Valeant Pharmaceuticals Sr. Supplier Quality Auditor in Bridgewater, New Jersey


The Sr Supplier Quality Auditor will assess the level of compliance of Valeant Pharmaceutical’s External Manufacturers with applicable cGMP and regulatory standards (e.g. 21 CFR parts 11, 58, 201-211, 820, 111, ISO 13485, ISO 9001, ISO 17025, ICH Q7) as well as Valeant’s quality standards.


Schedule, plan, execute, report, follow-up and close supplier audits (GMP, GLP, GCP)

Support preparation of annual Regional Supplier Audit Schedule

Prepare and report supplier audit metrics

Monitor and track supplier audit corrective action plans

Member of the Technical Auditing Committee and sub-teams

Develop and enhance Supplier Quality Audit Systems to reduce risk and increase compliance

Conduct Regional Compliance audits

Participate in Good Clinical Practice audits

Conduct For Cause Audits

Monitoring FDA audits and other regulatory actions regarding suppliers

Scope of position:

This position will require travel of 20 weeks or greater. Support Valeant US Region External Manufacturer annual audit schedule.

Conduct company audits of External Manufacturers with critical compliance and quality risks (i.e For Cause)

Responsible for Supplier Quality Management of limited Regional Service Providers such as Stability Labs and other services.

Key relationships:

Internal customers include supplier quality managers, engineers, Regulatory Affairs, Pharmacovigilence, R&D, GPSS ,Supply Chain

External customers include suppliers of products and services for pharma, devices and consumer


BS Degree in a scientific/technical discipline (Chemistry, Microbiology, Engineering)

Certified Quality Auditor (ASQ or other)

Extensive training in Quality Assurance concepts and applications including Internal Auditing, Supplier Auditing, Quality Engineering, Sterility Assurance, Statistics. Basically well rounded in the science of QA.

Excellent writing skills.


Minimum of 5 years of experience in FDA regulated industries (pharmaceuticals and medical device) with 5 years in a cGMP audit role. Prefer a person which has both pharmaceutical and device experience.

Working knowledge of 21 CFR 11, 210, 211, 820, 111, ICH, ISO 13485

**Total of 3 positions that can be based at any of the locations listed in the requistion

Job ID 7675

Location US - NJ - Bridgewater

US - MO - St. Louis

US - NY - Rochester

US - SC - Greenville

US - FL - Tampa South

Category R&D

Pos. Type Full Time