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Mgr-Quality Assurance

at L'Oreal USA in North Little Rock, Arkansas, United States

Job Description

The Quality Assurance Manager is responsible for establishing and implementing the Quality Management System in correspondence with the L'Oreal Quality System, guaranteeing implementation and follow-up on new or existing procedures, leads internal and external audits, and ISO quality certification. Responsible for managing the programs required for compliance to FDA regulation for drug products and DGO system requirements.
Educational, Mental, or Certification Requirements
BS Degree in a Science, or Engineering field, Masters preferred;
Minimum 5 years of experience in a Quality management role;
Ability to learn statistical processes and Standard Operating Procedures;
Requires the ability to meet deadlines, have good organizational skills and have the ability to work independently;
Requires ability for test design and interpretation of results;
Must have strong communication skills, presentation skills, writing skills;
General Job Duties
Responsibilities are not limited to the below listing:
The management and maintenance of the North Little Rock Plant Quality System: including preparation of formal procedures as required by the DGO, ISO and GMP, quality system documentation reviews (internal and external), reviews and approves internal documents, management of the EtQ document control system;
Develops and manages the training program regarding GMPs and the Quality System: trains selected personnel in audit techniques, prepares training material with Quality department and provides training for Good Manufacturing Practices (Preweigh, Manufacturing, Filling);
Assists with the internal and external audits of the facility: Perform audits, Coordinates and records documents requested by external auditors, documents audit activities for external auditors, ensures corrective measures are taken by the appropriate department in a timely manner;
Coordinates compliance to FDA regulations of drug products
Coordinates OTC Stability Program - ensures required OTC products are placed on long term stability each year and that samples are tested by appropriate labs and maintains records of all testing performed;
Ensures completion of Annual Product Review for OTC products - coordinates yearly physical and statistical evaluation of OTC products and maintains records of the review;
Reviews quality procedures for GMP requirements;
Coordinates and documents the annual validation of raw material tare weights in Flexnet;
Provides resources, guidance (formalization), and training for IQ/OQ validation activities in the plant: Works with UPs to identify equipment to be validated, reviews validation documents and studies;
Supports Document Control and Lot Dossier product release as needed;
Any other duties and projects as assigned.

If you require a reasonable accommodation to complete an application for a recognized disability under applicable law, please email . Please note this email will only respond to specific requests for assistance completing the application as a request for accommodation for a disability. All others will not be considered.

We are an Equal Opportunity Employer and take pride in a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.

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Job Posting: 3188902

Posted On: Jan 05, 2022

Updated On: Feb 04, 2022