Quality Operations Associate- Contract - Philadelphia, PA
Proclinical is seeking a Quality Operations Associate who will play a crucial role in ensuring compliance with cGMPs and facility procedures.
Primary Responsibilities:
The successful candidate will collaborate with various functional groups, such as Manufacturing, Quality Control, and Document Control, to identify and report any events such as errors, deficiencies, discrepancies, deviations, and other observations. This role involves reviewing batch records and related production documentation, ensuring all identified issues are resolved before product disposition. The Quality Operations Associate will also be responsible for the disposition of incoming raw materials and maintaining Quality Metrics.
Skills & Requirements:
Bachelor's Degree in Science, Engineering, or a related technical discipline or equivalent industry experience.At least 1- 3 years' experience in a regulated industry.Knowledge of cGMP regulations.Ability to work in an aseptic processing environment.Strong administrative skills including use of Microsoft Word, Excel, and PowerPoint.Attention to detail.Knowledge of QMS systems is a plus.
The Quality Operations Associate's responsibilities will be:
Compensation: USD 35 - 38 per hour
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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