Incoming Associate (Quality Control) - Pharmaceuticals Not right for you? We've got others

Lancaster, SC
October 7th 2021
Minimum Degree:
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We are looking for an Incoming Associate to follow current Good Manufacturing Practices (cGMP) and current Good Documentation Practices (cGDP) to record all procedures in a timely manner. The Associate will understand and follow Standard Operating Procedures (SOP) in all functions executed and report any deviations where necessary.


Roles and Responsibilities:


Minimum Requirements:  Proficient in computer work processing and Microsoft Office applications. Ability to lift (up to 50lbs or by team lift) and maneuver material up to 100 lbs. Good written and oral communication skills that enable them to communicate well with other QCIA's and other departments.


Education and Experience: Minimum of Associates in Arts (AA) or a combination of higher education and two years' experience in a regulated cGMP environment. Experience in a Quality environment is preferred.


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