Supervisor, Quality Control at Stryker

Belfast, Northern Ireland, United Kingdom

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Medical DevicesIndustries

Requirements

Bachelor's Degree in Science, Engineering or related subject
4+ years relevant QA experience in GMP manufacturing environment
Experience managing a team

Responsibilities

Manage team of Quality Inspectors, including leading QA Inspection team through training, development of team members' job roles and responsibilities, and day-to-day management
Provide direction and support to Quality Inspectors
Create a positive team environment with open communication and engaged team members
Communicate and keep team updated on all matters relevant to the business and cell in a timely and appropriate manner
Ensure training happens according to process instructions and occurs in a timely manner
Manage Core Time and Attendance System for Inspection team
Ensure all employees are adequately trained, aware of, and comply with EHS procedures
Ensure employees are aware of and comply with all company policies and procedures
Ensure good housekeeping is maintained in compliance with the 6S Program
Support training programs (GMP/Line Clearance) across the site and develop Inspector Accredited Certification program
Act as local subject expert for review, creation, and training of divisional and corporate procedures
Manage projects focused on quality system improvements, including project planning, personnel recruitment, containment and risk assessment activities, and compilation and communication of project metrics
Develop, manage, and report on Inspection cell KPIs
Continuously improve the performance of the Inspection cells
Own and develop a risk-based approach for inspection plans
Introduce best practices in acceptance and inspection activities (Visual Standards/Measurement techniques/Ops sheets)
Ensure a consistent approach to inspection activities is developed and maintained
Ensure issues and trends identified from Incoming Inspection are addressed with effective root cause corrective actions
Develop, manage, and report on Quality Metrics
Ensure regulatory compliance in area of responsibility to GMP of all medical device regulatory agencies (e.g., FDA, MoH, TUV)
Act as Incoming Inspection point of contact for internal and external audits (e.g., FDA, MoH, TUV)
Ensure compliance to applicable Global Regulations and standards (e.g., ISO, EN, MDR) and Divisional and Corporate procedures

Skills

Key technologies and capabilities for this role

Quality ControlTeam ManagementLeadershipTrainingGMPISOMedical Device RegulationProject ManagementEHS6SInspectionQARisk AssessmentProcess Improvement

Questions & Answers

Common questions about this position

What is the work arrangement for this position?

This is an onsite role at the Belfast site.

What benefits are offered for this role?

The position comes with full Stryker benefits.

What qualifications are required for the Supervisor, Quality Control position?

A Bachelor's Degree in Science, Engineering or related subject and 4+ years of experience are required.

What does the role involve in terms of team management?

The role requires managing a team of Quality Inspectors, providing leadership through training and development, creating a positive team environment with open communication, and handling day-to-day management.

What experience makes a strong candidate for this supervisor role?

Candidates with a Bachelor's Degree in Science or Engineering, 4+ years of experience, and skills in team leadership, regulatory compliance, training, and project management in quality control will stand out.

Stryker

Develops and manufactures medical devices and equipment

About Stryker

Stryker develops and manufactures medical devices and equipment aimed at improving patient care and surgical efficiency. Their products include surgical tools, neurotechnology devices, and orthopedic implants, which are sold directly to hospitals and clinics. Stryker stands out from competitors by focusing on high-quality products and a commitment to advancing healthcare solutions. The company's goal is to enhance the overall healthcare experience for both patients and medical professionals.

Kalamazoo, MichiganHeadquarters

1941Year Founded

$423.3MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Medical & prescription plans

Supplemental health benefits

Flexible Spending accounts

Employee Assistance Program

Short-term & long-term disability

Tuition reimbursement

401(k) plan

Employee Stock Purchase Plan

Risks

Integration challenges from acquisitions may strain Stryker's resources.

Rapid tech advancements risk obsolescence of Stryker's current products.

Regulatory scrutiny on acquisitions could delay Stryker's market entry.

Differentiation

Stryker's acquisitions enhance its minimally invasive surgical solutions portfolio.

Entry into the peripheral vascular segment diversifies Stryker's market presence.

Stryker's focus on AI integration boosts diagnostic accuracy and operational efficiency.

Upsides

Growing demand for minimally invasive solutions aligns with Stryker's strategic acquisitions.

The orthopedic implants market growth benefits Stryker's expanding product line.

Stryker's acquisition of Inari Medical positions it in a high-growth vascular market.

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