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PMQC Analyst

SRG
Posted 5 days ago, valid for 20 days
Location

Barnard Castle, Durham DL12 9EB, England

Salary

£19.83 per hour

Contract type

Part Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The PMQC Analyst position is located in Barnard Castle, UK, offering a salary of £19.83 per hour on a 9-month contract.
  • Candidates should possess a relevant science degree, such as in Chemistry or Pharmaceutical Sciences, and ideally have experience in a GMP environment.
  • The role involves adhering to Standard Operating Procedures, ensuring compliance with Good Manufacturing Practices, and participating in Continuous Improvement activities.
  • Applicants should be proficient in using laboratory instruments and analytical techniques, as well as in problem-solving and troubleshooting.
  • GMP experience is essential for this position, making it suitable for both recent graduates and those with prior industrial chemistry lab experience.

Job Title: PMQC Analyst

Location: Barnard Castle, UK

Salary: £19.83 per hour

contract: 9 months

Are you a chemistry graduate looking for your first role in industry? Or do you already have a background in an industrial chemistry lab but would like to develop your skills further in a GMP environment?

This client are a world-leading pharmaceutical organisation located in Barnard Castle with a vacancy for a PMQC Analyst.

Responsibilities:

  • To work as a flexible and motivated member of the team.
  • To follow all Standard Operating Procedures (SOPs) and/or Standard Work Instructions (SWI) applicable, and in which the individual has been trained.
  • To act, at all times, in compliance with Good Manufacturing Practices (GMP) and to report any quality issues.
  • To act in a safe manner, always (in compliance with the Health & Safety at Work Act, and all other relevant legislation) and to use GSK safety reporting systems to highlight potential hazards.
  • To remain up to date with all training requirements (both 'classroom' courses and computer- based training through the 'My Learning' internal platform).
  • To take part in Continuous Improvement (CI) activities to highlight improvements to equipment and processes.
  • To take part in Root Cause Analysis (RCA) and Corrective and Preventative Action (CAPA) processes.
  • Testing and performing batch usage decisions on incoming deliveries prior to production use.
  • Writing and checking of methods and SOPs.
  • Schedule activities and workload within the department.
  • To give support to other team members.
  • Vendor rejections

Requirements:

  • Relevant Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent.
  • Is proficient in the use of numerous Laboratory instruments, software packages and other analytical techniques (E.g. Empower 3).
  • Is proficient in problem solving and may have expertise in troubleshooting analytical equipment.
  • GMP experience is essential.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.