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Quality Compliance Leader

Job LocationPlymouth
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

Job DescriptionBe part of something bigger!BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country aroundthe world to address some of the most challenging global health issues.About the roleResponsible for the management and maintenance of the CAPA, Management Review, Supplier Management, Supplier Quality Assurance and Internal Audit functions, also responsible for ensuring that BD Plymouth are compliant with relevant regulations and BD / IDS/ SM procedures. This position reports to the Associate Director Quality Management.YOUR KEY RESPONSIBILITIESManagement of plant CAPA program as Site CAPA Leader. Reporting of trends at Plant CAPA Board and Management review meetings. Support for CAPA Owners and Approvers through training and mentoring.Management, implementation, and continual improvement of the site internal audit programme as Audit Program Manager. Reporting on trends/ developments for SLT and Management Review meetings.Coordination of external audits conducted by Governmental agencies, Notified Bodies, customers and other parties ensuring successful execution.Leading Supplier Management at BD Plymouth:

  • Manage Supplier Management Program (assessments, audits, surveys) in accordance with the relevant national standards, international standards and Becton Dickinson policies and procedures.
  • Manage Supplier Quality Engineer to identify, analyse and improve supplier performance in line with BD Plymouth Goals and Objectives.
  • Manage Supplier Quality Department to ensure all incoming testing is conducted in accordance with the relevant national standards, international standards and Becton Dickinson policies and procedures. In case of noncompliance work with BD production andsupply chain, follow-up with suppliers.
About You
  • Our ideal candidate will be experienced in the Quality/Regulatory arena at supervisory level and Lead Auditor Qualified to ISO13485 (Medical Devices).
  • Exposure to the requirements of ISO 13485 and FDA 21 CFR 820
  • B.Sc. (Hons) degree, preferably in Science, Quality Assurance or Business Management. If not in QA, then some form of Quality Management qualification is required.
Click on apply if this sounds like you!Why join usA career at BD means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their lifes purpose through the work that they do every day.You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards programwhich includes competitive pay, benefits, continuouslearning, recognition, career growth, and life balance componentsis designed to support the varying needs of our diverse and global associates.Becton, Dickinson and Company is an Equal Opportunity Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status,affectional or sexual orientation, gender identity or expression, genetics, disability, or any other protected status.Primary Work LocationGBR Plymouth - Belliver Industrial EstateWork ShiftGB-PLY Office Staff 0830-1630 (United Kingdom)

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