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Cmc Project Manager Jobs in Michigan (NOW HIRING)

MMS

Nonclinical Writer

Canton, MI · On-site

Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC * Demonstrated ability to lead others to complete complex projects

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC * Demonstrated ability to lead others to complete complex projects

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All JobsCmc Project JobsCmc Project Manager JobsCmc Project Manager Jobs in Michigan

Cmc Project Manager information

See Michigan salary details

$39.2K

$91.5K

$147.7K

How much do cmc project manager jobs pay per year?

As of Jul 13, 2026, the average yearly pay for cmc project manager in Michigan is $91,540.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,300.00 and $112,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Cmc Project Manager position, and why are they important?

A CMC Project Manager needs strong expertise in Chemistry, Manufacturing, and Controls (CMC) processes, project management certifications (such as PMP), and a background in pharmaceutical or biotech industries. Familiarity with regulatory submission systems, quality management software, and documentation tools is highly valued. Exceptional organizational skills, problem-solving ability, and effective cross-functional communication help candidates excel in this role. These capabilities are critical for ensuring project milestones are met, regulatory requirements are satisfied, and product development remains on track.

What are some typical responsibilities of a CMC Project Manager in a pharmaceutical company?

A CMC Project Manager is responsible for coordinating cross-functional teams to ensure successful delivery of project milestones related to product development, manufacturing, and regulatory submissions. Their daily tasks often include developing project timelines, managing risk assessments, overseeing documentation, and facilitating communication between technical, regulatory, and quality departments. They play a pivotal role in preparing CMC sections for regulatory filings, supporting process optimization, and troubleshooting manufacturing challenges. This position requires excellent multitasking abilities and close collaboration with internal stakeholders and external partners throughout the product lifecycle.

What is a CMC Project Manager job?

A CMC (Chemistry, Manufacturing, and Controls) Project Manager oversees the development, manufacturing, and regulatory aspects of pharmaceutical products. They coordinate cross-functional teams, manage timelines, and ensure compliance with regulatory requirements. Their role is critical in guiding drug development from early stages to commercialization while maintaining quality and efficiency.

What are popular job titles related to Cmc Project Manager jobs in Michigan? For Cmc Project Manager jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Cmc Project Manager jobs in Michigan look for? The top searched job categories for Cmc Project Manager jobs in Michigan are:
Cmc Project Manager jobs near you
Infographic showing various Cmc Project Manager job openings in Michigan as of July 2026, with employment types broken down into 20% Internship, 1% As Needed, 63% Full Time, 11% Part Time, 3% Contract, and 2% Summer. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $91,540 per year, or $44 per hour.
Project Manager

Project Manager

Grand River Aseptic Manufacturing

Grand Rapids, MI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 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, as well as managing ongoing Commercial Supply and Life Cycle Management (LCM) projects. This role serves as the primary liaison between customers and cross-functional internal teams, overseeing 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. The Project Manager is responsible for authoring project work orders/change orders, and other project documentation while maintaining accurate and up to date project data in SmartSheet. The role requires strong organizational, communication, and relationship-management skills. 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, Biomedical Engineering or other Life Sciences or related field, and a minimum of 4 years related work experience in Pharma/Biotech/Life Sciences or similarly regulated industry.
  • Proficient in project management software required.
  • Training or education in project management or equivalent knowledge and experience.
  • Knowledge of project management techniques and tools.
  • Experience in a pharmaceutical manufacturing, laboratory, or CMC regulatory environment.
  • Regulatory knowledge of pharmaceutical manufacturing with GMPs, change control, risk management and quality by design.

Preferred Requirements:
  • Direct work experience in project management capacity, specifically with tech transfer of products into a sterile manufacturing facility.
  • Customer facing experience in pharmaceutical environment.
  • 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.
  • Build strong client relationships, manage expectations, and improve customer satisfaction.
  • Support customer visits and maintain flexibility in a dynamic environment.
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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