Process Engineer

Posted Yesterday
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Kansas City, MO, USA
In-Office
Junior
Biotech • Pharmaceutical
The Role
Support clinical and commercial manufacturing by executing capital projects, developing URS, performing equipment IQ/OQ/PQ, authoring SOPs, troubleshooting processes, implementing continuous improvement (lean/6σ), and ensuring GMP, safety, and quality compliance while collaborating cross-functionally.
Summary Generated by Built In
Process EngineerAbout Site

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

Position Summary

We have an opportunity for a Process Engineer to join our team. In this role, you will support both clinical and commercial operations, including capital requests, equipment onboarding and qualification, and process optimization using lean six sigma or equivalent methods. You will manage projects, monitor processes, and ensure compliance with quality and safety standards. This position reports to the Process Engineering Manager and plays a key role in driving efficiency and continuous improvement.

Shift: 2nd shift Monday - Thursday, 1:30pm - 12:00am
Location: Kansas City, MO
100% Onsite

The Role
  • Support daily manufacturing operations by ensuring safety, quality, delivery, and cost objectives are met.
  • Assist with the development of User Requirement Specifications (URS) for new and modified equipment and processes.
  • Execute small to medium capital projects, including planning, budgeting, purchasing, installation, commissioning, and project closeout.
  • Develop and execute equipment qualification protocols (IQ/OQ/PQ) to support new equipment installations and process improvements.
  • Author and maintain SOPs, work instructions, and equipment documentation to ensure compliant and efficient operations.
  • Analyze manufacturing processes to identify bottlenecks, troubleshoot issues, and implement process improvements that increase efficiency and reliability.
  • Support integration of new and modified equipment into preventive and Total Productive Maintenance (TPM) programs.
  • Collaborate with Operations, Maintenance, Quality, and Validation teams to provide technical support for deviations, CAPAs, change controls, and continuous improvement initiatives.
  • Participate in equipment risk assessments, Gemba walks, and safety reviews to identify hazards and support corrective actions.
  • Coordinate equipment training, assist with capital expenditure forecasting, and work with vendors to evaluate, procure, and implement equipment and process solutions.
  • Perform other duties as assigned.
The CandidateMinimum Requirements
  • Bachelor’s Degree in Engineering or relevant science required.
  • 1+ years of experience in the pharmaceutical or related manufacturing industry.
  • Ability to understand Standard Operating Procedures and current Good Manufacturing Practices as necessary to accomplish daily tasks.
  • Understanding of manufacturing equipment and controls, including programmable logic controllers (PLCs), servo motors, control systems, and pneumatics.
  • Strong verbal and written communication skills with the ability to interact effectively with internal and external stakeholders.
  • Demonstrated active listening, problem-solving, decision-making, organizational, and prioritization skills in a fast-paced environment.
  • Collaborative team player with a flexible, adaptable approach and the ability to work cooperatively across functional groups.
  • Physical Requirements: Frequently requires standing, walking, sitting, kneeling, and reaching; occasionally requires lifting, pushing, and pulling up to 45 lbs.
  • Working Environment: Occasional exposure to extreme cold, extreme heat, humidity, wet conditions, noise, hazards, temperature changes, and vibration.
Preferred Skills & Background
  • Bachelor’s Degree in Chemical Engineering or Mechanical Engineering.
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.
  • Competitive paid time off plus 8 paid holidays.
  • Community engagement and green initiatives.
  • Medical, dental, and vision benefits effective day one of employment.
  • Tuition reimbursement.

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 [email protected]. 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.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [email protected] for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

Skills Required

  • Bachelor's Degree in Engineering or relevant science
  • 1+ years of experience in the pharmaceutical or related manufacturing industry
  • Understanding of Standard Operating Procedures and current Good Manufacturing Practices (cGMP)
  • Understanding of manufacturing equipment and controls (PLCs, servo motors, control systems, pneumatics)
  • Experience with equipment qualification protocols (IQ/OQ/PQ) and developing User Requirement Specifications (URS)
  • Ability to author and maintain SOPs, work instructions, and equipment documentation
  • Strong verbal and written communication skills
  • Demonstrated problem-solving, decision-making, organizational, and prioritization skills in a fast-paced environment
  • Collaborative team player with flexibility and ability to work across functional groups
  • Physical ability to frequently stand, walk, kneel and occasionally lift/push/pull up to 45 lbs
  • Willingness/ability to work 2nd shift (Mon-Thu 1:30pm-12:00am) and be 100% onsite in Kansas City, MO
  • Bachelor's Degree in Chemical Engineering or Mechanical Engineering

Catalent, Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Catalent, Inc. and has not been reviewed or approved by Catalent, Inc..

  • Leave & Time Off Breadth Paid time off is commonly described as roughly 152 hours per year plus about eight paid holidays for U.S. roles. Eligibility and exact counts vary by location, but the allotment is positioned as competitive.
  • Retirement Support A 401(k) with a company match (often described as dollar‑for‑dollar up to 6%) is part of the package. The match level is commonly referenced as a meaningful component of total rewards.
  • Inclusive Benefits Coverage Medical, dental, vision, life/disability, HSA/FSA, EAP, tuition reimbursement, adoption assistance, commuter and dependent‑care benefits, and wellness programs are offered. Some roles indicate benefits eligibility begins on the first day for direct hires.

Catalent, Inc. Insights

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The Company
HQ: Tampa, FL
13,715 Employees
Year Founded: 2007

What We Do

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. For more information, visit www.catalent.com.

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