{"schemaVersion":"jobsearcher.job.v1","id":"4b99f798e865548e7ebd0f51","url":"https://jobsearcher.com/jobs/4b99f798e865548e7ebd0f51","canonicalUrl":"https://jobsearcher.com/jobs/4b99f798e865548e7ebd0f51","title":"Process Engineer - Engineering","description":"Process Engineer - Engineering\n\nAbout Site\n\nCatalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single‑use systems to enable rapid scale‑up and customization. The site is home to Catalent’s proprietary GPEx® and GPEx® Lightning technologies, which are used to generate high‑yielding mammalian cell lines for biologic therapies, and supports production scales ranging from 50 to 4,000 liters for clinical manufacturing. Following a $45 million expansion announced in 2025, the Madison site has significantly increased capacity, added new equipment, and created approximately 200 highly skilled biohealth jobs, further strengthening its role within Catalent’s global biologics network and Wisconsin’s growing life sciences ecosystem.\n\nPosition Summary\n\nWe have an opportunity for a Process Engineer - Engineering to join our team and contribute to advancing biologics development and manufacturing. This role offers the chance to work in a dynamic environment focused on innovation and continuous improvement. You will collaborate with cross-functional teams to support process optimization, technical troubleshooting, and strategic projects. This is an exciting opportunity to make an impact on life-changing therapies while growing your career in a state-of-the-art facility.\n\nShift: Monday -Friday, 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30-minute unpaid lunch\nLocation: Madison, WI\n100% Onsite\n\nThe Role\n\nEvaluate existing processes and identify improvements to enhance efficiency, cost savings, time savings, consistency, and competitiveness.\n\nLead technical support for risk assessments, gap analysis, deviations, change controls, and corrective and preventive actions, including root-cause analysis and corrective action identification.\n\nSupport drafting and development of User Required Specifications and participate in Factory Acceptance Testing, Site Acceptance Testing, and Qualification/Validation testing for new and existing technologies.\n\nLead site strategy projects with cross-department resources and Site Leadership Team visibility through implementation.\n\nOversee technical support of Manufacturing, including change management, troubleshooting, and oversight of site strategy projects.\n\nSupport consumable and raw material lifecycle management for single-use GMP manufacturing from design through implementation.\n\nTrack, trend, and analyze data for compliance, product quality, continuous improvement, and day-to-day investigations and troubleshooting.\n\nPerform other duties as assigned.\n\nThe Candidate\n\nMinimum Requirements\n\nBachelor’s degree in Industrial, Electrical, Mechanical, Chemical, Computer Science, Civil Engineering, or related scientific/engineering field with 3+ years of facilities operation or automation engineering experience in a cGMP environment (preferably biopharmaceutical) OR\n\nMaster’s degree in Industrial, Electrical, Mechanical, Chemical, Computer Science, Civil Engineering, or related scientific/engineering field with 1+ year of facilities operation or automation engineering experience in a cGMP environment (preferably biopharmaceutical).\n\nRequires frequent sitting, standing, walking, reading documents, computer use, reaching, communication, and writing, with occasional bending, kneeling, crouching, carrying, and lifting up to 50 pounds.\n\nPreferred Skills & Background\n\nPrevious experience leading cross-department facility and/or site improvement projects is a plus.\n\nAbility to create and deliver complex reports and presentations.\n\nAbility to interpret data, analyze trends, and provide insights into potential issues and solutions.\n\nAbility to complete investigation, deviation, and change control forms independently.\n\nAbility to introduce new technology and drive process improvements, collaborating with other groups to develop, qualify, and transfer methods.\n\nExperience in writing, editing, and reviewing Standard Operating Procedures.\n\nWhy You Should Join Catalent\n\nDefined career path with annual performance reviews and feedback.\n\nDiverse and inclusive culture.\n\nOpportunities for career growth within an organization dedicated to improving lives.\n\nCompetitive paid time off plus 8 paid holidays.\n\nCommunity engagement and green initiatives.\n\nMedical, dental, and vision benefits effective from day one.\n\nTuition reimbursement program.\n\nCatalent 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.\n\npersonal initiative. dynamic pace. meaningful work.\n\nVisit Catalent Careers to explore career opportunities.\n\nCatalent is an Equal Opportunity Employer, including disability and veterans.\n\nIf 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.\n\nNotice 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.\n\nImportant Security Notice to U.S. Job Seekers:\n\nCatalent 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.\n\nCalifornia Job Seekers can find our California Job Applicant Notice HERE.","company":"Catalentpharmasolutions","rawCompany":"catalentpharmasolutions","city":"Madison","state":"WI","isRemote":false,"isActive":false,"createdAt":"2026-08-22T15:56:29.688Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer - Engineering","description":"Process Engineer - Engineering\n\nAbout Site\n\nCatalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single‑use systems to enable rapid scale‑up and customization. The site is home to Catalent’s proprietary GPEx® and GPEx® Lightning technologies, which are used to generate high‑yielding mammalian cell lines for biologic therapies, and supports production scales ranging from 50 to 4,000 liters for clinical manufacturing. Following a $45 million expansion announced in 2025, the Madison site has significantly increased capacity, added new equipment, and created approximately 200 highly skilled biohealth jobs, further strengthening its role within Catalent’s global biologics network and Wisconsin’s growing life sciences ecosystem.\n\nPosition Summary\n\nWe have an opportunity for a Process Engineer - Engineering to join our team and contribute to advancing biologics development and manufacturing. This role offers the chance to work in a dynamic environment focused on innovation and continuous improvement. You will collaborate with cross-functional teams to support process optimization, technical troubleshooting, and strategic projects. This is an exciting opportunity to make an impact on life-changing therapies while growing your career in a state-of-the-art facility.\n\nShift: Monday -Friday, 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30-minute unpaid lunch\nLocation: Madison, WI\n100% Onsite\n\nThe Role\n\nEvaluate existing processes and identify improvements to enhance efficiency, cost savings, time savings, consistency, and competitiveness.\n\nLead technical support for risk assessments, gap analysis, deviations, change controls, and corrective and preventive actions, including root-cause analysis and corrective action identification.\n\nSupport drafting and development of User Required Specifications and participate in Factory Acceptance Testing, Site Acceptance Testing, and Qualification/Validation testing for new and existing technologies.\n\nLead site strategy projects with cross-department resources and Site Leadership Team visibility through implementation.\n\nOversee technical support of Manufacturing, including change management, troubleshooting, and oversight of site strategy projects.\n\nSupport consumable and raw material lifecycle management for single-use GMP manufacturing from design through implementation.\n\nTrack, trend, and analyze data for compliance, product quality, continuous improvement, and day-to-day investigations and troubleshooting.\n\nPerform other duties as assigned.\n\nThe Candidate\n\nMinimum Requirements\n\nBachelor’s degree in Industrial, Electrical, Mechanical, Chemical, Computer Science, Civil Engineering, or related scientific/engineering field with 3+ years of facilities operation or automation engineering experience in a cGMP environment (preferably biopharmaceutical) OR\n\nMaster’s degree in Industrial, Electrical, Mechanical, Chemical, Computer Science, Civil Engineering, or related scientific/engineering field with 1+ year of facilities operation or automation engineering experience in a cGMP environment (preferably biopharmaceutical).\n\nRequires frequent sitting, standing, walking, reading documents, computer use, reaching, communication, and writing, with occasional bending, kneeling, crouching, carrying, and lifting up to 50 pounds.\n\nPreferred Skills & Background\n\nPrevious experience leading cross-department facility and/or site improvement projects is a plus.\n\nAbility to create and deliver complex reports and presentations.\n\nAbility to interpret data, analyze trends, and provide insights into potential issues and solutions.\n\nAbility to complete investigation, deviation, and change control forms independently.\n\nAbility to introduce new technology and drive process improvements, collaborating with other groups to develop, qualify, and transfer methods.\n\nExperience in writing, editing, and reviewing Standard Operating Procedures.\n\nWhy You Should Join Catalent\n\nDefined career path with annual performance reviews and feedback.\n\nDiverse and inclusive culture.\n\nOpportunities for career growth within an organization dedicated to improving lives.\n\nCompetitive paid time off plus 8 paid holidays.\n\nCommunity engagement and green initiatives.\n\nMedical, dental, and vision benefits effective from day one.\n\nTuition reimbursement program.\n\nCatalent 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.\n\npersonal initiative. dynamic pace. meaningful work.\n\nVisit Catalent Careers to explore career opportunities.\n\nCatalent is an Equal Opportunity Employer, including disability and veterans.\n\nIf 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.\n\nNotice 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.\n\nImportant Security Notice to U.S. Job Seekers:\n\nCatalent 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.\n\nCalifornia Job Seekers can find our California Job Applicant Notice HERE.","datePosted":"2026-08-22T15:56:29.688Z","dateModified":"2026-08-22T15:56:29.688Z","hiringOrganization":{"@type":"Organization","name":"Catalentpharmasolutions","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Madison","addressRegion":"WI","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"4b99f798e865548e7ebd0f51"},"url":"https://jobsearcher.com/jobs/4b99f798e865548e7ebd0f51"}}