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Biotech Process Engineer Jobs in Madison, WI (NOW HIRING)

Senior Financial Analyst

Janesville, WI · On-site

$78K - $98K/yr

... biotech organization. Senior Financial Analyst Why This Opportunity Stands Out: * Play a key role ... processes, and capital reporting requirements. * Partner with engineering, construction, and ...

New

Senior Financial Analyst

Janesville, WI · On-site

$84K - $104K/yr

... biotech organization. Senior Financial Analyst Why This Opportunity Stands Out: * Play a key role ... processes, and capital reporting requirements. * Partner with engineering, construction, and ...

New

GMP Technical Writer

Madison, WI · On-site

$50 - $70/hr

... date processes. * Author and edit SOPs, Work Instructions,engineering procedures, and related ... biotechnology, medical device, or other regulatedmanufacturing environments. * Demonstrated ...

Summary Elephas is a growing biotechnology company located in Madison, WI seeking a talented ... Experience programming in Python is preferred * Knowledge of machine learning, data science, data ...

Summary Elephas is a growing biotechnology company located in Madison, WI seeking a talented ... Experience programming in Python is preferred * Knowledge of machine learning, data science, data ...

Summary Elephas is a growing biotechnology company located in Madison, WI seeking a talented ... Experience programming in Python is preferred * Knowledge of machine learning, data science, data ...

Showing results 41-60

Biotech Process Engineer information

See Madison, WI salary details

$49.9K

$92.7K

$143.6K

How much do biotech process engineer jobs pay per year?

As of Sep 11, 2026, the average yearly pay for biotech process engineer in Madison, WI is $92,733.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,100.00 and $103,800.00 per year, depending on experience, location, and employer.

What does a Biotech Process Engineer do?

A Biotech Process Engineer designs, develops, and optimizes processes used in the production of biological products such as pharmaceuticals, vaccines, and biofuels. They work closely with scientists and manufacturing teams to scale up lab procedures to industrial levels while ensuring product quality and regulatory compliance. Their role often involves troubleshooting equipment, improving efficiency, and implementing new technologies within biotech manufacturing environments.

What are the key skills and qualifications needed to thrive as a Biotech Process Engineer, and why are they important?

To thrive as a Biotech Process Engineer, you need a solid background in chemical or biochemical engineering, process design, and regulatory compliance, typically supported by a relevant bachelor's or master's degree. Familiarity with process control systems, bioprocess simulation software, and industry-standard quality systems such as cGMP is essential. Strong analytical thinking, problem-solving abilities, and effective teamwork and communication skills help you excel in cross-functional environments. These skills ensure efficient, compliant, and innovative bioprocess operations, which are critical for product quality and organizational success.

What are some common challenges faced by Biotech Process Engineers during scale-up from laboratory to production?

Biotech Process Engineers often encounter challenges when scaling up processes from laboratory or pilot scale to full production. These challenges can include maintaining product consistency, ensuring process sterility, and adapting equipment to handle larger volumes without compromising yield or quality. Engineers must also collaborate closely with cross-functional teams such as quality assurance, validation, and manufacturing to implement changes efficiently and adhere to regulatory standards. Proactive problem-solving and strong communication skills are key to overcoming these hurdles and ensuring successful technology transfer.

What is the difference between Biotech Process Engineer vs Biotech Manufacturing Technician?

AspectBiotech Process EngineerBiotech Manufacturing Technician
CredentialsBachelor's degree in biotech, chemical engineering, or related field; often requires experience in process designAssociate's or bachelor's degree; focus on operational skills and equipment handling
Work EnvironmentDesigning, optimizing, and overseeing production processes in labs or manufacturing facilitiesOperating and maintaining equipment on the manufacturing floor
Job FocusProcess development, scale-up, troubleshooting, and process improvementExecuting production tasks, quality checks, and equipment setup

Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

What job categories do people searching Biotech Process Engineer jobs in Madison, WI look for?

The top searched job categories for Biotech Process Engineer jobs in Madison, WI are:

Infographic showing various Biotech Process Engineer job openings in Madison, WI as of September 2026, with employment types broken down into 1% As Needed, 74% Full Time, 21% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $92,733 per year, or $44.6 per hour.

Senior Scientist I - Quality Control - Data Review

Madison, WI • On-site

Catalent, Inc.
Pharmaceutical Product Wholesalers • 10K+ employees

Full-time

Medical, Dental, Vision, Life, PTO

Posted 7 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz


Job description

Senior Scientist I - Quality Control - Data Review
Position Summary:
  • Shift: M-F 8am-5pm
  • Location: Madison, WI
  • 100% Onsite

Catalent'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.
We have an opportunity for a Senior Scientist I - Quality Control - Data Review to join our team. In this role, you will execute and document cGMP Quality Control testing with precision. You will operate equipment, review analytical data, and ensure compliance with SOPs. You will also contribute to technical documentation and support laboratory operations in a collaborative environment.
The Role:
  • Review a variety of different tests
  • Review and update Standard Operating Procedures (SOPs)
  • Perform monthly routine checks of logbooks within the lab
  • Ensure adherence to protocols and methods
  • Follow Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
  • Review analytical and microbiology data
  • Assist with training of junior staff
  • Help coordinate day-to-day tasks in the supervisor's absence
  • All other duties as assigned.

The Candidate:
  • Ph.D. in Biology, Biotechnology, Chemistry or related life sciences field OR
  • Master's degree in Biology, Biotechnology, Chemistry or related life sciences field with a minimum of 4 years of industry experience OR
  • Bachelor's degree in Biology, Biotechnology, Chemistry or related life sciences field with a minimum of 6 years of industry experience OR
  • Associate degree in Biology, Biotechnology, Chemistry or related life sciences field with a minimum of 10 years of industry experience OR
  • High School Diploma or equivalent with a minimum of 11 years of industry experience
  • Intermediate to advanced proficiency in Microsoft Office preferred
  • Familiarity with EMPOWER software preferred

Preferred Skills & Background
  • Experience with EMPOWER system used for High-Performance Liquid Chromatography (HPLC)
  • Strong background in Size Exclusion Chromatography (SEC), Capillary Electrophoresis (CE), Capillary Isoelectric Focusing (cIEF), and Reverse Phase High-Performance Liquid Chromatography (RP-HPLC)
  • Experience with Enzyme-Linked Immunosorbent Assay (ELISA) and plate-based assays
  • Knowledge of compendial methods, appearance, pH, concentration, and osmolality

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 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.

What Catalent employees say

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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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