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Associate Pvd Process Engineer Jobs in Stoughton, WI

Paper Converting Machine

Senior Quality Engineer

Madison, WI · On-site

$89K - $120K/yr

Lead process audits and other quality systems related projects. * Understand details of engineering ... LEADERSHIP RESPONSIBILITY This position does not directly supervise other associates. WORK ...

Ametek

R&D Scientist

Madison, WI

... engineers to design, procure, and test prototype systems Manufacturing & Process Development ... PVD) * Experience with machine shop tools (CNC mill, lathe, hand tools) * Proficiency with lab ...

Barry Wehmiller Group

Senior Quality Engineer

Madison, WI

$89K - $120K/yr

Lead process audits and other quality systems related projects. * Understand details of engineering ... LEADERSHIP RESPONSIBILITY This position does not directly supervise other associates. WORK ...

Ametek

R&D Scientist

Madison, WI · On-site

... engineers to design, procure, and test prototype systems Manufacturing & Process Development ... PVD) * Experience with machine shop tools (CNC mill, lathe, hand tools) * Proficiency with lab ...

System One

Databricks Engineer

Madison, WI · On-site

... processing-time). • Observability skills: logging/metrics/alerting, troubleshooting, and ... Databricks Certified Apache Spark Developer Associate ? Databricks Certified Data Engineer ...

Kellton Tech

Manufacturing Engineer

Madison, WI · On-site

$73K - $94K/yr

Manufacturing Engineer Location: Onsite - Madison, WI Pay Rate: 48-54/hr. (W2) Job Summary The ... Train and guide production associates on new and existing processes, equipment, and documentation.

NOVARES

Automation Engineer

Janesville, WI · On-site

Analyze production processes and identify opportunities for automation and process optimization ... Associate degree with significant automation engineering experience may be considered.5+ years of ...

Novares

Automation Engineer

Janesville, WI

Analyze production processes and identify opportunities for automation and process optimization ... Associate degree with significant automation engineering experience may be considered.5+ years of ...

United Alloy, Inc.

Quality Engineer

Janesville, WI · On-site

$64K - $82K/yr

Certified Quality Engineer (CQE), Certified Six Sigma Green Belt (CSSGB) or Certified Quality Improvement Associate (CQIA) • Solid understanding of quality systems, inspection and testing processes ...

FAIRBANKS MORSE DEFENSE

Manufacturing Engineer

Beloit, WI · On-site

$69K - $89K/yr

Participate in the development of processes, tooling, fixtures, setups, and CNC machine programs ... Associate degree in Manufacturing, Industrial or Mechanical or technical field or. * Ability work ...

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All JobsAssociate Pvd Process Engineer JobsAssociate Pvd Process Engineer Jobs in Stoughton, WI

Associate Pvd Process Engineer information

See Stoughton, WI salary details

$47.9K

$89K

$137.8K

How much do associate pvd process engineer jobs pay per year?

As of Aug 5, 2026, the average yearly pay for associate pvd process engineer in Stoughton, WI is $88,966.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $99,600.00 per year, depending on experience, location, and employer.

What is the difference between Associate Pvd Process Engineer vs Chemical Process Engineer?

AspectAssociate Pvd Process EngineerChemical Process Engineer
CredentialsBachelor's in Materials, Chemical, or Mechanical Engineering; some roles may require certifications in PVD processesBachelor's or higher in Chemical Engineering; professional engineering license may be preferred
Work EnvironmentCleanroom or manufacturing settings focused on thin film deposition using PVD techniquesIndustrial plants, chemical manufacturing, or R&D labs involving chemical reactions and process optimization
Industry UsageElectronics, semiconductor, optics, and coating industriesPetrochemical, pharmaceuticals, specialty chemicals, and process industries

The Associate Pvd Process Engineer primarily focuses on thin film deposition using physical vapor deposition techniques within electronics and coating industries. In contrast, a Chemical Process Engineer works on chemical reactions and process optimization across various chemical manufacturing sectors. While both roles require a background in chemical or materials engineering, their work environments and industry applications differ significantly.

What are some common challenges faced by Associate PVD Process Engineers, and how can they be addressed?

Associate PVD Process Engineers often encounter challenges such as maintaining consistent thin film quality, troubleshooting equipment malfunctions, and optimizing process parameters for yield improvement. Addressing these challenges typically involves collaborating closely with cross-functional teams like equipment engineers and quality assurance, conducting root-cause analyses, and staying updated on best practices and new technologies. Regular training, hands-on experience, and open communication with senior engineers and production staff can help new associates quickly build problem-solving skills and adapt to the dynamic cleanroom environment.

What are the key skills and qualifications needed to thrive as an Associate PVD Process Engineer?

To thrive as an Associate PVD Process Engineer, you typically need a bachelor's degree in materials science, chemical engineering, or a related field, along with a solid understanding of thin film deposition and vacuum technology. Familiarity with sputtering, evaporation systems, and process control software is essential, and certifications in semiconductor manufacturing or equipment operation can be advantageous. Strong analytical thinking, problem-solving skills, and effective teamwork enhance performance in this role. These competencies are crucial to ensure efficient process development, troubleshooting, and maintaining high-quality production in advanced manufacturing environments.

What is an Associate PVD Process Engineer?

Associate PVD (Physical Vapor Deposition) Process Engineers are entry-level professionals who help develop, optimize, and maintain PVD processes used to deposit thin films onto substrates in industries like semiconductor manufacturing. They work under the guidance of senior engineers, assisting with process development, troubleshooting equipment, running experiments, and analyzing data to improve film quality and production efficiency. Their role is crucial in ensuring consistent product quality and supporting the overall manufacturing process.
What are popular job titles related to Associate Pvd Process Engineer jobs in Stoughton, WI? For Associate Pvd Process Engineer jobs in Stoughton, WI, the most frequently searched job titles are:
What cities near Stoughton, WI are hiring for Associate Pvd Process Engineer jobs? Cities near Stoughton, WI with the most Associate Pvd Process Engineer job openings:
Associate Pvd Process Engineer jobs near you
Infographic showing various Associate Pvd Process Engineer job openings in Stoughton, WI as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $88,966 per year, or $42.8 per hour.

Process Engineer - Manufacturing Sciences & Technology

Catalent, Inc.

Madison, WI • On-site

$74K - $98K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 days ago

Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

59th of 86 rated pharmaceutical

Job description

Process Engineer - Manufacturing Sciences & Technology (MS&T), Downstream Technology Transfer
Position Summary:
  • Work Schedule: Monday - Friday, core hours 8am-5pm
  • 100% on-site (Madison, WI)

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.
The Process Engineer for MS&T supports the department which serves as an agile technical services organization supporting process and technology transfer between Process Development (internal and external) and at-scale GMP manufacturing. The Technology Transfer groups (Upstream and Downstream) act as the primary technical liaisons, ensuring successful transfer and execution of biologic processes across a range of modalities, including monoclonal antibodies, fusion proteins, enzymes, mRNA, and emerging technologies. Department responsibilities include process modeling, facility fit assessments, initial bill-of-materials development, and evaluation of equipment and consumables, as well as authoring and supporting critical manufacturing documentation such as gap assessments, technical reports, product impact assessments, and batch records. MS&T also provides hands-on process readiness and execution support to enable robust, compliant, and scalable manufacturing operations.
The Role:
  • Downstream Tech Transfer Duties: Provide technical support to Manufacturing, leading facility fit, equipment alignment, and technology transfer of biologic processes from Process Development and external clients. Evaluate and recommend process and equipment improvements while supporting technology transfer for both internally and externally developed manufacturing processes.
  • Execute technical work plans and schedules, including data generation and entry, in collaboration with supervisors or senior team members. Perform engineering and process calculations to support development, tech transfer, and GMP manufacturing programs.
  • Draft, author, and review technical documentation, including development reports, technical transfer reports, batch production records, engineering specifications, and summary reports.
  • Conduct parallel technical reviews of laboratory and engineering documentation to ensure accuracy, completeness, and regulatory compliance.
  • Support GMP manufacturing through technical oversight, batch documentation authoring, and close collaboration with Manufacturing teams. Lead or support risk assessments, gap analyses, deviations, change controls, and CAPAs, including root cause analysis and impact assessment.
  • Evaluate existing processes and identify process or equipment improvement opportunities to enhance efficiency, consistency, and operational competitiveness.
  • Compile, analyze, and communicate process and project data, including status reporting, trend analysis, and internal or client-facing presentations.
  • Partner cross-functionally with Process Development, Manufacturing, Quality Assurance, Quality Control, Supply Chain, Project Management, Facilities, and other stakeholders to enable effective process transfer and sustainment. Support strategic alignment and knowledge sharing across sites, including coordination with Madison and other Catalent Biologics locations.
  • Participate in client meetings, providing technical expertise and program support. Train, mentor, and coach junior staff on laboratory, manufacturing, and engineering principles; serve as a subject matter expert.
  • Other duties as assigned

The Candidate:
  • Must have a minimum of Associate's degree in STEM with 6+ years of related experience. It is preferred to have a Bachelor's and/or Master's with at least 3+ years of related experience.
  • Related experience encompasses mRNA product development experience, mRNA manufacturing, protein therapeutics MFG, and late stage/commercial MFG.
  • Demonstrated experience authoring, revising, and reviewing technical documentation, including reports, standard operating procedures (SOPs), and batch production records, supported by statistical data analysis and reporting.
  • Proven leadership experience managing and mentoring staff, including cross-functional training, personnel development, and organizational team support.
  • Hands-on experience investigating, resolving, and closing deviations, OOS events, change controls, and CAPAs in a cGMP-regulated environment.
  • Technical subject matter expertise in upstream (e.g., mammalian cell culture, IVT) and/or downstream biologics manufacturing processes (e.g., filtration, chromatography, TFF, viral filtration), including facility fit, process scaling, and technology transfer across cGMP production scales.
  • Operational engineering experience supporting late-phase, PPQ, and commercial programs, including design, onboarding, qualification, operation, and troubleshooting of single-use systems, consumables, and manufacturing equipment for biologics and molecular therapeutics.
  • Physical requirements: Individual must be able to see, hear, read, and write clear English. Frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities.

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!

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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