QC Analyst role working standard days on a 6m FTC (fixed term contract) and paying up to £27,000 (DOE), plus a benefits package including a competitive pension, private healthcare plan, up to 15% performance related annual bonus, annual pay review, flexible working opportunity, 25.5 days annual leave plus bank holidays, income protection, business and personal travel insurance, life assurance up to 4x base salary, cycle to work scheme and more!
This QC Analyst (Quality Control) role is working with a globally leading pharmaceutical manufacturing company which is present in more than 20 countries world-wide and has over 20,000 employees globally. Taking this opportunity as QC Analyst would mean working for a leading global producer of API's (Active Pharmaceutical Ingredients). This role would include opportunities to advance your career, skillset, and education.
Responsibilities of the QC Analyst will include:
As the QC Analyst, you will conduct analysis of raw materials and finished products in line with established SOPs, ensuring accurate interpretation, documentation, and communication of analytical data.
Hold responsibility for performing second analyst data checks, routine calibrations, and ongoing monitoring of analytical instruments, including basic troubleshooting and maintenance.
You will prepare customer samples, standards, and all related documentation, maintaining up-to-date analytical databases and spreadsheets.
In charge of supporting laboratory operations through housekeeping, standard assessments, and document generation or review in compliance with quality requirements.
You will adhere to COSHH regulations and always maintain safe laboratory practices.
Lead basic troubleshooting and maintenance of analytical systems
To be successful in this position as QC Analyst :
You will hold an either a HNC/HND or a degree in a relevant Analytical, Chemical or Pharmaceutical subject.
Have an established technical Laboratory background including proven experience of GC (Gas Chromatography) and HPLC techniques.
Experience in dealing with analytical reports and instrumental trouble shooting on a GMP site is also essential.
Please apply directly for this QC Analyst role