We are currently looking for a QC Analyst to join a leading pharmaceutical company based in the Hertfordshire area. As the QC Analyst, you will be responsible for ensuring the highest standards of quality control within the Pharmaceutical Development department.
Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows:
1. Carry out the Quality Control of raw materials, bulk, and finished products using HPLC, GC, and wet chemical techniques in accordance with relevant authorised documentation.
2. Perform swabbing and analysis of samples for cleaning verification of the pilot production facility.
3. Take equal part in the overall running of the laboratory, including equipment maintenance, calibration of apparatus, and other general duties such as solvent disposal.
4. Perform manual and automated tests and assays in accordance with GMP to a high level of accuracy and precision and operate associated analytical equipment.
To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history:
1. Relevant degree in a chemistry-based discipline.
2. Proven industry experience in an analytical testing role, preferably in a GMP environment.
3. A working knowledge and practical experience with HPLC and GC analysis.
Key Words: /QC Analyst/ /Quality Control/ /Pharmaceutical/ /HPLC/ /GC/ /GMP/ /Analytical Testing/ /Chemistry/ /Laboratory/ /PDS/
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows:
1. Carry out the Quality Control of raw materials, bulk, and finished products using HPLC, GC, and wet chemical techniques in accordance with relevant authorised documentation.
2. Perform swabbing and analysis of samples for cleaning verification of the pilot production facility.
3. Take equal part in the overall running of the laboratory, including equipment maintenance, calibration of apparatus, and other general duties such as solvent disposal.
4. Perform manual and automated tests and assays in accordance with GMP to a high level of accuracy and precision and operate associated analytical equipment.
To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history:
1. Relevant degree in a chemistry-based discipline.
2. Proven industry experience in an analytical testing role, preferably in a GMP environment.
3. A working knowledge and practical experience with HPLC and GC analysis.
Key Words: /QC Analyst/ /Quality Control/ /Pharmaceutical/ /HPLC/ /GC/ /GMP/ /Analytical Testing/ /Chemistry/ /Laboratory/ /PDS/
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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