Mid Level Senior Quality Manager Jobs
Mid level senior quality manager jobs go to professionals ready to own quality programs end to end, lead cross-functional audits, and guide junior team members without close oversight. Openings run across Biotechnology & Pharmaceuticals, Technology & Software, and Manufacturing, with 20% remote or hybrid availability and employers like CooperSurgical, Boston Scientific, and Katalyst Healthcares & Life Sciences hiring at this level now.
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Showing 5 of 121+ Mid Level Senior Quality Manager jobs
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.The Senior Quality Management System Specialist will help design, maintain, and continuously improve a quality management system that supports regulatory approval and business growth across global markets. You’ll collaborate across functions to ensure quality processes are not only compliant, but practical, efficient, and future‑ready. Activities include Quality System documentation, Internal Quality Agreements, Supplier Quality Agreements, and general QMS activities related to Mergers and Acquisitions. This role is Hybrid in Portage, Michigan.
What You Will Do
- Support and maintain a compliant Quality Management System aligned with global medical device regulations to enable product certification and regulatory clearances.
- Develop and update quality system processes, procedures, and documentation to reflect business needs and regulatory expectations.
- Assess and quantify quality system requirements to optimize structure, integration, and scalability.
- Identify and implement continuous improvement opportunities that increase efficiency and effectiveness of quality processes.
- Support management review, quality planning forums, and related governance activities with data-driven inputs.
- Partner with stakeholders to ensure quality processes reflect actual operational activities, including support for new product development.
- Prepare for and support internal, external, and third‑party quality system audits, including responses and follow‑up actions.
- Contribute to quality system training content and delivery to ensure effective adoption across the organization.
What You Will Need
- Bachelor’s degree in science, engineering, business, or a related discipline.
- 3+ years of experience working in a regulated industry environment.
Preferred
- Knowledge of U.S. and international medical device regulatory requirements.
- Experience supporting quality systems such as audits, management review, quality planning, and corrective action processes.
- Experience supporting regulated information systems or quality systems change control.
- Exposure to good manufacturing and distribution practices within a quality environment.
United States of America Pay Ranges:
- USN: $72,500 - $120,900 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.The Senior Quality Management System Specialist will help design, maintain, and continuously improve a quality management system that supports regulatory approval and business growth across global markets. You’ll collaborate across functions to ensure quality processes are not only compliant, but practical, efficient, and future‑ready. Activities include Quality System documentation, Internal Quality Agreements, Supplier Quality Agreements, and general QMS activities related to Mergers and Acquisitions. This role is Hybrid in Portage, Michigan.
What You Will Do
- Support and maintain a compliant Quality Management System aligned with global medical device regulations to enable product certification and regulatory clearances.
- Develop and update quality system processes, procedures, and documentation to reflect business needs and regulatory expectations.
- Assess and quantify quality system requirements to optimize structure, integration, and scalability.
- Identify and implement continuous improvement opportunities that increase efficiency and effectiveness of quality processes.
- Support management review, quality planning forums, and related governance activities with data-driven inputs.
- Partner with stakeholders to ensure quality processes reflect actual operational activities, including support for new product development.
- Prepare for and support internal, external, and third‑party quality system audits, including responses and follow‑up actions.
- Contribute to quality system training content and delivery to ensure effective adoption across the organization.
What You Will Need
- Bachelor’s degree in science, engineering, business, or a related discipline.
- 3+ years of experience working in a regulated industry environment.
Preferred
- Knowledge of U.S. and international medical device regulatory requirements.
- Experience supporting quality systems such as audits, management review, quality planning, and corrective action processes.
- Experience supporting regulated information systems or quality systems change control.
- Exposure to good manufacturing and distribution practices within a quality environment.
United States of America Pay Ranges:
- USN: $72,500 - $120,900 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
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Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals18
- Technology & Software16
- Manufacturing15
- Medical Devices12
- Electronics & Hardware12
Mid Level Senior Quality Manager Jobs: Frequently Asked Questions
How do I get a mid level senior quality manager job?
Position your existing experience around ownership and outcomes: highlight audits you led independently, corrective action plans you designed, or quality systems you improved with measurable results. Tailor your resume to show you can manage quality programs with limited oversight, not just execute tasks assigned to you. Certifications like CQE or ASQ credentials strengthen your candidacy alongside demonstrated project leadership.
Which companies hire mid level senior quality managers?
Companies hiring mid level senior quality managers right now include CooperSurgical, Boston Scientific, and Katalyst Healthcares & Life Sciences, based on current listings on Migrate Mate as of September 2026. Hiring at this level covers manufacturers, medical device firms, and consumer goods companies that need quality professionals who can run programs independently rather than supporting them.
Are there remote mid level senior quality manager jobs?
Yes, though on-site roles still dominate in highly regulated industries. About 20% of mid level senior quality manager openings are remote or hybrid as of September 2026, concentrated in roles focused on quality systems, documentation, and supplier management rather than floor-level inspection or hands-on manufacturing oversight.
How do I move up to a mid level senior quality manager role?
Growth into mid level comes from building a record of independent project ownership, not just task completion. Seek out chances to lead an internal audit, own a corrective action process, or drive a quality improvement initiative from diagnosis to close. Pair that hands-on scope with a recognized quality certification, and demonstrate that your decisions reduce risk rather than escalate it.
Which industries hire the most mid level senior quality managers?
Mid Level senior quality manager roles concentrate in Biotechnology & Pharmaceuticals, Technology & Software, and Manufacturing, based on current listings on Migrate Mate as of September 2026. Those sectors share strict regulatory requirements, supplier complexity, or product safety standards that create sustained demand for quality professionals who can manage programs with real autonomy.