Valeant Pharmaceuticals

Compliance Specialist - APR

US-FL-Tampa
Job ID
9207
Category
R&D
Pos. Type
Full Time

Overview

Responsible for compiling, reviewing, tracking and maintaining Annual Product Reviews (APRs).   Responsible for performing APRs related to finished product, raw materials/components and customer complaints.  Serves as back up for technical product complaint investigation process.  Serves as back-up for incoming inspection disposition.

Responsibilities

Responsible for:

  1. Compiles, reviews, tracks and maintains APRs.
  2. Performs APRs related to finished product, raw

            materials/components and customer complaints.

  1. Serves as a backup by conducting the disposition of incoming

            receipts which encompasses raw materials, filling components and  

            secondary packaging.

  1. Serves as back up for technical product complaint investigation

            process.

  1. Supports generation of data for monthly department QPIs.

6.         Any other duties as assigned.

Qualifications

BS degree in Natural Sciences, Engineering or related field.

4+ years of pharmaceutical/FDA regulated facility or related field required. Ability to work independently. Ability to communicate and work well with others. Familiar with component and label testing techniques. Knowledge of sampling plans (e.g. Mil standard) and GxP compliance requirements. Computer knowledge ; knowledge of ERPLx preferred but not a requirement. Six Sigma training and/or Minitab training preferred.

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