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Remote Pharmaceutical Quality Engineer Jobs in Michigan

Remote Duration: 4-6 weeks Commitment: 20+ hours/week Role Responsibilities * Evaluate AI-generated ... Provide expert feedback on quality standards and logistics coordination. * Leverage real-world ...

(Remote) Senior Software Engineer

Wyoming, MI · Remote

$111K - $146K/yr

... quality, and mentoring within a fast-paced healthcare technology environment. The role leads ... This remote role welcomes candidates anywhere in the US. Salary: 110K - 135K What your impact will ...

... remote teams * Strong communication skills Bonus Points * Experience with C# programming and JAVA ... where quality is taken seriously; working with dedicated and very smart developers; if you like ...

(Remote) Senior Software Engineer

Wyoming, MI · Remote

$111K - $146K/yr

... quality, and mentoring within a fast-paced healthcare technology environment. The role leads ... This remote role welcomes candidates anywhere in the US. Salary: 110K - 135K What your impact will ...

Quality Assurance Analyst

Wyoming, MI · On-site +1

$55K - $65K/yr

Ability to work effectively with developers, support staff, product stakeholders, and other cross ... Ability to manage priorities, meet deadlines, and work independently in a remote team environment.

$55K - $65K/yr

Ability to work effectively with developers, support staff, product stakeholders, and other cross ... Ability to manage priorities, meet deadlines, and work independently in a remote team environment.

Quality Assurance Analyst

Three Rivers, MI · On-site +1

$55K - $65K/yr

Ability to work effectively with developers, support staff, product stakeholders, and other cross ... Ability to manage priorities, meet deadlines, and work independently in a remote team environment.

The Product Engineering area is responsible for designing, writing, testing and deploying the code ... Design, build, and refine AI use cases including guardrails, evaluation frameworks, and quality ...

Remote As a Salesforce Software Engineer, you will play a key role in shaping how our U.S ... Coordinate QA and UAT testing activities to verify and validate new functionality before release.

Remote As a Salesforce Software Engineer, you will play a key role in shaping how our U.S ... Coordinate QA and UAT testing activities to verify and validate new functionality before release.

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Remote Pharmaceutical Quality Engineer information

What is a remote pharmaceutical quality engineer?

A Remote Pharmaceutical Quality Engineer is a professional responsible for ensuring the quality and compliance of pharmaceutical products and manufacturing processes, while working from a remote location. They review documentation, monitor processes, conduct virtual audits, and collaborate with on-site teams to ensure products meet regulatory standards such as FDA or EMA requirements. Their work helps maintain the safety, efficacy, and quality of pharmaceutical drugs and devices throughout development and production. Remote Quality Engineers use digital tools and systems to manage quality processes and communicate effectively with stakeholders.

What are the key skills and qualifications needed to thrive as a remote pharmaceutical quality engineer?

To thrive as a Remote Pharmaceutical Quality Engineer, you need a solid background in pharmaceutical sciences, quality assurance, and regulatory compliance, typically supported by a degree in engineering, pharmacy, or a related field. Familiarity with industry standards such as GMP, FDA regulations, and proficiency with quality management systems (QMS) and digital auditing tools are essential. Strong attention to detail, problem-solving abilities, and effective communication are vital soft skills for collaborating remotely and ensuring product quality. These skills ensure regulatory compliance, product safety, and efficient remote teamwork in a highly regulated industry.

What are the typical challenges faced by a remote pharmaceutical quality engineer, and how can they be addressed?

Remote Pharmaceutical Quality Engineers often navigate challenges such as maintaining effective communication with on-site teams, ensuring compliance with strict regulatory standards, and managing documentation digitally. To address these, it's important to establish clear communication channels, participate in regular virtual meetings, and use secure document management systems. Building strong relationships with cross-functional teams and staying up to date with the latest regulatory changes also help in ensuring quality and compliance from a remote setting.

What is the difference between Remote Pharmaceutical Quality Engineer vs Remote Quality Assurance Specialist?

AspectRemote Pharmaceutical Quality EngineerRemote Quality Assurance Specialist
CredentialsDegree in Pharmacy, Chemistry, or related field; certifications like CQE or ASQDegree in Quality Management, Life Sciences, or related; similar certifications
Work EnvironmentPharmaceutical manufacturing, R&D labs, compliance departmentsQuality audits, document review, process validation in various industries
Employer & IndustryPharmaceutical companies, biotech firms, contract manufacturersPharmaceutical, biotech, medical device, and manufacturing sectors

The Remote Pharmaceutical Quality Engineer focuses on ensuring product quality through design, validation, and compliance in pharmaceutical manufacturing. In contrast, the Remote Quality Assurance Specialist emphasizes maintaining quality standards via audits, documentation, and process reviews across industries. Both roles require similar credentials and often work within the same industry, but their core responsibilities differ slightly.

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

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

What cities in Michigan are hiring for Remote Pharmaceutical Quality Engineer jobs?

Cities in Michigan with the most Remote Pharmaceutical Quality Engineer job openings:

Senior Staff Software Advance Quality Engineer

Detroit, MI • On-site, Remote


Stryker
Medical Equipment and Supplies Manufacturing • 10K+ employees

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

131st of 495 rated machine equipment manufacturers

Great coworkers

People enjoy working here

Good employer


Full-time

Re-posted 3 days ago


Job description

Work Flexibility: Remote or Hybrid or OnsiteIt's Time to Join Stryker!Why Join Us

In this role, you will help shape software quality practices across a growing portfolio of digital and connected solutions. You will influence how software teams incorporate quality, compliance, security, and risk management into development while establishing scalable processes that support innovation and efficient delivery.

Stryker is seeking a Senior Staff Software Quality Assurance Engineer to support our Digital Platform Hub. In this role, you will partner with software R&D teams to establish, implement, and improve quality processes across digital, connected, SaaS, and cloud-based products.

You will provide quality-system guidance throughout the software development lifecycle, support audit and compliance readiness, and translate regulatory and industry requirements into practical, scalable processes. You will collaborate with R&D, Product Security, Privacy, Regulatory Affairs, IT, Operations, and Quality to enable efficient and compliant software delivery.

This is not a software testing or test-execution role. This position focuses on software quality systems, SDLC governance, risk management, audit readiness, and process improvement.

What You Will DoSoftware Quality Systems and Process Leadership
  • Serve as a software quality and compliance subject matter expert for software, SaaS, cloud-hosted, and connected products.
  • Guide software R&D teams through applicable Quality Management System processes, procedures, and documentation requirements.
  • Develop, maintain, and improve software quality procedures, work instructions, templates, and guidance documents.
  • Identify process gaps and lead continuous-improvement initiatives across the software development lifecycle.
  • Translate regulatory, quality, security, and compliance requirements into practical development processes.
  • Establish scalable quality practices that support compliant and efficient software delivery.
  • Assess emerging regulations and standards and determine their impact on software-development processes.
Software Lifecycle and Risk Management
  • Provide quality guidance throughout requirements, design, development, change control, release, maintenance, and retirement activities.
  • Participate in design reviews, risk assessments, change assessments, and release-readiness reviews.
  • Ensure software quality and compliance risks are identified, evaluated, documented, and appropriately addressed.
  • Integrate quality and risk-management practices into Agile, DevOps, and CI/CD environments.
  • Review software quality deliverables and provide clear, risk-based guidance to project teams.
Audit and Compliance Readiness
  • Support readiness activities for SOC 2, ISO 27001, HIPAA, FDA, and other applicable frameworks.
  • Partner with control owners to ensure controls are implemented, maintained, and supported by objective evidence.
  • Support internal and external audits through gap assessments, evidence collection, auditor interaction, and remediation.
  • Lead or support investigations, root-cause analysis, corrective actions, and effectiveness monitoring related to software quality issues.
Cross-Functional Leadership
  • Partner with Software Engineering, Product Security, Privacy, Regulatory Affairs, IT, Operations, and Quality teams.
  • Mentor and coach teams on quality-system requirements, software risk management, and compliant development practices.
  • Influence technical and business stakeholders without direct authority.
  • Resolve conflicts between development priorities, delivery timelines, and quality or compliance requirements.
  • Promote the integration of quality, security, compliance, and risk management into software-development decisions.
What You Need
  • Bachelor's degree in Software Engineering, Computer Science, Engineering, Quality, or a related technical discipline is required.
  • Six or more years of professional experience in software quality, quality systems, software compliance, audit, or a related field supporting software, SaaS, cloud-based, or connected products is required.
  • Experience developing, implementing, maintaining, or improving software quality processes or procedures is required.
Preferred Qualifications (You Do Not Need to Have All of These)
  • Master's degree or another advanced technical degree.
  • Professional experience in software engineering or development before transitioning into software quality, compliance, or quality systems.
  • Strong understanding of the software development lifecycle, including change control, risk management, audit readiness, and Quality Management System processes.
  • Experience partnering with software development or R&D teams to implement or improve software quality processes.
  • Experience supporting regulated software products, preferably within medical devices, digital health, healthcare technology, or another compliance-driven industry.
  • Experience with SOC 2, ISO 27001, HIPAA, FDA software expectations, 21 CFR Part 11, IEC 62304, ISO 14971, ISO 13485, or comparable frameworks.
  • Working knowledge of cloud platforms, DevOps, CI/CD, and software security controls.
  • Experience leading audits, gap assessments, remediation activities, quality investigations, or corrective and preventive actions.
  • Demonstrated ability to influence cross-functional teams, communicate complex requirements, and lead process improvements without direct authority.
  • Professional certification such as CSQE, CQE, CQA, or an equivalent quality or compliance credential.

United States of America Pay Ranges:

  • Puerto Rico: $102,600 - $171,000 USD Annual
  • USN: $118,000 - $196,700 USD Annual
  • US5: $123,900 - $206,500 USD Annual
  • US10: $129,800 - $216,400 USD Annual
  • US15: $135,700 - $226,200 USD Annual
  • US20: $141,600 - $236,000 USD Annual
  • US30: $153,400 - $255,700 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

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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