Manufacturing Sciences & Technology (MS&T) Engineer I

Catalent Pharma Solutions • San Diego, CA

16h • Onsite

About The Position

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.

Requirements

• Bachelor’s degree in Engineering, or Science required; Packaging Engineering or Packaging Sciences preferred.
• Minimum of 1 years of experience with GMP equipment, manufacturing, healthcare, and/or pharmaceutical preferred
• Minimum of 1 years of experience in a customer service or appropriate business-related area
• Demonstrated knowledge of manufacturing equipment and GMP processes, with the ability to manage multiple tasks effectively while maintaining a strong customer service focus.
• Strong communication, teamwork, and professionalism, including excellent written, verbal, and interpersonal skills, a positive attitude, and the ability to meet commitments with a right‑first‑time approach.
• Proficient in Microsoft Office (Word, PowerPoint, Excel, Visio)

Nice To Haves

• Project management experience and skills preferred
• ArtiosCAD experience preferred

Responsibilities

• 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 records, legacy records, master batch records, 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.
• Any other duties which may properly be assigned to this post.
• May be requested to perform any role/level within the CSE team if trained to do so.
• All other duties as assigned.

Benefits

• Competitive salary with bonus potential.
• Generous 401K match and Paid Time Off accrual.
• Medical, dental and vision benefits effective day one of employment.
• 152 hours of PTO + 10 paid holidays.
• Tuition Reimbursement
• WellHub program to promote overall physical wellness.
• Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level