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Manager, Manufacturing Science & Technology

Position Summary:

• Work Schedule: Monday- Friday, 8:00am to 5:00pm
• 100% on-site

The Morrisville (MSV) facility is Catalent’s center of excellence for nasal product development and manufacturing, providing end‑to‑end services from early formulation through clinical and commercial production. The site offers comprehensive nasal development capabilities, including analytical support, device selection, spray characterization, and both clinical and commercial scale for unit‑dose, bi‑dose, and multidose nasal products. The Morrisville site also provides development services for dry powder (DPI) and liquid pulmonary products including formulation development and optimization, method services and analytical testing.   

This role provides technical support for process performance, troubleshooting, technology transfer, and continuous improvement activities. The Manager collaborates closely with Manufacturing, Quality, and Development to maintain product quality, ensure compliance, and drive operational efficiency.

The Role:

• Plan and execute defined experimental studies, process evaluations, and equipment qualification activities, including review technical reports, protocols, and data packages to ensure accuracy and completeness
• Maintain process, analytical, and raw material knowledge needed to support ongoing production and investigations
• Provide technical support for formulation, compounding, fill/finish, assembly, packaging, and labeling operations to ensure compliant and reliable manufacturing
• Assist with technology transfer activities for clinical and commercial manufacturing, including coordination with internal and external partners to ensure production schedules maintained and processes are run reliably and compliantly.
• Monitor critical quality attributes (CQAs) and critical process parameters (CPPs) to detect trends and recommend corrective actions
• Lead investigations to determine root cause and support CAPA development using structured problem‑solving tools (e.g., FMEA, Fishbone, DOE).
• Other duties as assigned 

The Candidate:

• Requires Master’s Degree in Biochemistry, Chemical Engineering, Bioengineering, or related technical field with 5+ years of GMP pharmaceutical manufacturing experience OR
• Bachelor’s Degree in Biochemistry, Chemical Engineering, Bioengineering, or related technical field 7+ years of GMP pharmaceutical manufacturing experience
• Experience supporting formulation or non‑sterile fill/finish operations in a GMP environment is required
• Familiarity with cGMP regulations for non‑sterile liquid products and basic validation/qualification principles is required
• Working knowledge of 21 CFR Part 4 and 21 CFR Part 820 expectations for nasal spray combination products is preferred
• Experience with DOE/statistical tools and analytical method development is preferred

Why you should join Catalent:

• Defined career path and annual performance review and feedback process 
• Diverse, inclusive culture 
• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 
• 152 hours of PTO + 8 paid holidays
• Generous 401K match 
• Medical, dental and vision benefits
• Tuition Reimbursement- Let us help you finish your degree or start a new degree!

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 Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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