QC Supervisor

Overview: Provide supervision of Chemists performing routine chemical analysis accurate, cGMP compliant testing of pharmaceutical raw materials, process intermediates, and finished products.

Maintains communication as to the status of work being performed with manager and interaction with other Departments.

Adheres to cGMP and Andrx SOPs.

Reports any OOS results encountered when testing.

Reports any deviations to a procedure before proceeding.Responsibilities:

Responsible for overall operation including Planning, Coordinating, Metrology, Technical Training, Method Transfers, and Method Improvements.

Plans, assigns, reviews, and supervises the work of others.
Consults with management on assignments work flow and quality assurance.

Coordinates OOS/OOT investigations with the Laboratory OOS Investigators.

Leads investigations, interprets results and recommends final disposition for related Out-of-Specification (OOS) results.

Ensures the quality of chemical and physical data is maintained.

Prepares and maintains Standard Operating Procedures, Standard Test Methods, and Specifications.

Devises and implements corrective and preventative action plans.

Ensures laboratory instruments are qualified, calibrated, maintained, and in good working order.

Interacts with instrument and laboratory supply vendors.

Recommends equipment and personnel needed for laboratory functions.

Increase Laboratory testing efficiency.

Assists with Method Transfers for Quality Control Laboratory.

Reviews and approves documentation and Release Laboratory test results.

Proficient in computer usage.Job Requirements
Qualifications:


Four-year degree in a Science discipline with at least 7 years of relevant work experience, minimum 3 years in a Supervisor capacity or equivalent.

Master’s Degree in a Science discipline with at least 5 years of relevant work experience, minimum 1 year in a Supervisor capacity or equivalent.

PhD with minimum of 1 year in a Supervisory capacity or equivalent.