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Job Function: Supply Chain Engineering
Job Sub Function: Quality Engineering
Job Category: People Leader
All Job Posting Locations: Leeds, West Yorkshire, United Kingdom
Job Description:
J&J MedTech is recruiting for a Quality Operations Team Lead reporting to the Site Quality Leader within the Quality department and to be based in Leeds (UK).
JOB SUMMARY
Part of the Quality team reporting into the Site Quality Lead. Quality Operations Team Leader is accountable for the day to day Quality Engineering effort for all manufacturing processes. This will include managing projects designed to identify and implement process improvements within the area, validation and receiving inspection area.
The Quality Operations Team Leader will utilize Quality Engineering tools and practices for the effective and efficient development, transfer and maintenance of products/processes throughout the product lifecycle. The incumbent will also utilize Quality Engineering principles and problem-solving skills to improve and maintain products/processes that are aligned with the overall Quality and Business vision. This person will support processes in base business and supervise or lead Engineers & Technicians.
This position requires an in-depth knowledge of both Quality, Compliance and Validation, in alignment with ISO13485, FDA QSRs and the Medical Devices Directive.
DUTIES & RESPONSIBILITIES
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
1. Lead Quality Engineering effort for all manufacturing processes. This will include managing projects designed to identify and implement process improvements within the area.
2. Lead Receiving Inspection function, ensuring efficient and compliant processes are deployed.
3. Lead the quality activities for all product and process validation activities for J&J MedTech, Leeds. Develop and maintain state of the art protocols and procedures and ensure correct implementation across site. Provide technical expertise for all areas on relevant IQ/OQ/PQ protocol issues.
4. Lead site wide activities aimed at maintaining Part 11 Compliance.
5. Assess the need for risk mitigation techniques based on product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc. Determine effectiveness of these techniques on previously implemented improvements.
6. Support the quality effort for all New Product Introduction activities to ensure that all quality aspects of process design are addressed. Document and maintain in good order all relevant sections of Device Design History File and DMR as directed.
7. Develop and utilise DFMEA/PFMEA and other QA risk analysis techniques in order to minimise potential risk during development/implementation activity. Work with Production and Technical Support to develop and implement appropriate process control plans.
8. Partner with Supplier Quality, Technical Support, Design QE and Purchasing to ensure that all Supplier generated products and components are compliant.
9. Partner with Supplier Quality, Technical Support, Design QE and Purchasing to ensure that all Supplier generated design changes are managed and documented in a compliant manner.
10. Ensure compliance with all Documented Quality system, FDA QSR’s and ISO 13485 requirements during day to day and assigned audit/CAPA activities.
11. Maintain a good level of housekeeping in designated areas, and observe all Health and Safety at work requirements. Operate within the company’s standard procedures where applicable, and review, maintain and create appropriate procedures for sphere of activity.
12. Responsible for communicating business related issues or opportunities to next management level.
13. For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
14. Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
15. Performs other duties assigned as needed.
EXPERIENCE AND EDUCATION
• A minimum of a Bachelor’s Degree, preferably in Engineering or related technical field. Generally, requires 5-8 years related experience.
• Experience working in both an FDA and European regulatory environment is preferred.
• Relevant experience working in a manufacturing/operations environment.
REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS
• Good technical understanding of manufacturing equipment and processes is required.
• In-depth knowledge and experience of product/process Risk Management (FDA and ISO standards).
• Technical training and experience using Statistics, Lean and Six Sigma Methodologies is required including Measurement System Analysis, SPC, DOEs, Reliability, etc.
• Strong knowledge of statistical software packages is preferred with the ability to review, analyze and present data that drives decision making.
• The ability to perform "hands on" troubleshooting and problem solving is required. The ability to think on the feet and provide sound judgment is highly desired.
• Understanding of the NPI (New Product Introduction) process and Process Validation is preferred.
• A thorough understanding of GMP/ISO regulations and validation regulations is preferred.
• Strong mentoring, coaching and leadership skills are required.
• Demonstrated project management and project leadership abilities.
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