Similar posts
Quality Operations Associate
- Contract
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
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:
- Ensure compliance to cGMPs and facility procedures.
- Collaborate with functional groups to identify and report any events.
- Review batch records and related production documentation.
- Resolve all identified issues before product disposition.
- Disposition incoming raw materials.
- Maintain and report on Quality Metrics.
- Initiate and participate in standard operating procedure (SOP) revisions.
- Perform other tasks as assigned.
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.
INDCQA
Related jobs
Highly Competitive Salary
Frankfurt am Main (60318), Germany
Leiter Methodenentwicklung (m/w/d)** | Dauerhaft | Biowissenschaften | Deutschland (Frankfurt am Main)
US$18 - US$22 per hour
Durham, USA
Are you looking to make an impact with your innovation? We are working with a well-established pharmaceutical company to recruit for a dedicated document controller.
Highly Competitive Salary
Basel, Switzerland
Proclinical is seeking a Supplier Lifecycle Management Specialist to support global vendor change notifications and ensure seamless coordination across multiple sites.
Highly Competitive
Visp, Switzerland
Step into a pivotal role at a global CMO and help shape the future of healthcare manufacturing.
Highly Competitive
Visp, Schweiz
Join a cutting-edge pharmaceutical team where your precision and passion for quality will help shape the future of life-saving medicines!
Highly Competitive
King of Prussia, USA
Proclinical is seeking a QC Environmental Monitoring Expert to support quality control operations in a GMP-regulated environment.
Highly Competitive
Jena, Germany
Proclinical sucht einen Abteilungsleiter (m/w/d) für den Bereich Qualifizierung zur Verstärkung des Teams unseres Kunden in Deutschland für eine Festanstellung.