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Project Manager Biotech Jobs in Madison, WI (NOW HIRING)

Merck Group

Purchasing & Planning Supervisor

Madison, WI · On-site

$74K - $111K/yr

Collaborate with Project management, Manufacturing and other departments to ensure timely product ... Laboratory management with the pharmaceutical, biotechnology or manufacturing sectors. * 2+ years ...

Danaher

Health & Safety Program Manager

Madison, WI

$91K - $100K/yr

... biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our ... Strong analytical and project management skills. * Strong leadership and excellent in communication ...

Genus PLC

Early Career Lab Assistant

Rio, WI

$26.50/hr

... Biotechnology Laboratory Technician Associate Degree program at MATC or the 450 hours of work ... Our Early Career Program Manager will work with your manager to help ensure YA documentation ...

Genus PLC

Early Career Lab Assistant

Rio, WI · On-site

$26.50/hr

... Biotechnology Laboratory Technician Associate Degree program at MATC or the 450 hours of work ... Our Early Career Program Manager will work with your manager to help ensure YA documentation ...

Genus plc

Early Career Lab Assistant

Windsor, WI · On-site

$26.50/hr

... Biotechnology Laboratory Technician Associate Degree program at MATC or the 450 hours of work ... Our Early Career Program Manager will work with your manager to help ensure YA documentation ...

Genus PLC

Early Career Lab Assistant

Windsor, WI · On-site

$26.50/hr

... Biotechnology Laboratory Technician Associate Degree program at MATC or the 450 hours of work ... Our Early Career Program Manager will work with your manager to help ensure YA documentation ...

Genus PLC

Early Career Lab Assistant

Rio, WI · On-site

$26.50/hr

... Biotechnology Laboratory Technician Associate Degree program at MATC or the 450 hours of work ... Our Early Career Program Manager will work with your manager to help ensure YA documentation ...

Genus plc

Early Career Lab Assistant

Rio, WI · On-site

$26.50/hr

... Biotechnology Laboratory Technician Associate Degree program at MATC or the 450 hours of work ... Our Early Career Program Manager will work with your manager to help ensure YA documentation ...

Abbott

Sr. Controls Engineer

Madison, WI · On-site

$97K - $129K/yr

... R&D, biotech, or similar industries. * 3 years of experience as a controls engineer working with ... Experience managing and executing projects of various sizes and scopes and communicating to cross ...

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Project Manager Biotech information

See Madison, WI salary details

$22

$46

$77

How much do project manager biotech jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for project manager biotech in Madison, WI is $46.60, according to ZipRecruiter salary data. Most workers in this role earn between $40.43 and $51.11 per hour, depending on experience, location, and employer.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.
What are popular job titles related to Project Manager Biotech jobs in Madison, WI? For Project Manager Biotech jobs in Madison, WI, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Madison, WI look for? The top searched job categories for Project Manager Biotech jobs in Madison, WI are:
What cities near Madison, WI are hiring for Project Manager Biotech jobs? Cities near Madison, WI with the most Project Manager Biotech job openings:
Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Madison, WI as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $96,932 per year, or $46.6 per hour.

Purchasing & Planning Supervisor

Merck Group

Madison, WI • On-site

$74K - $111K/yr

Full-time

Medical, Retirement, PTO

Re-posted 12 days ago

Job description

Work Location: Madison, Wisconsin
Shift:
Department: LS-SC-UYWL Supply Chain
Hiring Manager: Kim Eckmayer
This information is for internals only. Please do not share outside of the organization.
Your Role:
We are seeking a highly skilled and motivated leader to join our Supply chain team within the Life Sciences division. In this role, you will supervise team and managing the daily operations of the Planning, Scheduling and Purchasing teams, ensuring that all activities are carried out in a timely, efficient and safe manner. This includes and is not limited to internal and external purchasing, planning and scheduling. The supervisor is responsible for adherence to all company operating procedures and government regulations (ISO, GMP, OSHA, DEA, CFR, etc.) You will act as the subject matter expert for the department and support internal and external projects being developed and brought into production. You will collaborate with cross-functional teams to deliver service and support to both our internal and external customers. You will deliver training and guidance to your team and others on use of multiple electronic systems (ERP, EQMS, LMS, TNA etc.) to support day to day operations to ensure smooth operations and delivery of goods and services.
  • Interface with electronic systems (ERP, EQMS, LMS, TNA) to support daily operations and ensure optimal processes.
  • Supervise team activities, including purchasing, planning, scheduling, and ensure training is complete.
  • Lead the maintenance of planning and purchasing systems (SAP - PRP, APO, EWM) and support S&OP for supply-demand alignment to Maintain raw materials and finished goods availability to meet production schedules and client forecasts.
  • Develop and implement standard operating procedures and train the team on quality management systems to compliance with policies.
  • Identify trends and implement solutions for supply chain issues; manage MRP usage for GMP and non-GMP materials.
  • Collaborate with Project management, Manufacturing and other departments to ensure timely product availability. Serve as the subject matter expert for Supply Chain/Purchasing activities related to onboarding new products and projects, also represents the department during audits and client visits.
  • Drive continuous process improvement initiatives to enhance operational efficiency and reduce costs.
  • Participate in talent selection, performance management, and employee relations through effective communication.

Who You Are
Minimum Qualifications:
  • Bachelor's degree in Supply Chain Management, Logistics, Biology, Chemistry or other Business or Life Sciences discipline.
  • 4+ years of operational experience in inventory control, planning/scheduling, or purchasing
  • 2+ years of experience in a GMP environment.

OR
  • High School Diploma or GED
  • 8+ years of experience in supply chain operations, inventory control, planning/scheduling, or purchasing. Laboratory management with the pharmaceutical, biotechnology or manufacturing sectors.
  • 2+ years of experience in a GMP environment.

Preferred Qualifications:
  • 3+ years of experience in SAP (PRP, and PSE/EWM)
  • 2+ years of experience utilizing quality management systems (Agile, Trackwise etc.)
  • Proven track record of leading a team to successfully deliver exceptional outcomes.
  • Excellent analytical, problem-solving and communication skills.
  • Work collaboratively in a cross functional fast paced environment.
  • Experience in a contract manufacturing or make to order (MTO) production environment.

Pay Range for this position: $74,300--$111,500
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.
RSREMD
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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