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Biotechnology Project Manager Jobs in Michigan (NOW HIRING)

Premier Research

$122K/yr

Premier Research is looking for a Senior Project Manager, Dermatology to join our General Medicine ... You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and ...

GenScript/ProBio

$60 - $80/hr

About GenScript Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation ... Construction Project Manager - Facility Renovation & Fit-Out Location: Piscataway, NJ (Fully onsite ...

Danaher

Senior IT Portfolio & Governance Lead

Detroit, MI · On-site +1

$129K - $130K/yr

... biotechnology? AtCepheid,one ofDanaher's15+ operating companies, our work saves lives-and we're all ... The position partners with project managers, resource managers, and business stakeholders to ...

University of Michigan

Program Manager

Ann Arbor, MI · On-site

... connecting life science, biotechnology, pharmaceutical, medical device, and digital health ... Success in this role requires exceptional project management, organizational, communication, and ...

Stark Pharma Solutions Inc

Technician

Portage, MI · On-site

... Project Management, and IT, with a focus on delivering tailored solutions that drive growth ... biotech, medical device, or regulated manufacturing. * Experience operating or supporting ...

Legend Biotech US

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Managing the prosecution of active global dockets, including handling U.S. and foreign patent ...

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Biotechnology Project Manager information

See Michigan salary details

$19

$40

$66

How much do biotechnology project manager jobs pay per hour?

As of Sep 8, 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 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 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 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 82% Full Time, 13% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $83,834 per year, or $40.3 per hour.

Project Manager

Grand Rapids, MI • On-site

Grand River Aseptic Manufacturing
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Grand River Aseptic Manufacturingexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Job description

Project Manager
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:
The Project Manager is responsible for leading technology transfer projects for new products being introduced into GRAM manufacturing facilities and/or manage ongoing Commercial Supply and Life Cycle Management (LCM) projects. Serves as the primary liaison between customers and cross-functional internal teams, oversees all phases of project execution from initiation through closure. Key responsibilities include developing and maintaining project schedules, defining scope, tracking milestones, managing risks, assigning responsibilities and action items, monitoring critical path activities, and ensuring timely resolution or escalation of issues. Responsible for authoring project work orders/change orders, and other project documentation while maintaining accurate and up to date project data in SmartSheet. Strong organizational, communication, and relationship-management skills required.
This is a fully onsite position requiring flexibility to support customer visits and a dynamic project environment.
Non-Negotiable Requirements:
  • Bachelor's degree in Project Management, Biochemistry, or other Life Sciences or related field
  • 4 years related work experience in Pharma/Biotech/Life Sciences or similarly regulated industry.
  • Must have proficient computer skills in Microsoft Word, Excel, SharePoint, Outlook PowerPoint, and other relevant Project Management software (i.e. SmartSheet).
  • Experience in a pharmaceutical manufacturing, laboratory, or CMC regulatory environment.
  • Proficient in project management software required
  • Training or education in project management or equivalent knowledge and experience.
  • Regulatory knowledge of pharmaceutical manufacturing with GMPs, change control, risk management and quality by design.
  • Direct work experience in project management capacity, specifically with tech transfer of products into a sterile manufacturing facility.
  • Customer facing experience in pharmaceutical environment.

Preferred Requirements:
  • PMP Certification desired.

Responsibilities Include (but are not limited to):
  • Lead end-to-end project management for technology transfer, commercial supply, and lifecycle management (LCM) projects.
  • Serve as the primary liaison between customers and cross-functional internal teams.
  • Define project scope, milestones, deliverables, timelines, risks, and success criteria.
  • Manage change controls, tech transfer plans, and project documentation.
  • Oversee execution of commercial supply agreements and ensure contractual commitments are met.
  • Coordinate resources and deliverables across multiple departments.
  • Facilitate project meetings, agendas, action items, and meeting minutes.
  • Drive risk identification, mitigation planning, issue resolution, and escalation.
  • Provide regular project updates to customers and senior leadership.
  • Identify, resolve and/or escalate issues in a timely fashion.
  • Build strong client relationships, manage expectations, and improve customer satisfaction.
  • Support customer visits and maintain flexibility in a dynamic environment.
  • Seek opportunities to increase client satisfaction and deepen relationships.
  • Assists with the professional development of the Project Managers and Associate Project Managers.
  • Identify opportunities for improvement and make constructive suggestions for change.
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!
PAID TIME OFF: You choose how to use this time for your vacation, sick, or mental health needs! PTO: Full-time employees accrue up to 104 hours of paid time off per calendar year, with this amount being prorated your first year. WELLNESS TIME OFF (WTO): In addition to PTO, employees earn 1 hour of wellness 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!

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