Quality, Value, Respect ________________________________________________________ Quality Specialist Crown Laboratories, Inc. in Johnson City is looking for a qualified individual to join our Quality Department.
The QA Specialist is responsible for performing Quality compliance activities on the plant floor and ensuring that all activities are in compliance with company and regulatory guidelines and procedures.
In addition, the QA Specialist is also responsible for assisting in activities directly related to batch release, and batch record and procedure review, revision and approval.
Main Accountabilities Perform audits/checks of manufacturing, filling and packaging processes to include QA weight checks, line clearance activities, record review and signoff, cleaning verification label verification and reconciliation verification.
Approve minor deviations on the operation floor.
Review and approve executed batch records for completeness and accuracy for batch release.
Verify and ensure compliance with regulatory and company procedures and guidelines.
Perform investigations as required. Assist in other quality related functions as requested, (sampling, component receipt and inspection, etc.)
Job Related Qualification/Skills Bachelor's degree in a scientific field preferred Minimum of 3-7 years' experience in the Pharmaceutical or regulated industry with prior experience in plant quality assurance.
Demonstrated knowledge of cGMPs, ICH and other regulatory requirements for the manufacture, testing and release of pharmaceutical products.
Strong proficiency in Microsoft Office suite of products, (Word, Excel, PowerPoint) Excellent verbal and written communication skills.
If you are interested in joining our team, please send your resume to email@example.com We offer a competitive benefits package including vacation, medical, dental, vision, short/long term disability and 401k w/match.
We are an Equal Opportunity Employer