BD (Becton, Dickinson and Company) Quality Internal Auditor in Murray Hill, New Jersey

The Quality Auditor is responsible for performance of audits in support of the BD Corporate Quality Internal Audit program. In this role, he/she is responsible for carrying out audits under the direction of the Senior Manager and/or Director Corporate Internal Audit. In addition, he/she will work with the sites to ensure submitted objective evidence is compliant with domestic and international regulations, corporate standards, and local procedures. He/she will maintain the audit database to monitor audit program metrics and prepare reports for management.

  • Conduct Corporate Quality Internal Audits to assure compliance with domestic and international medical device standards and regulations, local procedures, and corporate policies/procedures.

  • Follow up with the auditee as required to compile information relating to the audits.

  • Evaluate the adequacy of the provided evidence against the approved Audit Action Plan (AAP). In conjunction with management, develop plans to address inadequate AAP documentation when required

  • Maintain the audit system software database to record the status of all audits and associated actions.

  • Provide periodic reports to management based on the audit statuses and defined metrics.

  • Maintains a high degree of personal professional development through a combination internal and external training and participation in professional associations as appropriate.

  • Bachelor’s degree in Engineering, Chemistry, Biology, or other related discipline

  • A minimum of 3+ years work experience in the Quality organization of a Medical Device and/or Pharmaceutical company

  • A minimum of 2+ years experience in with auditing compliance with domestic and international regulations for medical devices or pharmaceuticals.

  • Knowledge and experience in CAPA; Root Cause Investigation; Validation (Process, Test Method, Software, and Design); Environmental Monitoring; Sterilization (EtO, Irradiation)

  • Knowledge and ability to apply international regulations and standards of FDA QSR, ISO 13485, EU MDR, and ISO 14971 standards

  • Excellent verbal and written communication skills

  • Demonstrated ability to effectively collaborate and partner with all levels of management while maintaining an appropriate assertive style is critical.

  • Strong analytical skills

  • Effective project management and organizational skills are essential.

  • One of the below certifications or equivalent:

  • Certified Quality Auditor/ISO Lead Auditor Certified

  • Certified Quality Engineer

  • Certified Quality Manager

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ID: 2018-11799

Career Level: experienced

Division Name: BDI Corporate

Relocation Available?: No

External Company Name: C.R. Bard, Inc.

External Company URL: www.crbard.com

Street: 730 Central Ave

C. R. Bard, Inc. (NYSE: BCR) is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 13,000 people around the world. Founded in 1907, we pioneered many devices that are now the cornerstones of modern healthcare.

We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Bard is a M/F, Disabled and Vet EEO/AA Employer.

Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world.