ZipRecruiter

Log In

1

Associate Downstream Process Development Scientist Jobs in Middleton, WI

Ametek

R&D Scientist

Madison, WI

... D Scientist to support the design and development of next-generation Atom Probe microscopes ... Develop processes for manufacturing proprietary components used in atom probe instruments * Apply ...

Ametek

R&D Scientist

Madison, WI · On-site

... D Scientist to support the design and development of next-generation Atom Probe microscopes ... Develop processes for manufacturing proprietary components used in atom probe instruments * Apply ...

Labcorp

Method Development Scientist III

Madison, WI · On-site

Method Development Scientist - III (Madison, Wisconsin) Work schedule : Monday - Friday (Day Shift ... Contributes to evaluation of departmental procedures and local process improvements. * Promotes a ...

New

previous pagenext page

Showing results 21-40

All JobsAssociate Downstream Process Development Scientist JobsAssociate Downstream Process Development Scientist Jobs in Middleton, WI

Associate Downstream Process Development Scientist information

See Middleton, WI salary details

$19

$33

$49

How much do associate downstream process development scientist jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for associate downstream process development scientist in Middleton, WI is $33.80, according to ZipRecruiter salary data. Most workers in this role earn between $27.74 and $41.49 per hour, depending on experience, location, and employer.

What is an associate downstream process development scientist?

An Associate Downstream Process Development Scientist is a professional who works in the biotechnology or pharmaceutical industry, focusing on developing and optimizing processes that purify biological products, such as proteins or antibodies, after they have been produced by cells. Their work is crucial for ensuring the final product meets quality and safety standards before it is used in research or clinical applications. They typically perform laboratory experiments, analyze data, and collaborate with other scientists and engineers to improve yield and efficiency. This role is often entry-level or early-career, providing hands-on experience in process development and technical troubleshooting.

What are the key skills and qualifications needed to thrive as an associate downstream process development scientist, and why are they important?

To excel as an Associate Downstream Process Development Scientist, you need a solid understanding of biochemistry, chemical engineering, and downstream purification techniques, often supported by a bachelor's or master's degree in a life science or engineering discipline. Familiarity with chromatographic systems (such as AKTA), filtration equipment, and analytical tools, as well as knowledge of GMP/GLP regulations, is typically required. Strong problem-solving, attention to detail, and effective teamwork and communication skills help you navigate complex experiments and collaborate with cross-functional teams. These skills ensure efficient process optimization, compliance with regulatory standards, and successful development of biopharmaceutical products.

What is the difference between Associate Downstream Process Development Scientist vs Associate Upstream Process Development Scientist?

AspectAssociate Downstream Process Development ScientistAssociate Upstream Process Development Scientist
Primary FocusPurification and recovery of bioproductsCell culture and fermentation processes
Required SkillsProtein purification, chromatography, filtrationCell culture, bioreactor operation, media preparation
Work EnvironmentLaboratories, manufacturing facilitiesLaboratories, bioreactor labs
Common CertificationsBiotech or bioprocessing certificationsBiotech or bioprocessing certifications

Both roles are essential in biopharmaceutical development, focusing on different stages of the production process. The Associate Downstream Process Development Scientist specializes in purification techniques, while the Associate Upstream Process Development Scientist concentrates on cell growth and fermentation. Understanding these distinctions helps candidates target their skills and career paths effectively.

What are some typical challenges faced by an associate downstream process development scientist, and how can they be addressed?

Associate Downstream Process Development Scientists often encounter challenges such as optimizing purification processes, troubleshooting equipment performance, and ensuring batch-to-batch consistency. These challenges can be addressed by maintaining meticulous documentation, collaborating closely with upstream and analytical teams, and staying current with best practices in chromatography and filtration. Proactively seeking feedback from experienced colleagues and participating in cross-functional meetings can also help in identifying solutions and improving process efficiency.
Associate Downstream Process Development Scientist jobs near you
Infographic showing various Associate Downstream Process Development Scientist job openings in Middleton, WI as of August 2026, with employment types broken down into 72% Full Time, 21% Part Time, and 7% Contract. Highlights an 100% In-person job distribution, with an average salary of $70,309 per year, or $33.8 per hour.

Scientist - Process Development, Drug Substance Lifecycle

Catalent Pharma Solutions

Madison, WI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 29 days ago

Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

60th of 86 rated pharmaceutical

Job description

Scientist - Process Development, Drug Substance Lifecycle

Catalent is seeking aScientist - Process Development, Drug Substance Lifecycleto join our team in Madison, Wisconsin. In this role, you will provide technicalexpertiseand lifecycle support for biologics programs as they progress through development, validation, commercialization, and post-approval manufacturing.You'llcollaborate across Manufacturing, Quality, MS&T, Regulatory, Project Management, and client teams to drive successful program execution and continuous process improvement.

About Catalent Madison

Catalent's Madison, Wisconsin facility isa state-of-the-artbiologicsdevelopment and manufacturing site supporting customers from research through early- and mid-stage clinical production. Located at 726 Heartland Trail, the 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance manufacturing, and biopharmaceutical process development.

The site is home to Catalent's proprietaryGPEx andGPEx Lightning technologies, enabling the generation of high-producing mammalian cell lines for biologic therapies. With production capabilities ranging from 50L to 4,000L and a recent $45 million expansion, the Madison campus continues to play a critical role in Catalent's globalbiologicsnetwork while supporting Wisconsin's growing life sciences industry.

Location:100% Onsite at our facility in Madison, Wisconsin
Shift:Monday - Friday, First Shift

Key Responsibilities

  • Lead process characterization activities for development, validation, and commercial-stage biologics programs.

  • Support process validation, continued process verification, comparability assessments, and lifecycle change management.

  • Analyze process performance data,identifyimprovement opportunities, and drive risk reduction initiatives.

  • Serve as a technical subject matter expert for assigned programs and client interactions.

  • Author and review technical protocols, reports, validation documents, and regulatory support documentation.

  • Support investigations, CAPAs, change controls, and quality system activities in a cGMP environment.

  • Collaborate with cross-functional teams to ensure successful technology transfer and commercial manufacturing support.

  • Other responsibilities as needed.

Required Qualifications

  • PhD in a STEM discipline,orMaster's degree with a minimum of 3 years of relevant industryexperience,orBachelor'sdegree with a minimum of 6 years of relevant industry experience.

Preferred Qualifications

  • Experience supportingbiologicsdevelopment, characterization, validation, or commercial manufacturing.

  • Knowledge of process characterization, PPQ, lifecycle management, and validation principles.

  • Experience working withincGMPenvironments.

  • Familiarity with statistical analysis tools such as JMP, Minitab, or Excel.

  • Experience supporting cross-functional technical projects and client-facing activities.

Why you should join Catalent

  • Opportunity to play a key role in driving growth within a global CDMO leader.

  • Competitive compensation package, including incentive opportunity.

  • Day-one medical, dental, and vision coverage.

  • 401(k) with companymatch.

  • Tuition reimbursement and professional development opportunities.

  • Generous paid time off and holiday schedule (152 hours+ 8 holidays)

  • Collaborative, mission-driven culture focused on improving patient outcomes worldwide.

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

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Catalent logo

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

Social media

FacebookTwitter

View All Catalent Jobs

Apply