Quality Review/Release I

Beauty Manufacturing Solutions Corp•Coppell, TX

About The Position

The Quality Compliance Review/Release I position is responsible for the day-to-day review of bulk and/or Finished Goods (FG) batch record documentation and the release of bulk and FG, ensuring they meet quality standards set by management, customers, and regulatory requirements. The role works cross-functionally with Production and Manufacturing to ensure specifications are met. The position requires strong attention to detail, situational awareness, and the ability to ensure quality requirements are fulfilled. The position also supports compliance with SOPs, GMP, and GDP requirements; contributes to Annual Product Reviews of OTC products; enters Production KPI information as appropriate; and leads special projects as assigned. The role may require flexible schedules, including overtime, night shifts, and weekend shifts.

Requirements

Detail-oriented.
Good verbal and written communication skills and computer literacy, including MS Office.
Good math proficiency.
Organized and analytical.
Able to work flexible schedules, including overtime, night shifts, and weekend shifts.
Two or more years of prior work experience in the Consumer Packaged Goods (CPG), food, pharmaceutical, or manufacturing industry; experience may be substituted with education or applicable certifications.
Able to sit, balance, climb, stand, bend, squat, squeeze, kneel, turn, crouch, and stoop repeatedly.
Physically able to lift 50 pounds repeatedly.
Able to tolerate frequent exposure to varying temperatures, loud noises, heavy machinery, fumes, airborne particles, moving mechanical parts, electrical current, chemicals, and vibrations.
Able to use a computer screen for prolonged periods.

Nice To Haves

Experience with batch documentation in a cGMP environment.
Bilingual in English and Spanish.

Responsibilities

Ensure SOPs are followed to meet and exceed quality standards set forth in specifications.
Collaborate and communicate with upper management and Operations.
Review batch documentation to ensure appropriate processes are being followed and documented.
Release batches in a highly regulated environment.
Review documentation and have corrections made by the personnel who generated the documentation non-conformance.
Enter Production KPI information, as appropriate.
Ensure records are GMP-compliant as required by SOPs, methods, or regulations.
Ensure GDP is followed on all applicable batch documentation.
Support the company mission, values, and standards of ethics and integrity by incorporating these into the development and implementation of business plans.
Participate in the generation of Annual Product Reviews (APRs) of OTC products.
Own and lead special projects as assigned.
Perform all other assigned duties as required by Quality Management.