for repetitive simple grasping and fine motor manipulation Ability to bend, squat, reach, and push as required by job duties Ability to stand and remain on feet for extended periods of time Ability to work safely with hazardous chemicals and active chemical ingredients This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent. Why You Should Work At Catalent Spearhead exciting and innovative projects Fast-paced, dynamic environment High visibility to members at all levels of the organization 152 hours of 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. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. 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 DisabilityAccommodations@catalent.com. 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. Notice to

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Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.