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Process Development Manager Jobs in Canton, MI (NOW HIRING)

Biovire

Process Development Manager

Brighton, MI · On-site

Manager, Process Development Engineering Organization Brighton, Michigan Biovire is advancing toward commercialization with a focus on innovation, operational excellence, and scalable GMP ...

Biovire

Manager, Process Development

Brighton, MI

Manager, Process Development Engineering Organization Brighton, Michigan Biovire is advancing toward commercialization with a focus on innovation, operational excellence, and scalable GMP ...

Biovire

Manager, Process Development

Brighton, MI · On-site

$100K - $120K/yr

We are seeking a Manager, Process Development to lead technical transfer activities for sterile injectable pharmaceutical and medical device products while driving process robustness, manufacturing ...

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Process Development Manager information

See Canton, MI salary details

$69.5K

$89.4K

$158.9K

How much do process development manager jobs pay per year?

As of Aug 10, 2026, the average yearly pay for process development manager in Canton, MI is $89,376.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,100.00 and $89,400.00 per year, depending on experience, location, and employer.

What does a process development manager do?

A process development manager oversees the design, implementation, and optimization of manufacturing or operational processes to improve efficiency, quality, and cost-effectiveness. They analyze workflows, collaborate with cross-functional teams, and often utilize tools like Six Sigma or Lean methodologies to develop scalable processes. Strong project management and problem-solving skills are essential in this role.

What are some common challenges faced by a process development manager, and how can they be addressed?

Process Development Managers often encounter challenges such as aligning cross-functional teams, managing resource constraints, and adapting processes to evolving business needs. Effective communication and collaboration with stakeholders in production, quality, and R&D are essential to overcome these obstacles. Proactively identifying potential bottlenecks, staying updated with industry best practices, and fostering a culture of continuous improvement can help ensure smoother process development and implementation.

What is the difference between Process Development Manager vs Process Engineer?

AspectProcess Development ManagerProcess Engineer
ResponsibilitiesOversees process improvement projects, manages teams, develops strategies for scalable processesDesigns, tests, and implements specific manufacturing processes, focuses on technical execution
Required CredentialsBachelor's or Master's in Engineering, experience in process management, certifications like Six SigmaBachelor's in Engineering or related field, technical skills, certifications like Lean or Six Sigma
Work EnvironmentLeadership roles in manufacturing or R&D settings, cross-functional collaborationHands-on technical work in manufacturing or laboratory settings
Industry UsageCommon in manufacturing, pharmaceuticals, biotech industriesWidely used in manufacturing, chemical, and industrial sectors

The Process Development Manager focuses on strategic oversight and team leadership for process improvements, while the Process Engineer handles technical process design and implementation. Both roles require similar credentials and are integral to manufacturing industries, but differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a process development manager?

To thrive as a Process Development Manager, you need a solid background in process engineering, project management, and analytical problem-solving, typically supported by a degree in engineering, chemistry, or a related field. Familiarity with process simulation software, Lean Six Sigma methodologies, and quality management systems like ISO standards is commonly required. Strong leadership, communication, and change management skills help drive cross-functional collaboration and successful project implementation. These competencies are crucial for optimizing processes, ensuring product quality, and achieving operational efficiency in a competitive business environment.
What job categories do people searching Process Development Manager jobs in Canton, MI look for? The top searched job categories for Process Development Manager jobs in Canton, MI are:
What cities near Canton, MI are hiring for Process Development Manager jobs? Cities near Canton, MI with the most Process Development Manager job openings:
Process Development Manager jobs near you
Infographic showing various Process Development Manager job openings in Canton, MI as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $89,376 per year, or $43 per hour.

Process Development Manager

Biovire

Brighton, MI • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Posted 14 days ago

Job description

Manager, Process Development
Engineering Organization
Brighton, Michigan
Biovire is advancing toward commercialization with a focus on innovation, operational excellence, and scalable GMP manufacturing. We are seeking a Manager, Process Development to lead technical transfer activities for sterile injectable pharmaceutical and medical device products while driving process robustness, manufacturing readiness, and continuous improvement across our Brighton manufacturing facility.
This is a highly visible leadership role responsible for leading Process Development activities that support new product introductions, technology transfer, process optimization, and successful commercialization while partnering closely with Manufacturing, Quality, Validation, Engineering, and other cross-functional teams.
The Role
Reporting to the Director, Pharmaceutical Technologies, the Manager, Process Development, provides technical and people leadership for product transfer and process development activities that support sterile injectable pharmaceutical and medical device manufacturing.
This role leads a team of Process Engineers and ensures that manufacturing processes are technically sound, scalable, compliant, and capable of consistently producing high-quality products. The position partners closely with Manufacturing, Quality, Validation, Engineering, Supply Chain, and other cross-functional stakeholders to support successful product launches, operational readiness, and continuous process improvement.
Key Responsibilities
  • Lead technical transfer activities for sterile injectable pharmaceutical and medical device products from development through commercial manufacturing.
  • Manage and develop a team of Process Engineers while fostering a collaborative, high-performing culture.
  • Partner with Manufacturing to support production schedules and ensure successful execution of product transfer activities.
  • Drive process optimization, continuous improvement, and implementation of manufacturing best practices.
  • Ensure compliance with current Good Manufacturing Practices (cGMP), company policies, quality standards, and regulatory requirements.
  • Develop, review, and maintain Master Batch Records, Standard Operating Procedures (SOPs), validation master plans, cleaning validation documentation, containment strategies, and technical transfer documentation.
  • Utilize manufacturing expertise to identify opportunities for process improvements that enhance product quality, efficiency, and operational reliability.
  • Collaborate cross-functionally with Manufacturing, Quality, Validation, Engineering, and other operational teams to ensure successful product transfers and commercialization.
  • Support manufacturing investigations, technical problem-solving, and implementation of corrective and preventive actions as appropriate.
  • Lead training, coaching, and development of Process Engineers while promoting accountability, technical excellence, and continuous learning.
  • Promote a safe working environment and reinforce Biovire's commitment to quality, compliance, and operational excellence.

What You Bring
  • Bachelor's degree in Biology, Chemistry, Chemical Engineering, Biomedical Engineering, or another related life science or technical discipline required.
  • Graduate degree in Chemistry, Biochemistry, Molecular Biology, Chemical Engineering, Biomedical Engineering, or a related life science preferred.
  • Minimum 5 years of pharmaceutical industry experience.
  • 2-5 years of leadership or people management experience preferred.
  • Demonstrated experience supporting process development, technical transfer, or pharmaceutical manufacturing operations.
  • Strong understanding of cGMP requirements, pharmaceutical manufacturing processes, and regulatory expectations.
  • Experience developing or maintaining manufacturing documentation including Master Batch Records, SOPs, validation documentation, and technical transfer packages.
  • Excellent organizational, communication, technical writing, and cross-functional collaboration skills.
  • Proven ability to lead teams, prioritize multiple projects, and drive continuous improvement initiatives.
  • Demonstrated commitment to safety, quality, integrity, and operational excellence.

Why Join Biovire
  • Opportunity to lead technical transfer and process development activities supporting commercialization of innovative therapies.
  • High visibility and cross-functional leadership exposure across Manufacturing, Engineering, Quality, Validation, and Pharmaceutical Technologies.
  • Collaborative and mission-driven GMP manufacturing environment.
  • Direct impact on new product introductions, manufacturing readiness, and continuous improvement initiatives.
  • Company-sponsored medical, dental, vision, and life insurance.
  • Paid Time Off supporting work-life balance.
  • Opportunity to build and develop a growing Process Development team.

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

Apply