Supervisor, Quality Control

Stryker Group; Belfast; On-site; GBP 45,000 - 65,000; Full time

Job summary

A leading medical device company in Belfast is looking for a Quality Inspection Manager. The role entails managing a team of Quality Inspectors, ensuring compliance with global regulations and standards, and supporting training programs. The ideal candidate will have at least 4 years of QA experience in a GMP environment and a relevant Bachelor's Degree. Competitive benefits are offered in this permanent position.

Benefits

Full company benefits

Qualifications

• 4+ years of relevant QA experience in GMP manufacturing environment.
• Experience managing a team.

Responsibilities

• Manage a team of Quality Inspectors.
• Lead QA Inspection team through training and development.
• Ensure compliance to applicable Global Regulations.
• Develop and report on Inspection cell KPIs.
• Act as point of contact for internal and external audits.

Skills

Team management

Project management

Quality Assurance

Communication

Education

Bachelor's Degree in Science, Engineering or related subject

Job description

This is a permanent role in our Belfast site with full Stryker benefits.

This position is responsible for the development, management and leadership of the Inspection team.

This will be the key point of contact for all quality functions and business areas that interact with the Inspection teams.

They will ensure compliance to applicable Global Regulations and standards (e.g. ISO, EN, and Medical Device Regulation (MDR) requirements).

Inspection Team

• Manage team of Quality Inspectors
• Lead QA Inspection team through training, development of team members job roles and responsibilities, and day to day management of the team
• Provide direction and support to Quality Inspectors
• Create a positive team environment with open communication and engaged team members
• Communicate & keep team updated on all matters relevant to the business and cell in a timely and appropriate manner
• Ensure that training happens according to the process instructions and occurs in a timely manner
• Manage Core Time and Attendance System for Inspection team
• Ensure that all employees are adequately trained, are aware of, and comply with EHS procedures
• Ensure that employees are aware of and comply with all company policies and procedures
• Ensure that good housekeeping is maintained in compliance with the 6S Program

Training

• Support training programs (GMP/Line Clearance) across the site. Development of Inspector Accredited Certification program.
• Support/ act as local subject expert for review, creation and training of divisional and corporate procedures.

Project Management

• Project management in areas that focus on quality system improvements that systemically improve the level of quality and compliance within the Inspection department
• Project management activities include: Project planning, personnel recruitment, containment and risk assessment activities and the compilation and communication of project metrics.

Productivity and Process Improvements

• Develop, Manage and report on Inspection cell KPI’s
• Continuously improve the performance of the Inspection cells.
• Ownership and development of a risk-based approach for the inspection plans
• Introduction of best practices in acceptance and inspection activities (Visual Standards/Measurement techniques Ops sheets).
• Ensure that a consistent approach to inspection activities is developed and maintained.

Trending

• Ensure issues & trends identified from Incoming Inspection are addressed, and effective root cause corrective actions put in place.
• Develop, Manage and report on Quality Metrics.
• Regulatory Compliance:
• Ensure Regulatory compliance in area of responsibility to GMP of all medical device regulatory agencies (i.e. FDA, MoH, TUV, etc.).
• Act as Incoming Inspection point of contact for internal and external audits (i.e. FDA, MoH, TUV, etc.). Ensure compliance to Divisional and Corporate procedures.

Qualifications

• Bachelor's Degree in Science, Engineering or related subject.
• 4+ year’s relevant QA experience in GMP manufacturing environment and experience managing a team