Catalent, Inc.
Contract Development and Manufacturing Organization (CDMO)
ManufacturingSciences&Technology(MS&T)EngineerI
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Manufacturing Sciences & Technology (MS&T) Engineer I at Catalent, Inc.. Skills: technical process support, package and process development, technology transfer, technical documentation, cGMP compliance. coordinate projects ensuring correct technical requirements documentation generated, monitored and assist to ensure successful adherence and completion. Attend and produce minutes and actions for internal client meetings”
What You'll Achieve.
successful adherence and completion of projects; implement and sustain processes
Industry & Context.
root cause analysis
100% on-site (San Diego), standing, walking, sitting, kneeling, push/pulling frequently, significant amount of use of office, lift up to 35lbs, work in temperature-controlled freezers/fridges occasionally
What They're Looking For.
Must Have
Bachelor's degree in Engineering, or Science Packaging Engineering or Packaging Sciences, Minimum of 1 years of experience with GMP equipment, manufacturing, healthcare, and/or pharmaceutical, Minimum of 1 years of experience in a customer service or appropriate business-related area, Demonstrated knowledge of manufacturing equipment and GMP processes, ability to manage multiple tasks effectively while maintaining a customer service focus, communication, teamwork, and professionalism, excellent written, verbal, and interpersonal skills, a positive attitude, ability to meet commitments with a right‑first‑time approach, Proficient in Microsoft Office (Word, PowerPoint, Excel, Visio)
Nice to Have
Project management experience and skills, ArtiosCAD experience
What You'll Do.
coordinate projects ensuring correct technical requirements documentation generated
monitored and assist to ensure successful adherence and completion
Attend and produce minutes and actions for internal client meetings
Support authoring technical reports
product and equipment specifications
protocols and any other technical documents not listed in support of tech transfer and cGMP activities
Assist with departmental training and completion of training documentation
Assist in the preparation and regular review of Standing Operating Procedures relating to your own areas of responsibility
Support Complaint & Deviation investigations and root cause analysis
Stay appraised of development within the healthcare packaging industry
How You'll Work.
Team & Collaboration
partners cross‑functionally with project management, manufacturing, quality, supply chain, labeling, and facilities teams; coordinate projects; Attend and produce minutes and actions for internal client meetings; promote professionalism, communication, and customer service excellence as a Catalent Operations advocate
Communication Scope
excellent written, verbal, and interpersonal skills; communication
Process & Methodology
coordinate projects, manage multiple tasks effectively
Full Job Description
**Manufacturing Sciences and Technology (MS &T) Engineer I** **Position Summary:** * **Work Schedule:** Monday-Friday, 8:00am-4:30pm * 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Our purpose-built San Diego location provides comprehensive clinical supply services including clinical supply management, primary and secondary packaging, complex labeling services, clinical storage, distribution, and clinical returns and destruction, and will also include stability chambers. Located less than a mile from Catalent’s West Coast early-phase oral drug product development center of excellence, customers choosing this convenient Catalent location can now enjoy a fully integrated development, clinical supply manufacturing and distribution solution. The Manufacturing Sciences and Technology (MS&T) team provides technical process support for San Diego Ware operations, leading package and process development and acting as the technology transfer owner for assigned projects. This role supports internal and external technology transfers, packaging component design, and technical documentation in compliance with cGMP and change control requirements. The position partners cross‑functionally with project management, manufacturing, quality, supply chain, labeling, and facilities teams to implement and sustain processes, while promoting continuous improvement, professionalism, strong communication, and customer service excellence as a Catalent Operations advocate. **The Role:** * Under leadership of MS&T, coordinate projects ensuring correct technical requirements documentation generated, monitored and assist to ensure successful adherence and completion. * Attend and produce minutes and actions for internal client meetings to support MS&T team and understand full scope requirements to generate required project requirements documentation. * Support authoring technical reports, source documents, SupplyFlex reco
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