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Staff CAPA Specialist

Stryker

Arlington, TNJob$83–139K/yrTracked 1mo agoSeen in employer's feed 3 days ago

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At a glance

Compensation
$83–139K/yr
Location
Arlington, TN
Work Authorization
Not specified

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Stryker is hiring a Staff CAPA Specialist. The Staff CAPA Specialist will leverage strong CAPA and quality systems expertise within a regulated environment. This role involves collaborating with stakeholders, navigating complex quality challenges, and driving continuous improvement initiatives. The ideal candidate will demonstrate exceptional attention to detail and effectively balance compliance requirements with business needs in a matrixed organization.

Key focus areas include Review and approve NC and CAPA records for completeness, effectiveness, accuracy, timeliness, and compliance., Approve documentation changes, extensions, and corrective action plans., and Serve as local SME and process owner for NC/CAPA processes and procedures..

Successful candidates bring Bachelor's Degree In Engineering, Bachelor's Degree In Science, and Bachelor's Degree In Related Technical Discipline. Important skills include CAPA, Quality Systems Expertise, Problem Solving, Influence Stakeholders, Navigate Complex Quality Challenges, and Drive Continuous Improvement Initiatives. Preferred (not required): FDA Quality System Regulations (21 CFR Part 820), ISO 13485, MDSAP, and Global Regulatory Requirements.

Skills & qualifications

RequiredNice to have

Skills

CAPAQuality Systems ExpertiseProblem SolvingInfluence StakeholdersNavigate Complex Quality ChallengesDrive Continuous Improvement InitiativesAttention to DetailBalance Compliance Requirements With Business NeedsApprove Documentation ChangesApprove ExtensionsApprove Corrective Action PlansEnsure Compliance With Corporate and Local Quality RequirementsCoach and Train Teams on Global eCAPA SystemPromote Effective Root Cause AnalysisPromote Human Error Reduction MethodsImprove Quality SystemsImprove ReportingImprove Operational EffectivenessIdentify Process Improvements Aligned With Corporate Quality StrategyLead and Support Cross-Site Quality ProjectsSupport Development of Global Quality Procedures and StandardsMonitor Quality MetricsReport Updates to Quality LeadershipLead Quality Governance ActivitiesEnsure Compliance With Global Quality Metrics and Reporting ExpectationsLead Audit PreparationLead Audit ParticipationLead Audit Follow-Up for Internal AuditsSupport Regulatory Agency and Auditor InteractionsMaintain Readiness and Compliance With Applicable Regulatory StandardsQuality Management SystemsProject ManagementCommunicationStakeholder ManagementWork IndependentlyManage Multiple PrioritiesMicrosoft WordExcelPowerPointLearn and Effectively Utilize New Software SystemsFDA Quality System Regulations (21 CFR Part 820)ISO 13485MDSAPGlobal Regulatory RequirementsInteracting With Regulatory AgenciesInteracting With Notified BodiesKnowledge of Supporting Quality ProcessesManagement ReviewQuality PlanningLeading Projects Within a Global Matrix Organization

Qualifications

Bachelor's Degree in EngineeringBachelor's Degree in ScienceBachelor's Degree in Related Technical Discipline4+ Years Experience in CAPA4+ Years Experience in Quality Systems4+ Years Experience in Engineering4+ Years Experience in Related Function Within a Regulated IndustryMaster's DegreeExperience Within the Medical Device IndustryExperience Within the Pharmaceutical IndustryExperience Within Other Highly Regulated Industries

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

We are seeking a Staff CAPA Specialist with strong CAPA and quality systems expertise who excels in a regulated environment. The ideal candidate is a collaborative problem solver who can influence stakeholders across functions, navigate complex quality challenges, and drive continuous improvement initiatives. This individual thrives in a matrixed organization, demonstrates exceptional attention to detail, and effectively balances compliance requirements with business needs.

What You Will Do

  • Review and approve NC and CAPA records for completeness, effectiveness, accuracy, timeliness, and compliance.

  • Approve documentation changes, extensions, and corrective action plans.

  • Serve as local SME and process owner for NC/CAPA processes and procedures.

  • Ensure compliance with corporate and local quality requirements.

  • Partner with teams to guide investigations and CAPA activities through all process stages.

  • Coach and train teams on CAPA principles, problem solving, and the global eCAPA system.

  • Mentor users and quality professionals on CAPA best practices.

  • Promote effective root cause analysis, problem solving, and human error reduction methods.

  • Improve CAPA processes, quality systems, reporting, and operational effectiveness.

  • Identify process improvements aligned with corporate quality strategy.

  • Lead and support cross-site, multi-site, and global quality projects.

  • Support development of global quality procedures and standards.

  • Monitor site CAPA performance and quality metrics.

  • Report updates to quality leadership and business review forums.

  • Lead CAPA review board meetings and quality governance activities.

  • Ensure compliance with global quality metrics and reporting expectations.

  • Lead audit preparation, participation, and follow-up for internal, corporate, customer, and third-party audits.

  • Represent local CAPA processes during inspections and audits.

  • Support regulatory agency and auditor interactions as a quality systems expert.

  • Maintain readiness and compliance with applicable regulatory standards.

What You Need

  • Bachelor's degree in Engineering, Science, or a related technical discipline.

  • Minimum 4 years of experience in CAPA, Quality Systems, Engineering, or a related function within a regulated industry.

  • Strong knowledge of Quality Management Systems (QMS) and CAPA processes.

  • Experience leading investigations, corrective actions, and continuous improvement initiatives.

  • Strong project management, communication, and stakeholder management skills.

  • Ability to work independently with minimal supervision while managing multiple priorities.

  • Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint.

  • Ability to learn and effectively utilize new software systems.

  • Fluent English communication skills (written and verbal).

Preferred

  • Master's degree preferred.

  • Experience within the medical device, pharmaceutical, or other highly regulated industries.

  • Strong knowledge of FDA Quality System Regulations (21 CFR Part 820), ISO 13485, MDSAP, and other applicable global regulatory requirements.

  • Experience interacting with regulatory agencies and notified bodies such as FDA, BSI, TÜV, or Ministry of Health representatives.

  • Knowledge of supporting quality processes including audits, management review, and quality planning.

  • Demonstrated success leading projects within a global matrix organization.

  • Advanced analytical, critical thinking, and problem-solving capabilities.

  • Experience serving as a CAPA Process Owner, Quality Systems Specialist, or eCAPA Super User.

  • Previous experience leading cross-functional and global quality initiatives.

United States of America Pay Ranges:

  • USN : $83,300 - $138,800 USD Annual

View the U.S. work location and transparency guide (https://view.stryker.com/viewer/fcd609f31e39eac44598615224ec7216?iid=69deda99678eb495e0710914#1) 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.

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.

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