Catalent, Inc.

Contract Development and Manufacturing Organization (CDMO)

ManufacturingSciences&Technology(MS&T)EngineerI

$90–100k San Diego, California, United States FULL TIME
The Brief

“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.

Contract Development and Manufacturing Organization (CDMO)
Problems you'll solve

root cause analysis

Eligibility Requirements

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

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