Senior Staff Clinical Quality Associate (Onsite)
Stryker
We do not know your resume yet
Upload your resume to unlock your actual match score and identify important JD keywords before applying.
Recruiters may search these ATS Keywords in your resume
Keywords
Job Description
As the Senior Staff Clinical Quality Associate, you will focus on clinical quality, compliance governance, and regulatory readiness across global clinical research activities. You will provide oversight of quality systems, compliance programs, audits, inspections, and clinical processes to ensure clinical services, documentation, and operations align with applicable regulations and quality standards. You will work across functions to identify risks, strengthen controls, and support the continuous improvement of clinical quality programs.
This role provides quality and compliance oversight for clinical research activities, ensuring processes, documentation, systems, and vendor operations remain compliant, inspection-ready, and aligned with global regulatory and quality requirements.
What You Will Do
- Manage clinical quality and compliance programs, establishing milestones, resource plans, and delivery timelines to support on-time execution
- Identify, assess, and communicate compliance risks and control strategies to stakeholders across clinical, quality, and business functions
- Lead internal and external audit and inspection activities, including preparation, execution, follow-up actions, and documentation management
- Participate in regulatory inspections, including inspections of clinical studies conducted by regulatory authorities
- Conduct vendor audits and inspections, maintain audit schedules, and monitor supplier compliance with quality requirements
- Analyze process deviations, determine corrective actions, and update procedures to maintain compliance with applicable regulations and standards
- Develop, maintain, and revise standard operating procedures, work instructions, and quality documentation
- Deliver compliance training, provide guidance on clinical quality requirements, and support continuous improvement initiatives across the clinical organization
What you need
- Bachelor’s degree
- Minimum 7 years of experience in clinical quality, clinical research, quality assurance, compliance, or a related regulated healthcare or life sciences field
- Minimum 5 years of experience supporting quality systems, regulatory compliance programs, audits, or inspections
- Experience supporting clinical studies conducted within a regulated environment
- Experience in medical device, pharmaceutical, biotechnology, or clinical research industries
- Experience participating in regulatory inspections and audit readiness activities
- Experience developing and maintaining standard operating procedures and quality system documentation
- Certified Quality Auditor (CQA), Regulatory Affairs Certification (RAC), or comparable quality or compliance certification
- US5: $115,600 - $192,600 USD Annual
- US30: $143,100 - $238,400 USD Annual
About The Company
Stryker
Stryker is a global leader in medical technologies and, together with our customers, we are driven to make healthcare better. We offer 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. More information is available at stryker.com and careers.stryker.com. Facts: ● 2023 Sales: $20.5 billion ● Industry: Medical Instruments & Supplies ● Employees: 52,000 worldwide ● 40 years of sales growth leading up to 2020 ● 44+ Manufacturing and R&D Locations Worldwide ● $1.4 billion spent on research and development in 2023 ● ~12,900 patents owned globally in 2023 ● Products sold in ~75 countries ● Fortune 500 Company ● 7 consecutive years as one of Fortune's World's Best Workplaces Stryker’s social media community guidelines: https://www.stryker.com/content/m/legal/social-media-community-guidelines/en/index.html Notice Regarding Employee Conduct on Facebook/LinkedIn Meta/LinkedIn does not permit employers to verify or validate “employees” in the (META: “Works at” LinkedIn: “Experience”) section of users’ profiles. Please be aware that the views expressed by individuals on their personal accounts and do not necessarily represent the views of our company. If you encounter any issues with a person claiming to be our employee, we recommend using the “Report Profile” feature. If you’d like to report concerns to our Ethics Hotline, you may do so at: https://app.convercent.com/en-us/LandingPage/b6bb4e84-9fcb-ea11-a974-000d3ab9f296
How to Apply Better for This Job
This section explains the correct next step without forcing sign-in immediately.
Check ATS score before applying
Scan your resume for ATS readability, formatting issues, missing sections, weak keywords, and content gaps.
Customize your resume for this JD
Match your resume with the job description and add sale , audit , stock , compliance , governance , keywords where they fit naturally.
Find similar jobs too
Do not depend on one opening. Use your resume to find similar frontend jobs across relevant job platforms.
Ready with your customized resume?
Once your resume includes the right skills and is ATS-friendly, you can apply directly on the source platform.
Market Insights:Best Software Quality Assurance Engineer Jobs in United States
Find the latest Software Quality Assurance Engineer jobs across top Indian cities. Compare job counts by location and apply where hiring demand is higher.