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    {"title": "QC Chemist Role", "content": "Key ResponsibilitiesTo test routine production & stability samples supplied from the site Value Streams and meet testing lead-time targets.Calibrate & maintain analytical equipment.Carry out qualitative & quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques...

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    Worthing, West Sussex, United Kingdom CK Group Full time

    {"title": "QC Chemist Role", "content": "Key ResponsibilitiesTo test routine production & stability samples supplied from the site Value Streams and meet testing lead-time targets.Calibrate & maintain analytical equipment.Carry out qualitative & quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques...


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    QC Chemist Job DescriptionCK Group is seeking a highly skilled QC Chemist to join their team at a pharmaceutical company in Worthing, UK. This is a contract-based position for 11 months, offering a competitive hourly rate of up to £14.45.Key Responsibilities:Conduct routine production and stability sample testing, ensuring timely completion and meeting...

QC Analyst

4 months ago


Worthing, United Kingdom CY Partners Full time

CY Partners have an exciting new opportunity, for you, as a QC Analyst specializing in Analytical Chemistry. If you're passionate about maintaining the highest quality standards in pharmaceuticals this is the perfect opportunity for you.This role is an initial 6 month contract role, with good scope for further. You will work on a rota of morning and afternoon shifts (no night shift).Role Responsibilities:Perform routine analytical testing on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, and dissolution testing.Collaborate with cross-functional teams to investigate and resolve any discrepancies.Maintain and calibrate analytical instruments to guarantee their accuracy and reliability.Generate and review analytical data, ensuring strict compliance with GMP guidelines and internal quality standards.Contribute to the continuous improvement of laboratory procedures and protocols.Key Requirements:Bachelor's degree in Chemistry or a related field (or equivalent).Strong expertise in analytical techniques such as HPLC, GC, and UV-Vis.Knowledge of GMP regulatory requirements.Detail-oriented with excellent problem-solving skills.Effective communication and teamwork abilities