Quality Release & Compliance Specialist

Beauty Manufacturing Solutions Corp

Coppell (TX)

On-site

USD 52,000 - 76,000

Full time

6 days ago
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Job summary

Beauty Manufacturing Solutions Corp in Coppell, TX is seeking a Quality Compliance Review/Release I to join our small team. The role focuses on day-to-day batch record review and release to meet quality, regulatory, and GMP standards, collaborating with Production to ensure specifications are met.

The ideal candidate is detail-oriented, adaptable, and a strong communicator, able to follow SOPs and maintain GMP/GDP-compliant records.

Qualifications

  • 2+ years in CPG, food, pharmaceutical, or manufacturing.
  • 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.
  • 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.

Skills

Detail oriented
Verbal and written communication
Organized and analytical
Flexible schedule

Tools

MS Office

Job description

Beauty Manufacturing Solutions Corp in Coppell, TX is seeking a Quality Compliance Review/Release I to join our small team. The role focuses on day-to-day batch record review and release to meet quality, regulatory, and GMP standards, collaborating with Production to ensure specifications are met.

The ideal candidate is detail-oriented, adaptable, and a strong communicator, able to follow SOPs and maintain GMP/GDP-compliant records.

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