1

Project Manager Biotech Jobs in Michigan (NOW HIRING)

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 ...

Patient Services Technical Manager

Detroit, MI · On-site

$114K - $115K/yr

Leveraging your expertise in patient services, you will interface between pharmaceutical, biotech ... You will design, implement and optimize patient support programs, define project roadmaps and ...

Manager of Sterility Assurance

Brighton, MI · On-site

$107K - $129K/yr

... projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to ... the biotech / pharmaceutical industry, with 2+ years in Sterility Assurance / Environmental ...

Manager of Sterility Assurance

Brighton, MI · On-site

$107K - $129K/yr

... projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to ... the biotech / pharmaceutical industry, with 2+ years in Sterility Assurance / Environmental ...

Manager of Sterility Assurance

Brighton, MI · On-site

$107K - $129K/yr

... projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to ... the biotech / pharmaceutical industry, with 2+ years in Sterility Assurance / Environmental ...

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 ...

Lead accounting for capital projects, including grants, incentives, fixed assets, depreciation, and ... Experience in biotech, pharmaceutical, healthcare, or other regulated environments preferred

Lead accounting for capital projects, including grants, incentives, fixed assets, depreciation, and ... Experience in biotech, pharmaceutical, healthcare, or other regulated environments preferred

... biotechnology, or regulated manufacturing environments * Prior leadership experience within ... management, and 21 CFR Part 11 requirements * Hands-on experience leading validation projects and ...

next page

Showing results 1-20

Project Manager Biotech information

See Michigan salary details

$19

$40

$66

How much do project manager biotech jobs pay per hour?

As of Jun 26, 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, and why are they important?

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:
QA Specialist I/II - Technical Support

QA Specialist I/II - Technical Support

Grand River Aseptic Manufacturing, Inc.

Grand Rapids, MI

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago


Job description

Description

Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day!


Overview of this Position:

Provides quality support to both internal and external projects, including the on-boarding of new clients / client projects, capital expenditures (CAPEX), continuous improvement initiatives, and as required in routine manufacturing and finishing operations. This position works closely with Project Managers, Filling and Finishing Operations, Quality Assurance Operations, Analytical Technical Services, Manufacturing Science & Technology, Validation, and QC Analytical and Microbiology departments. This is not a remote role. 


Non-Negotiable Requirements:

  • Completion of a bachelor's degree in Life Sciences or a related field and/or a minimum of 1-3 years of related work experience for a Specialist I, 3-5 years for a Specialist II, 5-7 for a Specialist III, and 7+ years for a Sr. Specialist. 
  • Experience and expertise of QA principles and procedures in pharma, biopharma, and/or biotech manufacturing environment or manufacturing environment of regulated products with a thorough understanding of cGMP, FDA guidelines and multinational regulatory standards. 
  • Proficient computer skills in Microsoft Word, Excel, and Outlook. 

Preferred Requirements:

  • QA Experience and expertise in aseptic environment.

Responsibilities Include (but are not limited to):

  • Provide working knowledge of GMP and regulatory requirements as it relates to performing Quality Assurance review and approval of cGMP documentation in support of GRAM and client-driven projects including: 
  • Standard Operating Procedures
  • Test Methods
  • Raw Material, Component, and Finished Product Specifications
  • Risk Assessments including change control assessments
  • Master Batch Records
  • Validation Documents
  • Provide review of executed batch records in relation to initial technical transfer and process performance qualifications. 
  • Support current clients and on-boarding of new client projects. 
  • Manage Quality deliverables according to project schedules and ensure tasks assigned are delivered according to project timeline.
  • Ensure that project deliverables meet all regulatory and industry best practice standards.
  • QA representative on project teams to ensure that project deliverables meet all regulatory and industry best practice standards as well as internal deadlines. 
  • Participate in deviation investigation teams to support quality investigations (NCR, LIR, SQIR, etc.). 

Full job description available during formal interview process.


What Sets GRAM Apart from Other Employers:

BENEFITS starting day 1: Medical, prescription, dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying a portion of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!

Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!

PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!

WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose. 

PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!

PAY: Depends on Experience and is discussed during the interview process.

If you meet the required criteria listed above, GRAM welcomes you to apply today!