Review/Release II

$500.00 Sign-on- Bonus!!

Join our Team!

Our number one commitment is to our employees happiness, safety, and security. At our facility, our employees have the opportunity to work in a unique and fun environment, where they can grow their skills and gain valuable experience. We offer a comprehensive employee benefits package, including health insurance, paid time off, paid holidays, 401K with 4% match & life insurance. Our Team Members make us who we are. They are the brightest minds bringing the boldest ideas to life every day.

We will build a reputation for reliability, integrity and honor.

Position Summary

The Quality Assurance Review Release II 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.

• 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.
• Track and monitor department KPIs to ensure that items are being released in a timely manner.
• Ensure records are GMP-compliant as required by SOPs, methods, or regulations.
• Ensure GDP is followed on all applicable batch documentation.
• Have a full understanding for the QA Review/Release I job responsibilities and be a leader/ trainer for any QA Review/Release I positions.
• 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.

• 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.

• 3 or more years prior work experience in Consumer-Packaged Goods (CPG), food, pharmaceutical, or manufacturing industry (can be substituted with education or applicable certifications).
• Experience with batch documentation in a cGMP environment is a plus.

• Must be able to climb stairs and sit for long periods of time.
• Move about inside the office to access file cabinets, office machinery, etc.

Qualifications