Process Development Manager
Brighton, MI · On-site
The position partners closely with Manufacturing, Quality, Validation, Engineering, Supply Chain ... plans, cleaning validation documentation, containment strategies, and technical transfer ...
Process Development Manager
Brighton, MI · On-site
The position partners closely with Manufacturing, Quality, Validation, Engineering, Supply Chain ... plans, cleaning validation documentation, containment strategies, and technical transfer ...
Manager, Process Development
Brighton, MI · On-site
$100K - $120K/yr
The position partners closely with Manufacturing, Quality, Validation, Engineering, Supply Chain ... plans, cleaning validation documentation, containment strategies, and technical transfer ...
Quick apply
Manager, Process Development
Brighton, MI · On-site
$100K - $120K/yr
The position partners closely with Manufacturing, Quality, Validation, Engineering, Supply Chain ... plans, cleaning validation documentation, containment strategies, and technical transfer ...
Support cleaning validation and cleaning verification analysis for GMP manufacturing areas ... engineers and related professionals in discovery and development of novel therapies, keeping ...
Support cleaning validation and cleaning verification analysis for GMP manufacturing areas ... engineers and related professionals in discovery and development of novel therapies, keeping ...
... closely with engineers, operators, and other team members to minimize downtime and support ... Carry out preventive maintenance tasks, including cleaning, lubrication, adjustments, and parts ...
... closely with engineers, operators, and other team members to minimize downtime and support ... Carry out preventive maintenance tasks, including cleaning, lubrication, adjustments, and parts ...
Manages personnel, budgets and projects relating to systems, process, cleaning and equipment ... Supports Product and Engineering Departments in the selection, review, acquisition, and upgrade of ...
Manages personnel, budgets and projects relating to systems, process, cleaning and equipment ... Supports Product and Engineering Departments in the selection, review, acquisition, and upgrade of ...
Reporting to the Service Engineering Manager, this role will solely be responsible for on-vehicle ... Must have a valid driver's license with a clean driving record. WHAT YOU GET TO DO * Create repair ...
Reporting to the Service Engineering Manager, this role will solely be responsible for on-vehicle ... Must have a valid driver's license with a clean driving record. WHAT YOU GET TO DO * Create repair ...
Reporting to the Service Engineering Manager, this role will solely be responsible for on-vehicle ... Must have a valid driver's license with a clean driving record. WHAT YOU GET TO DO * Create repair ...
Reporting to the Service Engineering Manager, this role will solely be responsible for on-vehicle ... Must have a valid driver's license with a clean driving record. WHAT YOU GET TO DO * Create repair ...
Execute comprehensive validation test plans for machinery, ensuring compliance with engineering ... Valid driver's license and a clean driving record. * Ability to obtain and hold a US passport.
Execute comprehensive validation test plans for machinery, ensuring compliance with engineering ... Valid driver's license and a clean driving record. * Ability to obtain and hold a US passport.
Execute comprehensive validation test plans for machinery, ensuring compliance with engineering ... Valid driver's license and a clean driving record. * Ability to obtain and hold a US passport.
Execute comprehensive validation test plans for machinery, ensuring compliance with engineering ... Valid driver's license and a clean driving record. * Ability to obtain and hold a US passport.
Engineer Sr - EMC Test
Auburn Hills, MI · On-site
Making automotive technology that is smarter, cleaner, safer and lighter. That's what we're ... Generate and maintain all necessary validation engineering documentation and data to ensure ...
Engineer Sr - EMC Test
Auburn Hills, MI · On-site
Making automotive technology that is smarter, cleaner, safer and lighter. That's what we're ... Generate and maintain all necessary validation engineering documentation and data to ensure ...
Engineer Sr - EMC Test
Auburn Hills, MI · On-site
Making automotive technology that is smarter, cleaner, safer and lighter. That's what we're ... Generate and maintain all necessary validation engineering documentation and data to ensure ...
Engineer Sr - EMC Test
Auburn Hills, MI · On-site
Making automotive technology that is smarter, cleaner, safer and lighter. That's what we're ... Generate and maintain all necessary validation engineering documentation and data to ensure ...
Design Release Engineer (Air intake Systems)
Auburn Hills, MI · Hybrid
$30 - $32/hr
Depending on program assignments, engineer may be required to support sourcing activities and/or ... A valid driver's license is required as well as a clean driving record. Will be required to drive a ...
Quick apply
Design Release Engineer (Air intake Systems)
Auburn Hills, MI · Hybrid
$30 - $32/hr
Depending on program assignments, engineer may be required to support sourcing activities and/or ... A valid driver's license is required as well as a clean driving record. Will be required to drive a ...
Design Release Engineer (Air intake Systems)
Auburn Hills, MI · On-site
$90 - $120/hr
InDepth Engineering Solutions, LLC | Contract Design Release Engineer (Air intake Systems) Auburn ... A valid driver's license is required as well as a clean driving record. Will be required to drive a ...
Design Release Engineer (Air intake Systems)
Auburn Hills, MI · On-site
$90 - $120/hr
InDepth Engineering Solutions, LLC | Contract Design Release Engineer (Air intake Systems) Auburn ... A valid driver's license is required as well as a clean driving record. Will be required to drive a ...
This role focuses on creating, cleaning, and preparing high-quality CAD geometry for simulation and ... Support powertrain development projects from concept through to validation. Required Qualifications:
This role focuses on creating, cleaning, and preparing high-quality CAD geometry for simulation and ... Support powertrain development projects from concept through to validation. Required Qualifications:
May be required to drive a company vehicle; a valid driver's license and clean driving record are ... MS degree in Engineering. * Minimum of 2 years of CAE experience. * Extensive hands-on experience ...
May be required to drive a company vehicle; a valid driver's license and clean driving record are ... MS degree in Engineering. * Minimum of 2 years of CAE experience. * Extensive hands-on experience ...
\n \n \n Test Planning Engineer\n \n \n * Responsible for developing a full\-vehicle DVP&R and ... Valid driver's license is required as well as a clean driving record. \n \n \n \n
\n \n \n Test Planning Engineer\n \n \n * Responsible for developing a full\-vehicle DVP&R and ... Valid driver's license is required as well as a clean driving record. \n \n \n \n
CAE Engineer
Livonia, MI · On-site
Prepare and clean CAD geometry for CAE model development and analysis. * Develop finite element ... Support planning and execution of hardware testing activities required for model validation and ...
New
CAE Engineer
Livonia, MI · On-site
Prepare and clean CAD geometry for CAE model development and analysis. * Develop finite element ... Support planning and execution of hardware testing activities required for model validation and ...
New
Control Tower Engineer
$57 - $59/hr
... validate clean points, and identify responsible functional areas Develop and recommend triage ... engineering, supplier quality, manufacturing, and service teams Analyze components and vehicle ...
Control Tower Engineer
$57 - $59/hr
... validate clean points, and identify responsible functional areas Develop and recommend triage ... engineering, supplier quality, manufacturing, and service teams Analyze components and vehicle ...
Staff Engineer
Auburn Hills, MI · Hybrid
Advancing sustainability today, powering a cleaner tomorrow. PHINIA is an independent, market ... Oversee engineering analysis efforts for mechanical simulation & digital validation of Canister and ...
Staff Engineer
Auburn Hills, MI · Hybrid
Advancing sustainability today, powering a cleaner tomorrow. PHINIA is an independent, market ... Oversee engineering analysis efforts for mechanical simulation & digital validation of Canister and ...
Staff Engineer
Auburn Hills, MI · On-site
Advancing sustainability today, powering a cleaner tomorrow. PHINIA is an independent, market ... Oversee engineering analysis efforts for mechanical simulation & digital validation of Canister and ...
Staff Engineer
Auburn Hills, MI · On-site
Advancing sustainability today, powering a cleaner tomorrow. PHINIA is an independent, market ... Oversee engineering analysis efforts for mechanical simulation & digital validation of Canister and ...
Cleaning Validation Engineer information
See Michigan salary details
$19.69 - $24.09
2% of jobs
$24.09 - $28.49
6% of jobs
$28.49 - $32.89
13% of jobs
$34.27 is the 25th percentile. Wages below this are outliers.
$32.89 - $37.29
13% of jobs
$37.29 - $41.69
11% of jobs
The median wage is $43.89 / hr.
$41.69 - $46.09
12% of jobs
$46.09 - $50.49
9% of jobs
$53.89 is the 75th percentile. Wages above this are outliers.
$50.49 - $54.89
13% of jobs
$54.89 - $59.29
13% of jobs
$59.29 - $63.69
6% of jobs
$63.69 - $68.09
3% of jobs
$19
$45
$68
How much do cleaning validation engineer jobs pay per hour?
As of Aug 7, 2026, the average hourly pay for cleaning validation engineer in Michigan is $45.32, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $55.10 per hour, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as a cleaning validation engineer, and why are they important?
To thrive as a Cleaning Validation Engineer, you need a strong background in chemical engineering, microbiology, or a related field, often complemented by experience in GMP-regulated industries. Familiarity with validation protocols, analytical testing methods, and documentation tools (such as LIMS or QMS software) is essential, and certifications like Six Sigma or ASQ may be advantageous. Strong attention to detail, analytical thinking, and effective communication are key soft skills for success in the role. These capabilities are crucial to ensure regulatory compliance, product safety, and effective cross-functional collaboration in pharmaceutical or biotech manufacturing environments.
What is a cleaning validation engineer?
A Cleaning Validation Engineer ensures that manufacturing equipment and processes meet regulatory standards for cleanliness in industries like pharmaceuticals, biotech, and medical devices. They develop validation protocols, conduct tests, analyze data, and document results to confirm that cleaning procedures effectively remove contaminants. This role involves collaborating with quality assurance, production, and regulatory teams to maintain compliance with FDA, GMP, and other industry regulations.
What are the main challenges faced by cleaning validation engineers in the pharmaceutical industry?
Cleaning Validation Engineers in the pharmaceutical industry often face challenges such as staying up-to-date with evolving regulatory requirements, troubleshooting complex cleaning failures, and thoroughly documenting all validation activities. Balancing the needs for robust contamination control with operational efficiency requires analytical thinking and strong problem-solving abilities. Collaboration with manufacturing, quality assurance, and laboratory teams is frequent, as cleaning validation projects require input and support from multiple departments. Successfully managing these challenges ensures product safety, regulatory compliance, and continuous process improvement within manufacturing operations.
What are popular job titles related to Cleaning Validation Engineer jobs in Michigan? For Cleaning Validation Engineer jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Cleaning Validation Engineer jobs in Michigan look for? The top searched job categories for Cleaning Validation Engineer jobs in Michigan are:
Full-time
Medical, Dental, Vision, Life, PTO
Posted 11 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
What You Bring
Why Join Biovire
Come join us on our mission of manufacturing safe, high-quality products that improve and save lives.
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.