1st Shift Review/Release I

BEAUTY MANUFACTURING SOLUTIONS CORP•Coppell, TX

2d•Onsite

About The Position

The Quality Compliance Review/Release I position will be responsible for the day-to-day review of bulk and/or Finished Goods (FG) batch record documentation and release of bulk and FG to ensure they meet the high-quality standards set by management, customers, and regulatory requirements. They will work cross-functionally with Production and Manufacturing to ensure that specifications are being met. This position must be detail-oriented. The ideal candidate will demonstrate strong attention to detail, situational awareness, and the ability to ensure that the quality requirements are fulfilled, as required.

Requirements

Detail oriented.
Good verbal and written communication and computer literacy (MS Office) required.
Good math proficiency.
Organized and analytical.
Must be able to work flexible schedules including overtime, nightshift, and weekend shifts.
2 or more years prior work experience in Consumer Packaged Goods (CPG), food, pharmaceutical, or manufacturing industry (can be substituted with education or applicable certifications).

Nice To Haves

Experience with batch documentation in a cGMP environment is a plus.
Bilingual in English/Spanish a plus.

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 of batches in a highly-regulated environment.
Review all 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.