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Project Manager Biotech Jobs in Michigan (NOW HIRING)

Biovire

Manager, Validation

Brighton, MI · On-site

$100K - $120K/yr

... biotechnology, or regulated manufacturing environments * Prior leadership experience within ... Hands-on experience leading validation projects and technical documentation activities * Experience ...

Biovire

Manager, Validation

Brighton, MI · On-site

$100K - $120K/yr

... in pharmaceutical, biotechnology, or regulated manufacturing environmentsPrior leadership ... projects and technical documentation activitiesExperience supporting manufacturing equipment ...

Amgen

Strategic Sourcing Manager

Detroit, MI · On-site

$127K - $165K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project Management Experience - able to lead teams that cut across geographic and functional ...

Hogg Robinson Group

Client Solutions Manager

Three Rivers, MI · On-site

$88K - $163K/yr

... biotech, advertising, entertainment, consulting and other professional services firms. Reporting to ... Strategic thinker with strong problem-solving and multi-project management abilities * Willingness ...

MMS

Nonclinical Writer

Canton, MI · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... Collaborate with cross-functional teams such as project management, safety, efficacy, biostats ...

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... Collaborate with cross-functional teams such as project management, safety, efficacy, biostats ...

Danaher

Senior Director - Operations

Muskegon, MI · On-site

You would be joininga multi-billion-dollar global leader in biotechnology as the SeniorDirector ... Oversee Operational Execution Across Project Workstreams Manage the daily operations of multiple ...

Zifo

GxP Lab Computing Analyst

Wyandotte, MI · On-site

Manage lab computing aspects of installing new, retirement and relocation of equipment * Implement ... Ability to identify, track and complete tasks for multiple projects * Knowledge of laboratory ...

Niowave Inc.

Senior Quality Systems Specialist

Lansing, MI · On-site

$75K - $103K/yr

... biotech environments * Demonstrated experience with the following: * Managing complex quality ... Possesses strong organizational and project management skills for self and teams * Possesses a ...

Zifo

GxP Lab Computing Analyst

Wyandotte, MI · On-site

Manage lab computing aspects of installing new, retirement and relocation of equipment * Implement ... Ability to identify, track and complete tasks for multiple projects * Knowledge of laboratory ...

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All JobsProject Biotech JobsProject Manager Biotech JobsProject Manager Biotech Jobs in Michigan

Project Manager Biotech information

See Michigan salary details

$19

$40

$66

How much do project manager biotech jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for project manager biotech in Michigan is $40.30, according to ZipRecruiter salary data. Most workers in this role earn between $35.00 and $44.23 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 Michigan? For Project Manager Biotech jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Michigan look for? The top searched job categories for Project Manager Biotech jobs in Michigan are:
What cities in Michigan are hiring for Project Manager Biotech jobs? Cities in Michigan with the most Project Manager Biotech job openings:
Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $83,834 per year, or $40.3 per hour.

Manager, Validation

Biovire

Brighton, MI • On-site

$100K - $120K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 27 days ago

Job description

Manager, Validation
Brighton, Michigan
Biovire is advancing toward commercialization with a focus on operational excellence, compliance, and scalable GMP manufacturing systems. We are seeking a Manager, Validation, reporting to the VP, Engineering, to lead validation programs supporting equipment, facilities, utilities, and computerized systems within our regulated pharmaceutical manufacturing environment.
This is a highly visible leadership role responsible for ensuring validation programs support operational readiness, inspection readiness, and long-term manufacturing reliability as the organization continues to scale.
The Role
The Manager, Validation leads commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across the Brighton site. This role provides technical oversight for validation strategy, execution, compliance, and lifecycle management of manufacturing systems and infrastructure.
This position partners closely with Quality, Operations, Manufacturing, Engineering, Maintenance, and cross-functional operational teams to ensure all systems remain compliant, qualified, and inspection-ready.
Key Responsibilities
  • Lead enterprise validation programs supporting equipment, facilities, utilities, automation, and computerized systems across Biovire's GMP manufacturing operations.
  • Oversee commissioning, qualification, and the overall validation strategy and activities.
  • Partner with Operations and Quality to maintain the qualified state of manufacturing systems.
  • Support commercialization, technology transfer, process validation, and startup activities for new manufacturing processes and facilities.
  • Serve as Validation SME during FDA and regulatory inspections.
  • Lead lifecycle management of validation systems.
  • Manage and maintain Validation Master Plans and validation lifecycle documentation
  • Lead scheduling, planning, review, and execution of validation activities
  • Support transition of equipment and systems from Engineering to operational use
  • Partner cross-functionally with Quality, Manufacturing, Engineering, and Maintenance teams
  • Provide technical guidance for risk assessments, change controls, deviations, and investigations
  • Ensure timely completion of validation protocols, reports, traceability matrices, IQ/OQ documentation, and related deliverables
  • Support audit and inspection readiness activities
  • Lead and develop validation personnel while reinforcing a strong quality and compliance culture

What You Bring
  • Bachelor's degree in Engineering, Science, Computer Systems, or related technical field
  • 5+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments
  • Prior leadership experience within Validation, Engineering, CQV, or Quality functions
  • Experience interacting with FDA or other regulatory agencies and supporting inspections.
  • Ability to communicate technical validation concepts during inspections.
  • Strong understanding of cGMP, validation lifecycle management, and 21 CFR Part 11 requirements
  • Hands-on experience leading validation projects and technical documentation activities
  • Experience supporting manufacturing equipment, utilities, HVAC, automation systems, and/or computerized systems
  • Strong organizational, communication, and cross-functional collaboration skills

Why Join Biovire
  • Opportunity to shape and strengthen validation systems during organizational growth
  • High visibility and cross-functional leadership exposure
  • Collaborative and mission-driven GMP manufacturing environment
  • Direct impact supporting operational readiness and future commercialization
  • Company-paid medical, dental, vision, and life insurance
  • Paid Time Off supporting work-life balance

Come join us on our mission of manufacturing safe, high-quality products that improve and save lives.

Apply