Collaborate significantly with cross functional groups including Project Management, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 8 years' experience in related ...
Collaborate significantly with cross functional groups including Project Management, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 8 years' experience in related ...
Collaborate significantly with cross functional groups including Project Management, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 8 years' experience in related ...
Collaborate significantly with cross functional groups including Project Management, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 8 years' experience in related ...
Senior Program Manager - Program Management
Madison, WI · On-site
$116K - $117K/yr
Applies sound project management practices within assigned projects and coaches others in the same ... Professional experience in a related field such as Biologics, Biotechnology, Pharma preferred.
Senior Program Manager - Program Management
Madison, WI · On-site
$116K - $117K/yr
Applies sound project management practices within assigned projects and coaches others in the same ... Professional experience in a related field such as Biologics, Biotechnology, Pharma preferred.
Senior Program Manager - Program Management
Madison, WI · On-site
$116K - $117K/yr
Applies sound project management practices within assigned projects and coaches others in the same ... Professional experience in a related field such as Biologics, Biotechnology, Pharma preferred.
Senior Program Manager - Program Management
Madison, WI · On-site
$116K - $117K/yr
Applies sound project management practices within assigned projects and coaches others in the same ... Professional experience in a related field such as Biologics, Biotechnology, Pharma preferred.
Sr. Product Manager, Custom Media & Strategic Reagents
Madison, WI · On-site
$127K - $168K/yr
Partner closely with commercial teams, PMO, BPG, operations, supply chain, finance, regulatory, and ... life sciences, biotech, pharmaceuticals, health tech, or related industries * Demonstrated ...
Sr. Product Manager, Custom Media & Strategic Reagents
Madison, WI · On-site
$127K - $168K/yr
Partner closely with commercial teams, PMO, BPG, operations, supply chain, finance, regulatory, and ... life sciences, biotech, pharmaceuticals, health tech, or related industries * Demonstrated ...
Partner closely with commercial teams, PMO, BPG, operations, supply chain, finance, regulatory, and ... life sciences, biotech, pharmaceuticals, health tech, or related industries * Demonstrated ...
Partner closely with commercial teams, PMO, BPG, operations, supply chain, finance, regulatory, and ... life sciences, biotech, pharmaceuticals, health tech, or related industries * Demonstrated ...
Manages large research projects for a center or program * Serves as a consultant to project ... Experience in plant biotechnology techniques and workflows * Experience supervising, leading, or ...
Manages large research projects for a center or program * Serves as a consultant to project ... Experience in plant biotechnology techniques and workflows * Experience supervising, leading, or ...
WCIC Business Development Director
Middleton, WI · On-site
$100K/yr
Manages large research projects for a center or program * Serves as a consultant to project ... Experience in plant biotechnology techniques and workflows * Experience supervising, leading, or ...
WCIC Business Development Director
Middleton, WI · On-site
$100K/yr
Manages large research projects for a center or program * Serves as a consultant to project ... Experience in plant biotechnology techniques and workflows * Experience supervising, leading, or ...
Wcic Business Development Director
Middleton, WI · On-site
$100K/yr
Manages large research projects for a center or program * Serves as a consultant to project ... Experience in plant biotechnology techniques and workflows * Experience supervising, leading, or ...
Wcic Business Development Director
Middleton, WI · On-site
$100K/yr
Manages large research projects for a center or program * Serves as a consultant to project ... Experience in plant biotechnology techniques and workflows * Experience supervising, leading, or ...
... projects, change management, and site initiatives. The CandidateMinimum Requirements * Master of Science or Master of Arts in Environmental, Health, Safety & Security, Biochemistry, Biotechnology, or ...
... projects, change management, and site initiatives. The CandidateMinimum Requirements * Master of Science or Master of Arts in Environmental, Health, Safety & Security, Biochemistry, Biotechnology, or ...
Foster cross-functional collaboration across Project Management, Product Development, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 5 years' experience in related ...
Foster cross-functional collaboration across Project Management, Product Development, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 5 years' experience in related ...
Foster cross-functional collaboration across Project Management, Product Development, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 5 years' experience in related ...
Foster cross-functional collaboration across Project Management, Product Development, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 5 years' experience in related ...
Foster cross-functional collaboration across Project Management, Product Development, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 5 years' experience in related ...
Foster cross-functional collaboration across Project Management, Product Development, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 5 years' experience in related ...
Foster cross-functional collaboration across Project Management, Product Development, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 5 years' experience in related ...
Foster cross-functional collaboration across Project Management, Product Development, Manufacturing ... M.S./M.A. in Biotechnology or related field with minimum of 5 years' experience in related ...
Working with project teams to represent Quality Control, conducting risk assessments and ... Advanced level degree preferred * 5+ years of Pharmaceutical or Biotechnology industry experience
Working with project teams to represent Quality Control, conducting risk assessments and ... Advanced level degree preferred * 5+ years of Pharmaceutical or Biotechnology industry experience
Manager, Quality Control
Madison, WI · On-site
Working with project teams to represent Quality Control, conducting risk assessments and ... Advanced level degree preferred * 5+ years of Pharmaceutical or Biotechnology industry experience
Manager, Quality Control
Madison, WI · On-site
Working with project teams to represent Quality Control, conducting risk assessments and ... Advanced level degree preferred * 5+ years of Pharmaceutical or Biotechnology industry experience
Minimum of 5 years of experience managing clinical trials as a Project Manager or in a comparable role at a pharmaceutical/biotech company or CRO. * Minimum of 2 years of supervisory experience with ...
Quick apply
Minimum of 5 years of experience managing clinical trials as a Project Manager or in a comparable role at a pharmaceutical/biotech company or CRO. * Minimum of 2 years of supervisory experience with ...
Minimum of 5 years of experience managing clinical trials as a Project Manager or in a comparable role at a pharmaceutical/biotech company or CRO. * Minimum of 2 years of supervisory experience with ...
Quick apply
Minimum of 5 years of experience managing clinical trials as a Project Manager or in a comparable role at a pharmaceutical/biotech company or CRO. * Minimum of 2 years of supervisory experience with ...
Manager - Environmental, Health, Safety & Security
Madison, WI · On-site
$83K - $113K/yr
... projects, change management, and site initiatives. The Candidate Minimum Requirements * Master of Science or Master of Arts in Environmental, Health, Safety & Security, Biochemistry, Biotechnology ...
Manager - Environmental, Health, Safety & Security
Madison, WI · On-site
$83K - $113K/yr
... projects, change management, and site initiatives. The Candidate Minimum Requirements * Master of Science or Master of Arts in Environmental, Health, Safety & Security, Biochemistry, Biotechnology ...
... biotech, food, or beverage industries is required as well Pay is $50,000 to $70,000 annually, based ... You will join a smaller, collaborative team where you are a key part of the sales and project ...
... biotech, food, or beverage industries is required as well Pay is $50,000 to $70,000 annually, based ... You will join a smaller, collaborative team where you are a key part of the sales and project ...
Project Manager Biotech information
See Madison, WI salary details
$22.05 - $27.04
4% of jobs
$27.04 - $32.04
8% of jobs
$32.04 - $37.04
3% of jobs
$39.23 is the 25th percentile. Wages below this are outliers.
$37.04 - $42.04
21% of jobs
The median wage is $45.17 / hr.
$42.04 - $47.04
21% of jobs
$50.43 is the 75th percentile. Wages above this are outliers.
$47.04 - $52.04
25% of jobs
$52.04 - $57.04
13% of jobs
$57.04 - $62.04
2% of jobs
$62.04 - $67.04
1% of jobs
$67.04 - $72.04
1% of jobs
$72.04 - $77.04
0% of jobs
$22
$46
$77
How much do project manager biotech jobs pay per hour?
What is the difference between Project Manager Biotech vs Clinical Project Manager?
| Aspect | Project Manager Biotech | Clinical Project Manager |
|---|---|---|
| Credentials | Bachelor's or Master's in Life Sciences, Project Management Certification | Bachelor's or Master's in Life Sciences, Clinical Research Certification |
| Work Environment | Biotech companies, R&D labs, manufacturing | Clinical trial sites, hospitals, pharmaceutical companies |
| Industry Usage | Biotech product development, research projects | Clinical trial management, regulatory compliance |
| Common Search/Comparison | Yes | Yes |
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?
What does a Project Manager in Biotech do?
What are the key skills and qualifications needed to thrive as a Project Manager in Biotech, and why are they important?
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 20 days ago
Catalent rating
7.6
Based on 54 frontline employees who took The Breakroom Quiz
50th of 74 rated pharmaceutical
Job description
Manager - Process Development, Downstream
Position Summary:
- Work Schedule: M-F 8am-5pm
- 100% on-site
Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities. This is a unique opening to join a small, fast-growing business, backed by a global public company. People joining our team will have the opportunity for career development as our business continues to grow and expand. Catalent-Madison employees are helping to improve future patient outcomes by working on products that are designed to treat COVID-19, cancer, various autoimmune, fibrotic and blood disorders, HIV, diabetes, heart and lung diseases as well as Alzheimer's.
Catalent Pharma Solutions in Madison, WI is hiring a Manager - Process Development, Downstream.
We are seeking an experienced Downstream Process Development Manager to leadlatestageprocess development and process characterization activities for protein biologics. The ideal candidate brings deep technicalexpertisein downstream unit operations andqualitybydesignprinciples, along withhandsonexperience supportinglatephaseprograms, PPQ readiness, and technology transfer into cGMP manufacturing. This role will provide technical leadership acrosscrossfunctionalteams, ensuring robust process understanding,regulatoryreadydocumentation, and successful execution from clinical through commercial stages.
The Role:
- Supervise assigned team's daily work activities including workload, ensuring training, general guidance to direct reports and across functional groups, and serve as resource for technical/administrative problems
- Hire, train, motivate, lead, develop, and evaluate staff
- Mentor direct reporting people leaders on fundamentals of leadership and career development.
- Take corrective action as necessary on a timely basis and in accordance with company policy
- Ensure compliance with current federal, state, and local regulations. Consult with Human Resources Department as appropriate
- Ensure target timelines to deliver results are met and data integrity
- Interact with customers during meetings as a first line in escalations; provide responses to customer's questions
- Identify and implement new technology/instrumentation for continuous improvement of productivity and throughput
- Author and review technical documents such as Standard Operating Procedures (SOPs), study protocols, and reports
- Communicate effectively and follow detailed written and verbal instruction; ability to clearly communicate and provide mentorship to other groups and clients as necessary
- Ability to provide ideas and introduce new technology for process improvements with the goal of transfer to manufacturing
- Collaborate significantly with cross functional groups including Project Management, Manufacturing, Manufacturing Sciences, and Process Development
- Take responsibility for direct reports' performance by setting clear goals and expectations, tracking
progress against the goals, ensuring constructive feedback, and addressing performance-related concerns and issues promptly - Work with, coach, and support direct reports in developing knowledge, skills, and abilities in the interest of performance improvement and employee's career development
- All other duties as assigned
The Candidate:
- PhD in Biotechnology or related field with minimum of 4 years' experience in related laboratory work/laboratory leadership role; or
- M.S./M.A. in Biotechnology or related field with minimum of 8 years' experience in related laboratory work/laboratory leadership role; or
- B.S./B.A. in Biotechnology or related field with minimum of 10 years' experience in related laboratory work/laboratory leadership role
- Leadership experience minimum 4 years
- Downstream process development andscaleupfor protein biologics, including chromatography, filtration (UF/DF, normal flow), viral clearance, and formulation unit operations
- Leadership experience directing personnel and organizational group management, including mentoring and training staff members cross-functionally
- Experience in applying GMP/GDP in compliance with international regulatory expectations and requirements is a plus
- Process characterization and validation support, including identification of CPPs, CQAs, and establishment of control strategies aligned withQbDprinciples
- Latephaseand PPQ readiness support, including authoring or reviewing development reports, characterization protocols, validation strategies, andregulatorysupportingdocumentation
- Technology transfer to cGMP manufacturing, includingscaledownmodel definition, risk assessments, and troubleshooting during manufacturing execution
- Strong working knowledge of cGMP expectations, data integrity, and good documentation practices for biologics manufacturing
- Application of statistical and experimental design tools (e.g., DoE) to support process robustness, lifecycle management, and comparability assessments
- Crossfunctionalleadership working with MS&T, Manufacturing, Quality, and Analytical Development to drive aligned technical and execution strategies
- People and technical leadership experience, including mentoring scientists and managing execution across multiple complex programs
- Experience interacting and liaising with internal and external clients, customers, and/or suppliersrequired
- Experience managing continuous improvement initiatives, lean principles, and 5S is preferred
Why you should join Catalent:
- Defined career path and annual performance review and feedback process
- Diverse, inclusive culture
- Positive working environment focusing on continually improving processes to remain innovative
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
- 152 hours of PTO + 8 paid holidays
- Generous 401K match
- Medical, dental and vision benefits effective day one of employment
- Tuition Reimbursement- Let us help you finish your degree or start a new degree!
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