Similar posts
Quality Control Associate
- Permanent
- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), Good Clinical Practice (GCP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is recruiting for a Quality Control Associate for a global biotechnology company located in Research Triangle Park, NC. As the QC Associate, you will support release and stability testing of finished products using analytical methods, as well as validation/transfer of analytical methods, and technical support of QC investigations. He/she must have the ability to work effectively independently, within a team framework, and across all business areas and levels of the organization.
Job Responsibilities:
- Performing release and stability testing for finished products, including timely review of data and maintaining records following cGMP documentation practices.
- Support for the execution of method validations, qualifications and transfers.
- Participation in laboratory improvement projects, and troubleshooting of analytical methods in collaboration with teams as appropriate.
- Maintenance of effective laboratory systems to ensure integrity of all laboratory results.
Skills and Requirements:
- Bachelor's Degree in Science (e.g., Biology, Chemistry, Biochemistry, Chemical/Biochemical Engineering, or related disciplines)
- 0-2 years of relevant experience with analytical testing methodology (HPLC, GC, UV-Vis, Karl Fischer)
- Demonstrated technical abilities
- Solid presentation, oral and written communication skills; ability to communicate with peers and management
- Effective organizational skills; ability to multi-task and coordinate multiple activities in parallel
- Demonstrated problem solving skills
- Demonstrated instrument/method troubleshooting skills.
- Knowledge of cGMP requirements
- Familiar with FDA/EMEA regulations and compliance
If you are having difficulty in applying or if you have any questions, please contact Nikki Ranieri at (+1) 215-531-5288 or n.ranieri@proclinical.com.
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-NR1
Related jobs
Highly Competitive
Basel, Schweiz
Are you ready to turn precision into progress and play a key role in shaping the future of pharmaceutical innovation?
Highly Competitive
London, England
Shape quality standards worldwide-be the voice of compliance.
Highly Competitive
Stein, Switzerland
Safeguard quality, shape compliance, and power the future of aseptic manufacturing.
Highly Competitive
Visp, Schweiz
Ensure precision and compliance-drive quality control excellence as our QC Scientist in Switzerland.
Highly Competitive
Holzminden, Germany
Proclinical sucht einen Qualitätssicherungsingenieur (m/w/d) für eine befristete Vertragsstelle in Deutschland.
Highly Competitive
Minneapolis, USA
Ensure quality, drive compliance-join us as a QC Analyst and keep standards at their peak.
Highly Competitive
Philadelphia, USA
Champion regulatory compliance and quality assurance in a pivotal QA Specialist III role.
US$190000.00 - US$200000.00 per annum
Houston, USA
Lead the charge in GMP excellence-drive quality, compliance, and commercial readiness as Director of QA Operations.