Quality Control Associate
- Contract
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Quality Control Associate with a global biotechnology company located in Durham, NC. Successful candidate will sample and inspect, test support, robust and compliant cGMP documentation practices. Candidate must also have a fundamental understanding of the cGMP compliance and able to apply it in their daily support functions.
Job Responsibilities:
- Sample and inspect raw materials.
- Perform routine release testing of Raw Materials using Raman spectrometer, appearance, pH and osmolality per compendia.
- Responsible for adherence to all cGMP requirements.
- Interactions/communication with Quality management. The incumbent should be able to work effectively within the group.
Skills and Requirements:
- Possess demonstrated technical ability regarding fundamental laboratory techniques and analytical methodology.
- Understanding of scientific principle, ability to communicate with peers and management; GMP/GDP experience.
- Basic understanding of FDA/EMA regulations.
- Effective organizational skills.
- Ability to coordinate multiple activities in parallel to meet required timelines.
- Ability to work independently and as part of a team.
- Demonstrated problem solving skills.
- Solid working knowledge of operations/quality systems utilized in QC operations/support teams (eg; strong test method/scientific base).
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Zachary Hines at (+1) 215-531-6914 or upload your resume on our website - www.proclinical.com.
A full job description is available on request.
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.
#LI-ZH1
#Compliance/Quality
Related jobs
Highly Competitive
Berne, Switzerland
Ready to use your FMEA and GMP knowledge to identify risks, strengthen processes, and make a meaningful impact in a highly regulated industry?
Highly Competitive
Paris, France
Notre client recherche un Coordinateur QHSE Prestataires pour rejoindre leur équipe et intervenir sur le site de l'un de leurs clients majeurs en pharmaceutique.
€40000 - €75000 per annum
Normandy, France
Vous parlez couramment LEAN (5S, SMED et Kaizen)? Vous avez déjà transformé un atelier plus vite qu'un café ne refroidit ? On a un poste pour vous?
Highly Competitive
Basel, Switzerland
Join a high performing CMO where your quality expertise keeps site operations running with precision, efficiency, and flawless coordination.
US$20 - US$24 per hour + Highly Competitive Salary
Hoover, USA
Ready to grow your career in sterile compounding? Looking to join a thriving pharmaceutical operation and help deliver exceptional standards of quality and compliance.
Highly Competitive
Philadelphia, USA
Play a crucial role in advancing life-changing cell and gene therapies by ensuring GMP production environments remain audit-ready and contamination-free.
Highly Competitive
Bristol, USA
Join a team transforming the future of medicine through cutting-edge bioconjugation and gene therapy manufacturing.