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CK Group, a leading provider of scientific, clinical, and technical services, is seeking a highly skilled Shift Quality Control Analyst to join their team in a Quality Control Laboratory. The successful candidate will work on a permanent basis, contributing to the development and manufacture of veterinary products for a globally recognized organization.
This is an excellent opportunity for career advancement for chemists who are eager to gain experience in a renowned organization. The Quality Control Analyst will play a crucial role in ensuring the quality of pharmaceutical raw materials, intermediates, and final products.
Key Responsibilities:
- Perform quality control analysis on pharmaceutical raw materials, intermediates, and final products, adhering to analytical methods and cGMP principles.
- Operate a range of analytical instrumentation, including HPLC and GC, to ensure accurate and reliable results.
- Develop and validate new and existing analytical methods, contributing to the improvement of quality control processes.
- Collaborate with the team to maintain a safe and healthy working environment, adhering to health and safety protocols.
Requirements:
- Degree in a Chemistry-related subject or relevant industrial experience.
- At least 3-5 years of experience in industry using HPLC and GC.
- Proven experience working in a Quality Control laboratory, with a strong understanding of cGMP requirements.
- Familiarity with health and safety protocols in a working laboratory environment.
CK Group- Science, Clinical and Technical is committed to providing a supportive and challenging work environment. If you are a motivated and experienced chemist looking to advance your career, please submit your application.