Catalent Pharma Solutions Inc

Reliability Engineer

Catalent Pharma Solutions Inc$80K — $110K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Electrical/Mechanical Engineering or related field (3-5 years experience) OR High School Diploma/GED with 5-10 years relevant equipment maintenance experience.
  • Proficient in MS Office (Word, Excel, Visio, Outlook).
  • Experience with Good Manufacturing Principles (GMP).
  • Strong verbal and written communication skills.
  • Ability to lift, push, or pull 0-40 pounds as required.

Responsibilities

  • Collaborate with Process Development on equipment specifications and sourcing for new product introductions.
  • Analyze operational data to identify cost-reduction opportunities and implement process improvements.
  • Manage project plans for equipment implementation, building relationships with stakeholders.
  • Ensure equipment compliance within preventative maintenance programs and oversee reliability initiatives.
  • Design and implement improvements to quality, cost, productivity, and cycle times.
  • Perform additional duties as assigned.

Benefits

  • Defined career path with performance reviews.
  • Inclusive company culture promoting diversity.
  • Opportunities for career advancement in a growing team.
  • 152 hours of PTO plus 8 paid holidays.
  • Generous 401K match plan.
  • Comprehensive medical, dental, and vision benefits.
  • Tuition reimbursement support for education advancement.
Full Job Description

Reliability Engineer

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.   

The Reliability Engineer will support all major capital projects involving the onboarding of equipment. In addition, the equipment engineer will be responsible for ensuring all applicable equipment is placed in a compliant preventative maintenance system.

The Role:

  • Partner with Process Development on new product introductions, focusing on equipment specification, design, and sourcing
  • Develop deep knowledge of existing manufacturing processes to identify cost‑reduction opportunities; analyze operational data (usage, maintenance, efficiency, quality) and implement process improvements, policies, and procedures that support safety and quality
  • Create and manage detailed project plans to ensure timely implementation of equipment and fixtures; build strong relationships with stakeholders; support capital projects including FAT, installation, commissioning, validation, and authoring equipment documentation (URS, FRS, design specs)
  • Ensure equipment is included in preventative maintenance programs; oversee reliability initiatives; develop and implement maintenance procedures and CMMS systems; own and update preventative maintenance SOPs
  • Design and implement process improvements that enhance quality, reduce costs, increase productivity, and shorten cycle times
  • Perform other duties as assigned

The Candidate:

  • Must have a Bachelor’s Degree. Preferably in Electrical Engineering, Mechanical Engineering or related Engineering discipline with a minimum of 3-5 years’ of relevant experience in a pharmaceutical environment OR
  • High School Diploma or GED with 5-10 years of experience in equipment maintenance or related position within a pharmaceutical environment
  • Proficiency in MS Office Word, Excel, Visio and Outlook is required
  • Good Manufacturing Principles (GMP) background experience is required
  • Strong verbal and written communication skills are required
  • Individual may be required to lift, push, pull 0-40 pounds as required

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!

About Catalent Pharma Solutions Inc

Catalent Pharma Solutions Inc is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene therapies, and consumer health products. The company operates in four segments: Softgel and Oral Technologies, Biologics, Oral and Specialty Delivery, and Clinical Supply Services. Catalent Pharma Solutions serves customers in various industries, including pharmaceuticals, biotechnology, and consumer health. The company was founded in 2007 and is headquartered in Somerset, New Jersey.
Learn more about Catalent Pharma Solutions Inc
Size
14,000 employees
Industry
Founded
2007

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