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Pharmaceutical Quality Engineer Jobs in Michigan

Experience in the medical device, pharmaceutical, biotechnology, or other regulated manufacturing industry. * ASQ Certified Quality Engineer (CQE), Certified Reliability Engineer (CRE), Certified Six ...

Quality Engineer

Clinton, MI · On-site

$71K - $91K/yr

Quality Engineer Company: Omega Plastics Inc Primary Location: 24401 Capital Blvd, Clinton Township ... pharmaceutical and surgical markets. The company serves key industries, including medical ...

Quality Engineer

Clinton Township, MI · On-site

$66K - $86K/yr

Acts as the primary advocate for compliance and Quality Assurance Engineering of medical devices ... pharmaceutical and surgical markets. The company serves key industries, including medical ...

Sr Quality Engineer

Walker, MI · On-site

$85K - $115K/yr

Job Summary Provide engineering support on duties such as inspection, processing and managing non-conforming materials (NCMRs), supporting production with quality issues and production process audits ...

Sr Quality Engineer

Walker, MI · On-site

$85K - $115K/yr

Job Summary Provide engineering support on duties such as inspection, processing and managing non-conforming materials (NCMRs), supporting production with quality issues and production process audits ...

Process Quality Engineering * Manage quality performance throughout the manufacturing process and ... Experience with manufacturing processes in battery, chemical, pharmaceutical, or other process ...

Projects will focus on improvements to safety, yields, quality, cost effectiveness, and throughput ... Instruct and train West Pharmaceutical Services personnel in the use of any special equipment that ...

Technician, Quality

Walker, MI · On-site

$17.25 - $23.25/hr

... Engineering Change Requests (ECR's). * Assist in the design & drawing reviews and make ... Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its ...

Chemical Process Engineer

Ada, MI · On-site

$92K - $113K/yr

... Quality Engineering or a related technical role. * Experience with nutrition, food, pharmaceutical, consumer packaged goods, or other regulated manufacturing industries. Skills to be successful in ...

Chemical Process Engineer

Ada, MI · On-site

$92K - $113K/yr

... Quality Engineering or a related technical role. * Experience with nutrition, food, pharmaceutical, consumer packaged goods, or other regulated manufacturing industries. Skills to be successful in ...

Bachelor's degree in Life Sciences (biology, chemistry, biochemistry, Engineering (chemical, biomedical, industrial), or related field * 10+ years of GMP/Quality experience in pharmaceutical or ...

Quality Technician

Lansing, MI

$16.50 - $22/hr

We are a group of scientists, engineers, designers, technicians, and many others who are dedicated ... role in the pharmaceutical or medical device industry. * Experience with Minitab, JMP, or ...

Pharmacist

Troy, MI

$60 - $63/hr

Maintain productivity and quality standards within a fast-paced verification environment ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

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Showing results 1-20

Pharmaceutical Quality Engineer information

See Michigan salary details

$39.2K

$73.2K

$103.7K

How much do pharmaceutical quality engineer jobs pay per year?

As of Sep 8, 2026, the average yearly pay for pharmaceutical quality engineer in Michigan is $73,248.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,800.00 and $81,100.00 per year, depending on experience, location, and employer.

What is a pharmaceutical quality engineer?

A Pharmaceutical Quality Engineer ensures that pharmaceutical manufacturing processes, products, and systems comply with regulatory standards and quality requirements. They develop and implement quality control procedures, conduct audits, and troubleshoot production issues to maintain compliance. Their role involves working closely with cross-functional teams to improve product quality and efficiency. They also analyze data, oversee validation processes, and ensure adherence to Good Manufacturing Practices (GMP).

What are the daily responsibilities of a pharmaceutical quality engineer?

Pharmaceutical Quality Engineers typically spend their days performing process validations, analyzing production data, and conducting root cause investigations of quality issues. They collaborate closely with manufacturing, laboratory, and regulatory teams to ensure products comply with internal standards and external regulations. The role often involves writing and reviewing documentation, supporting audits, and recommending improvements to manufacturing processes. This position blends hands-on problem-solving with cross-functional communication, making it both dynamic and impactful on the overall quality and safety of pharmaceutical products.

What skills and qualifications are needed to be a pharmaceutical quality engineer?

To thrive as a Pharmaceutical Quality Engineer, you need a solid background in quality assurance, problem-solving, and process improvement, often supported by a degree in engineering, pharmacy, or a related scientific field. Familiarity with regulatory standards (such as GMP, FDA, or ISO 9001), validation software, and quality management systems (QMS) is essential, and certifications like Six Sigma or ASQ CQE can be advantageous. Attention to detail, strong communication, and collaboration skills are crucial for effective cross-functional teamwork and continuous quality improvement. These skills ensure products consistently meet strict regulatory standards for safety and efficacy while supporting efficient and compliant manufacturing operations.

Is pharmaceutical quality engineer a good career?

A pharmaceutical quality engineer plays a key role in ensuring the safety and compliance of pharmaceutical products by developing and maintaining quality systems, conducting audits, and working with regulatory standards. The role typically requires knowledge of Good Manufacturing Practices (GMP), quality management systems, and relevant certifications, offering stable employment with opportunities for advancement in the pharmaceutical industry.

What does a Pharmaceutical Quality Engineer do in the pharmaceutical industry?

A Pharmaceutical Quality Engineer ensures that pharmaceutical products meet quality standards and regulatory requirements by developing, implementing, and monitoring quality systems, conducting audits, and analyzing data. They often work with validation processes, quality control testing, and compliance documentation to maintain product safety and efficacy.

What are the most commonly searched types of Pharmaceutical Quality Engineer jobs in Michigan?

The most popular types of Pharmaceutical Quality Engineer jobs in Michigan are:

What are popular job titles related to Pharmaceutical Quality Engineer jobs in Michigan?

For Pharmaceutical Quality Engineer jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Quality Engineer jobs in Michigan look for?

The top searched job categories for Pharmaceutical Quality Engineer jobs in Michigan are:

Infographic showing various Pharmaceutical Quality Engineer job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 4% Contract, and 2% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $73,248 per year, or $35.2 per hour.

Staff Advanced Quality Engineer

Stryker

Portage, MI • On-site

$89K - $148K/yr

Full-time

Posted 29 days ago


Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

136th of 499 rated machine equipment manufacturers


Job description

Work Flexibility: Hybrid

Staff Advanced Quality Engineer

Portage, MI

Join a team focused on advancing quality throughout the product development lifecycle in a regulated medical device environment. As a Staff Advanced Quality Engineer, you will collaborate with engineering, manufacturing, and project teams to ensure products meet quality, regulatory, and user requirements from concept through commercialization. This role offers the opportunity to provide quality leadership across new product development, design validation, risk management, and product launch activities.

Work Flexibility:
Hybrid: candidates must reside within commuting distance of Portage, MI and be able to work onsite several days per week.

What You Will Do

  • Lead quality engineering activities for new product development programs, ensuring compliance with applicable quality system and regulatory requirements.
  • Guide development teams through design controls, risk management, verification, validation, and product launch processes.
  • Conduct and maintain risk management activities, including risk assessments, risk analyses, and implementation of mitigation strategies throughout product development.
  • Lead human factors engineering activities to support the development of safe, intuitive, and user-focused products.
  • Plan, execute, and approve design validation activities to verify products meet defined user needs and intended use requirements.
  • Support process validation activities and establish quality controls that enable consistent manufacturing performance and long-term product quality.
  • Develop inspection methods and procedures for incoming materials, in-process controls, and finished products to ensure compliance with product specifications.
  • Review technical deliverables, investigate nonconformances and corrective actions, perform root cause analysis, and provide quality representation during cross-functional project reviews.

What You Will Need

Required Qualifications

  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or related engineering discipline.
  • Minimum 4 years of experience in a Quality Engineering or Technical Engineering role within a research and development or manufacturing environment.
  • Experience supporting quality activities within a regulated industry environment.
  • Experience supporting product development, design quality, design controls, or new product introduction activities.

Preferred Qualifications

  • Working knowledge of ISO 13485, ISO14971, Good Manufacturing Practices (GMP), and Good Documentation Practices (GDP).
  • Minimum 3 years of experience as an Advanced Quality Engineer, Design Quality Engineer, or equivalent role.
  • Experience in the medical device, pharmaceutical, biotechnology, or other regulated manufacturing industry.
  • ASQ Certified Quality Engineer (CQE), Certified Reliability Engineer (CRE), Certified Six Sigma Black Belt (CSSBB), GD&T certification, or equivalent professional certification.

$89,300 - $148,800 USD Annual

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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