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Project Manager Cdmo Jobs in Wisconsin (NOW HIRING)

Packaging Operator

Stevens Point, WI

$16.50 - $20/hr

... CDMO) with locations across North America and Italy. We offer a wide range of manufacturing ... project management, human resources, and environmental health and safety. Position Packaging ...

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Project Manager Cdmo information

What is a Project Manager CDMO?

A Project Manager CDMO (Contract Development and Manufacturing Organization) is responsible for overseeing pharmaceutical or biotech projects outsourced to CDMOs. They coordinate between clients and internal teams to ensure timely delivery, quality, and compliance with regulatory standards. Their role includes managing project timelines, budgets, and resources, as well as communicating progress and addressing issues that may arise during drug development and manufacturing processes.

What are the key skills and qualifications needed to thrive as a Project Manager in a CDMO (Contract Development and Manufacturing Organization), and why are they important?

To excel as a Project Manager in a CDMO, you need a strong background in project management, life sciences, and regulatory compliance, often supported by a relevant degree and PMP certification. Familiarity with project management software (like MS Project or Smartsheet), quality management systems, and industry-specific regulations such as GMP are typically required. Outstanding organizational, communication, and stakeholder management skills help you effectively coordinate cross-functional teams and client expectations. These competencies are vital for delivering complex projects on time and within budget while maintaining regulatory standards and client satisfaction.

How does a Project Manager at a CDMO typically coordinate between clients and internal teams throughout a project lifecycle?

A Project Manager at a Contract Development and Manufacturing Organization (CDMO) acts as the central point of contact for clients and internal teams, ensuring clear communication and alignment of project goals. They regularly facilitate meetings, track project milestones, and proactively address potential issues or changes in scope. This involves close collaboration with departments such as R&D, manufacturing, quality assurance, and regulatory affairs to meet client expectations and project timelines. Effective project managers also document progress and maintain transparent reporting to both clients and internal stakeholders.
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Project Manager - Engineering

Full-time

Medical, Life, Retirement, PTO

Posted 12 days ago


Catalent rating

7.4

Company rating: 7.4 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

53rd of 73 rated pharmaceutical


Job description

Project Manager - Engineering

Position Summary

  • Shift: Monday - Friday 8:00am - 5:00pm
  • 100% on-site

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

The Engineering Project Manager partners with project teams to ensure projects are completed on-time, on-schedule, and right-first-time. The project manager also ensures costs and schedules are correctly forecasted and communicated. This is accomplished by interfacing with multiple internal and external stakeholders, including vendors, contractors, Catalent Madison site leadership, and Catalent network leadership.

This position will work on complex project controls activities that will require good organization skills, effective meeting leadership and contractor/vendor management, and cross-functional collaboration to drive results across multiple departments. This position will require excellent communication with all levels of the organization. This position is also responsible for detailed project spend tracking and forecasting and project timeline tracking.

The role:

  • Lead development and maintenance of integrated project schedules, resource plans, and cost baselines
  • Lead cross-functional project teams and drive accountability across Engineering, Quality, Validation, and Operations
  • Own project reporting and ensure accurate forecasting of cost and schedule performance
  • Establish and manage capital expenditure (CapEx) requests, including cost tracking and earned value management
  • Drive corrective actions for variances in scope, schedule, and cost performance
  • Partner with Procurement to support sourcing strategy, bid evaluation, and vendor alignment
  • Coordinate and ensure project readiness and turnover to operations, including documentation handoff
  • Interface with internal stakeholders, vendors, contractors, and site/network leadership

The candidate:

  • Bachelor's degree in Construction Management, Chemical, Mechanical, Electrical, Biochemical, or related Engineering discipline
  • Minimum 5+ years of experience leading capital projects from initiation through execution and turnover in a GMP or highly regulated environment
  • Strong experience with project controls, including cost forecasting, schedule management, and earned value management
  • Demonstrated ability to manage project budgets, timelines, and cross-functional teams
  • Experience working with vendors, contractors, and procurement teams on project execution
  • Experience working in a pharmaceutical, biologics, or other regulated manufacturing environment
  • Preferred exposure to bioprocessing systems, clean utilities, and GMP facility design

Why you should join Catalent:

  • Competitive medical benefits and 401K
  • 152 hours PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes

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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