Experienced in all aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones. * Well organized with ability to handle and ...
Experienced in all aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones. * Well organized with ability to handle and ...
Experienced in all aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones. * Well organized with ability to handle and ...
Experienced in all aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones. * Well organized with ability to handle and ...
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 ...
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 ...
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 ...
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 ...
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
Quick apply
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams. Responsibilities * Lead post-approval change ...
This role supports analytical testing for drug substance and drug product development. The individual will perform routine laboratory testing, assist with analytical method development and ...
Quick apply
This role supports analytical testing for drug substance and drug product development. The individual will perform routine laboratory testing, assist with analytical method development and ...
An Associate Scientist III will support method development/validation activities for new drug substances and drug product. They will also support testing required for GLP Toxicology and cGMP Clinical ...
Quick apply
An Associate Scientist III will support method development/validation activities for new drug substances and drug product. They will also support testing required for GLP Toxicology and cGMP Clinical ...
Associate Scientist I, CMC Analytical Development
Verona, WI · On-site
$57K - $68K/yr
This role supports analytical testing for drug substance and drug product development. The individual will perform routine laboratory testing, assist with analytical method development and ...
Associate Scientist I, CMC Analytical Development
Verona, WI · On-site
$57K - $68K/yr
This role supports analytical testing for drug substance and drug product development. The individual will perform routine laboratory testing, assist with analytical method development and ...
Associate Scientist III, CMC Analytical Development
Verona, WI · On-site
$78K - $90K/yr
An Associate Scientist III will support method development/validation activities for new drug substances and drug product. They will also support testing required for GLP Toxicology and cGMP Clinical ...
Associate Scientist III, CMC Analytical Development
Verona, WI · On-site
$78K - $90K/yr
An Associate Scientist III will support method development/validation activities for new drug substances and drug product. They will also support testing required for GLP Toxicology and cGMP Clinical ...
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
Quick apply
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
Senior Scientist - Downstream Process Development, mRNA
Madison, WI · On-site
$92K - $126K/yr
Collaborate with analytical teams for method development and validation of mRNA drug substance. Experience authoring or reviewing method validation/qualification strategy and understanding ...
Senior Scientist - Downstream Process Development, mRNA
Madison, WI · On-site
$92K - $126K/yr
Collaborate with analytical teams for method development and validation of mRNA drug substance. Experience authoring or reviewing method validation/qualification strategy and understanding ...
Director, Pharmacometrics & Clinical Pharmacology
Madison, WI · On-site
$230 - $255/hr
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
New
Director, Pharmacometrics & Clinical Pharmacology
Madison, WI · On-site
$230 - $255/hr
Lead model-informed drug development strategies, including population PK/PD analyses, exposure-response analyses, translational modeling, dose optimization, and quantitative interpretation of ...
New
Senior Scientist I, DMPK
$115K - $140K/yr
Demonstrated experience in drug development and understanding of regulatory processes. * Excellent interpersonal, verbal, and written communication skills, with the ability to interpret and present ...
Quick apply
Senior Scientist I, DMPK
$115K - $140K/yr
Demonstrated experience in drug development and understanding of regulatory processes. * Excellent interpersonal, verbal, and written communication skills, with the ability to interpret and present ...
Senior Scientist I, DMPK
Madison, WI · On-site
$115K - $140K/yr
Demonstrated experience in drug development and understanding of regulatory processes. * Excellent interpersonal, verbal, and written communication skills, with the ability to interpret and present ...
Senior Scientist I, DMPK
Madison, WI · On-site
$115K - $140K/yr
Demonstrated experience in drug development and understanding of regulatory processes. * Excellent interpersonal, verbal, and written communication skills, with the ability to interpret and present ...
Senior Scientist II, Translational Biomarkers
Madison, WI · On-site
$125K - $140K/yr
The Position This Senior Scientist will be part of a team responsible for delivery of translational biomarker strategies for drug development candidates. The ideal candidate will possess in-depth ...
Senior Scientist II, Translational Biomarkers
Madison, WI · On-site
$125K - $140K/yr
The Position This Senior Scientist will be part of a team responsible for delivery of translational biomarker strategies for drug development candidates. The ideal candidate will possess in-depth ...
Senior Scientist II, Translational Biomarkers
$125K - $140K/yr
The Position This Senior Scientist will be part of a team responsible for delivery of translational biomarker strategies for drug development candidates. The ideal candidate will possess in-depth ...
Quick apply
Senior Scientist II, Translational Biomarkers
$125K - $140K/yr
The Position This Senior Scientist will be part of a team responsible for delivery of translational biomarker strategies for drug development candidates. The ideal candidate will possess in-depth ...
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 ...
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 ...
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 ...
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 ...
Drug Development information
See Madison, WI salary details
$33.3K - $42.4K
2% of jobs
$42.4K - $51.6K
8% of jobs
$58.6K is the 25th percentile. Wages below this are outliers.
$51.6K - $60.7K
19% of jobs
$60.7K - $69.9K
20% of jobs
The median wage is $70.2K / yr.
$69.9K - $79.1K
16% of jobs
$86.1K is the 75th percentile. Wages above this are outliers.
$79.1K - $88.2K
13% of jobs
$88.2K - $97.4K
5% of jobs
$97.4K - $106.5K
11% of jobs
$106.5K - $115.7K
2% of jobs
$115.7K - $124.9K
2% of jobs
$124.9K - $134K
2% of jobs
$33.3K
$78K
$134K
How much do drug development jobs pay per year?
What is drug development?
What are the typical stages of collaboration between different teams in a drug development role?
What are the key skills and qualifications needed to thrive in drug development, and why are they important?
What is the difference between Drug Development vs Pharmacologist?
| Aspect | Drug Development | Pharmacologist |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields; often requires experience in clinical trials | Degree in Pharmacology, Pharmacy, or related fields; may require licensing or certification for clinical practice |
| Work Environment | Research labs, pharmaceutical companies, clinical trial sites | Research labs, hospitals, academic institutions, regulatory agencies |
| Industry Usage | Developing new drugs, overseeing clinical trials, regulatory submissions | Studying drug effects, mechanisms, safety, and efficacy; advising on drug use |
While both roles are integral to the pharmaceutical industry, Drug Development focuses on creating and bringing new drugs to market through research, testing, and regulatory processes. Pharmacologists primarily study how drugs interact with biological systems, often working in research or clinical settings to understand drug effects and safety. The two roles often collaborate but differ in their core responsibilities and career focus.
How do you get into drug development?
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The top searched job categories for Drug Development jobs in Madison, WI are:
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Cities near Madison, WI with the most Drug Development job openings:

Full-time
Medical, Dental, Vision, Life, PTO
Re-posted yesterday
Catalent rating
7.6
Based on 55 frontline employees who took The Breakroom Quiz
59th of 86 rated pharmaceutical
Job description
Position Summary:
Catalent's Madison facility is a state-of-the-art biologics development and manufacturing site focused on delivering advanced solutions for biopharmaceutical products. The site features modern laboratories and flexible manufacturing spaces designed to support a wide range of biologics programs, from early development through commercial production. With cutting-edge technology and a collaborative environment, the Madison location plays a key role in driving innovation and quality in the life sciences industry. This dynamic setting offers employees the opportunity to work on impactful projects that help bring life-changing therapies to patients worldwide.
We have an opportunity for a Director, Process Development, to join our team and lead the Process Development organization. This role is responsible for advancing biologics process development from early-phase programs through commercial readiness while ensuring successful transfer into manufacturing. You will deliver scalable upstream and downstream processes, support manufacturing execution, and align cross-functional teams and clients to meet development timelines and business objectives. This position provides technical, operational, and people leadership across multiple functions and sites, driving strategic initiatives, process improvements, and organizational performance.
Location: Madison, WI
100% Onsite
The Role:
- Work closely with the Manufacturing Sciences group to ensure successful transfer of processes from PD into manufacturing in order to support early phase through commercial manufacturing activities.
- Work closely with prospective and existing clients, as well as Project Management, to ensure client expectations, scheduling, and timelines are met.
- Apply technical, functional, business, and industry expertise to design experiments and define project scopes; provide scientific and strategic consultation to site and executive leadership; and lead multiple functions and focus areas across site disciplines.
- Actively define and execute on strategic direction of the department by recommending expansion or curtailment of investigations based on experimental results or scientific information.
- Lead Process Development teams and manage 2-10 direct reports which may include principal level scientists and people leaders.
- Support manufacturing through process transfer, technology transfer, investigations, and facility fit assessments.
- Direct the development of scalable processes to support optimal expression, purification, and product quality attributes for both antibodies, recombinant proteins, and other biomolecules.
- Responsible for execution of production batches and supporting manufacturing up to sX2000L scale in SUBs.
- Identify, evaluate, and execute on process improvements to increase existing capabilities.
The Candidate:
- Bachelor's degree in STEM discipline with 15 years of biopharmaceutical manufacturing experience; OR Master's degree with 12 years' experience; OR PhD with 8 years' experience and 6+ years in leadership roles.
- Able to combine and interpret data from multiple disciplines and has a commanding understanding of the full Biologics process.
- Experienced in all aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones.
- Well organized with ability to handle and direct multiple activities within the site or across multiple sites simultaneously.
- Excellent written and verbal communication skills with internal and external customers.
- Ability to communicate complex technical information to non-technical audiences.
- Demonstrable leadership experience at Catalent (including but not limited to participation in Catalentsponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
Preferred Skills & Background
- Expertise in mammalian cell culture and upstream process development.
- Expertise in downstream process development and process characterization.
- Experience supporting technology transfer and commercial manufacturing readiness.
- Strong stakeholder management and executive influence skills.
- Strong coaching, mentoring, and talent development capabilities.
- Experience leading customer-facing technical discussions and issue resolution.
- Experience supporting production in single-use bioreactor environments.
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.
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