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Pharma Validation Engineer Jobs in Wisconsin (NOW HIRING)

Catalent Pharma Solutions in Madison, WI is hiring Facilities Engineer. This position will work on ... a valid written & signed search agreement, will become the sole property of Catalent. No fee will ...

Catalent Pharma Solutions in Madison, WI is hiring a Manager - Engineering. The Equipment ... Manage drafting and completion of validation and onboarding documents including but not limited to ...

Process Engineer

Janesville, WI · On-site

$95K - $115K/yr

... and beverage, pharma, dairy, and more. With over 18,000 employees worldwide and a strong U.S ... Will be traveling 75% of the time in North America, need a valid passport, prefer ability to travel ...

Process Engineer

Janesville, WI · On-site

$95K - $115K/yr

... and beverage, pharma, dairy, and more. With over 18,000 employees worldwide and a strong U.S ... Will be traveling 75% of the time in North America, need a valid passport, prefer ability to travel ...

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How much do pharma validation engineer jobs pay per hour?

As of May 28, 2026, the average hourly pay for pharma validation engineer in Wisconsin is $52.48, according to ZipRecruiter salary data. Most workers in this role earn between $39.81 and $63.80 per hour, depending on experience, location, and employer.

What is a Pharma Validation Engineer job?

A Pharma Validation Engineer ensures that manufacturing processes, equipment, and systems in the pharmaceutical industry comply with regulatory standards such as FDA, GMP, and ISO. They develop validation protocols, conduct tests, analyze data, and generate reports to ensure consistent product quality and safety. Their role is critical in minimizing risks, maintaining compliance, and supporting regulatory audits.

What are the key skills and qualifications needed to thrive in the Pharma Validation Engineer position, and why are they important?

To thrive as a Pharma Validation Engineer, you need a solid background in engineering or life sciences, with expertise in validation protocols, regulatory compliance (such as FDA or EMA guidelines), and Good Manufacturing Practices (GMP). Experience with validation software (like ValGenesis or MasterControl), statistical analysis tools, and relevant certifications (such as Six Sigma or ISPE) is highly valued. Strong attention to detail, project management abilities, and effective communication skills are crucial for this role. These competencies ensure validation activities meet strict regulatory standards, support product quality, and facilitate seamless cross-functional collaboration in the pharmaceutical industry.

What does a typical day look like for a Pharma Validation Engineer?

A typical day for a Pharma Validation Engineer involves developing and executing validation protocols for manufacturing equipment, laboratory instruments, or processes, ensuring they meet all regulatory and quality standards. You might collaborate closely with QA teams, production staff, and external vendors to troubleshoot issues, review data, and document results for compliance audits. Preparing detailed reports, participating in cross-functional meetings, and staying updated with current regulatory changes are also common responsibilities. This dynamic environment offers opportunities to work on diverse projects and continually expand your technical expertise while supporting product safety and efficacy.
What are the most commonly searched types of Pharma Validation Engineer jobs in Wisconsin? The most popular types of Pharma Validation Engineer jobs in Wisconsin are:
What are popular job titles related to Pharma Validation Engineer jobs in Wisconsin? For Pharma Validation Engineer jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching Pharma Validation Engineer jobs in Wisconsin look for? The top searched job categories for Pharma Validation Engineer jobs in Wisconsin are:
Engineer - Engineering

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago


Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

45th of 70 rated pharmaceutical


Job description

Engineer (Facilities)

Position Summary:

  • Work Schedule: M-F 8am-5pm
  • 100% on-site

Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics.

Catalent Pharma Solutions in Madison, WI is hiring Facilities Engineer. This position will work on complex facility-related problems requiring in-depth data analysis to determine appropriate action. The Engineer is expected to have extensive ongoing communication with employees and cross-functional group managers/departments on facility-related issues.

The Role:

  • Support the utility systems facility, including HVAC systems, process utilities, and bio-containment systems
  • Assess current and future state of site utility system capacity and utilization for improvement and maturity projects
  • Draft SOPs for building operation and maintenance
  • Provide engineering guidance and execution on facilities projects
  • Perform hands-on activities as needed to help troubleshoot facility problems and support facility staff
  • Drive continuity and development of standards in Facility Engineering to ensure smooth and effective communication flow between internal resources and customers, operational efficiency, and equipment and personnel safety
  • Create and maintain all aspects of facility design files
  • Maintain facility compliance in accordance with the site quality management system
  • Guide the specification and selection of manufacturing/utility equipment to support site facility/ process needs
  • All other duties as assigned

The Candidate:

  • Minimum B.S. degree in Industrial, Electrical, Mechanical or related scientific/engineering field with 3+ years' facilities operation/automation engineering experience in a cGMP environment (preferably biopharmaceutical)

OR

  • M.S. degree in Industrial, Electrical, Mechanical, Chemical, Computer Science, Civil Engineering, or related scientific/engineering field with 1+ years' facilities operation/automation engineering experience in a cGMP environment (preferably biopharmaceutical)
  • Previous experience leading cross-department facility and/or site improvement projects, a plus
  • Building automation systems (BAS) experience preferred

Why you should join Catalent:

  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Positive working environment focusing on continually improving processes to remain innovative
  • 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 effective day one of employment
  • Tuition Reimbursement- Let us help you finish your degree or start a new degree!

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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities.

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


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About Catalent

Sourced by ZipRecruiter

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.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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