About Company
Johnson & Johnson is a global leader in healthcare, dedicated to addressing some of the world’s most pressing health challenges. With a rich history spanning over 130 years, our unwavering commitment to innovation and patient well-being has driven us to create life-changing products and solutions across Consumer Health, Pharmaceuticals, and Medical Devices. We proudly touch the lives of billions worldwide. Our Ethicon facility in Livingston, Scotland, plays a crucial role in delivering cutting-edge medical devices that improve surgical outcomes and patient recovery. At Johnson & Johnson, we believe in the power of diversity, inclusion, and a collaborative spirit to drive progress and foster a culture where every employee can thrive and make a meaningful impact. Join our team and be part of a legacy of care and innovation that shapes the future of health.
Job Description
Are you a meticulous and dedicated professional with a keen eye for detail? Johnson & Johnson, a world-renowned leader in healthcare, is immediately hiring a Quality Inspector to join our dynamic team in Livingston, Scotland. This is an exceptional opportunity to contribute directly to the safety and efficacy of life-saving medical devices. As a Quality Inspector, you will be an integral part of our manufacturing process, ensuring that every product meets our rigorous quality standards and complies with global regulatory requirements. You will perform critical inspections at various stages, identify potential defects, and collaborate with cross-functional teams to uphold the highest levels of product integrity. We are looking for an individual who is passionate about quality, thrives in a fast-paced environment, and is committed to making a tangible difference in patient care. Your work will directly impact millions of lives, ensuring that our products are not only effective but also impeccably safe and reliable for healthcare professionals and patients alike. If you possess a strong understanding of quality control principles and are ready to embark on a rewarding career with a company that values innovation, integrity, and a healthy work-life balance, we encourage you to apply. This role offers continuous learning and development opportunities within a supportive and forward-thinking team that prioritizes excellence.
Key Responsibilities
- Conduct thorough inspections of raw materials, in-process components, and finished medical devices according to established specifications, drawings, and quality standards.
- Utilize precision measurement tools and techniques (e.g., calipers, micrometers, gauges, optical comparators) to verify product dimensions and characteristics.
- Document inspection results accurately and comprehensively, including identifying and reporting non-conformances and potential deviations.
- Initiate and participate in root cause analysis for identified defects and support the implementation of corrective and preventive actions (CAPA).
- Collaborate closely with production, engineering, and quality assurance teams to resolve quality issues and implement continuous improvements.
- Ensure strict compliance with Good Manufacturing Practices (GMP), ISO 13485 standards, FDA regulations, and other relevant quality system requirements.
- Maintain, verify, and calibrate inspection equipment as per established procedures and schedules.
- Participate in continuous improvement initiatives focused on enhancing quality processes, efficiency, and overall product reliability.
- Provide training and guidance to production staff on quality procedures, standards, and best practices.
- Perform final release inspections for products destined for shipment to ensure compliance with all release criteria.
Required Skills
- Proven experience (minimum 2 years) as a Quality Inspector or similar role in a manufacturing environment, preferably within medical devices, pharmaceuticals, or a similarly regulated industry.
- Strong understanding of quality control principles and methodologies.
- Proficiency in using various inspection tools (e.g., calipers, micrometers, height gauges, optical comparators).
- Ability to accurately read and interpret technical drawings, blueprints, and engineering specifications.
- Excellent attention to detail and a methodical, analytical approach to problem-solving.
- Strong written and verbal communication skills for effective collaboration and documentation.
- Basic computer proficiency, including experience with Microsoft Office Suite (Word, Excel).
- Demonstrated ability to work independently while also being an effective team player.
Preferred Qualifications
- Certification in Quality Inspection (e.g., ASQ Certified Quality Inspector).
- Experience with ISO 13485 and FDA regulations governing medical device manufacturing.
- Familiarity with statistical process control (SPC) techniques.
- Knowledge of lean manufacturing or Six Sigma principles.
- Vocational training or a technical qualification in a relevant engineering or manufacturing field.
Perks & Benefits
- Competitive salary and comprehensive benefits package.
- Generous paid time off and holidays.
- Robust pension scheme with significant company contributions.
- Medical, dental, and vision insurance coverage.
- Extensive opportunities for professional development and career advancement within a global organization.
- Employee assistance program for personal and professional support.
- On-site amenities (e.g., cafeteria, wellness programs, gym access – may vary by specific location).
- Employee discount programs on a range of products and services.
- A vibrant culture of innovation, collaboration, and ethical conduct committed to making a difference in global health.
How to Apply
To apply for this exciting opportunity and become a part of the Johnson & Johnson team, please click on the application link below. We encourage all qualified candidates to submit their application promptly to be considered.