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Biotechnology Project Manager 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 ...

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 JobsBiotechnology Project JobsBiotechnology Project Manager JobsBiotechnology Project Manager Jobs in Michigan

Biotechnology Project Manager information

See Michigan salary details

$19

$40

$66

How much do biotechnology project manager jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for biotechnology project manager 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 does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.
What are popular job titles related to Biotechnology Project Manager jobs in Michigan? For Biotechnology Project Manager jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Biotechnology Project Manager jobs in Michigan look for? The top searched job categories for Biotechnology Project Manager jobs in Michigan are:
What cities in Michigan are hiring for Biotechnology Project Manager jobs? Cities in Michigan with the most Biotechnology Project Manager job openings:
Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Michigan 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 $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 25 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