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Risk Assessment Coordinator

SRG
Posted 7 hours ago, valid for 17 days
Location

Golcar, West Yorkshire HD7, England

Salary

£30,000 - £36,000 per annum

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Contract type

Part Time

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Sonic Summary

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  • The Risk Assessment Coordinator position is a 6-9 month fixed-term contract based in West Yorkshire with a rapidly growing pharmaceutical producer.
  • The role involves managing and collating risk assessment and testing data to ensure the quality and safety of materials used in medicine production.
  • Candidates should have a relevant scientific degree or equivalent qualification, along with previous experience in a GMP-regulated QC or laboratory environment.
  • The position offers flexible working hours and requires strong administrative, data management skills, and attention to detail.
  • Salary details are not specified, but applicants must be available to start at short notice and have the right to work in the UK.

Title: Risk Assessment Coordinator

Location: West Yorkshire

6-9 Month Fixed-Term contract

SRG are recruiting for a Risk Assessment Coordinator to be based with a rapidly growing pharmaceutical producer in West Yorkshire. Manufacturing numerous household brands found in homes across the country, they also produce specialist prescription products for the NHS.

This position will play an essential part in ensuring that the materials used to produce medicines & pharmaceuticals are of the highest quality & safe to use.

The role

Working alongside the QC team, you will be responsible for managing and collating Risk assessment & testing data.

Key duties will include:

  • Collating & managing Raw Material safety information, Risk assessments and supplier information.
  • Work collaboratively with the QC team to support ongoing quality initiatives.
  • Maintain and organise documentation in accordance with GMP and company procedures
  • Ensure all activities are carried out in line with GMP & ISO quality standards.

Working Hours: 38 hours per week

Flexible hours are available.

Requirements:

  • A degree or similar qualification or experience in a relevant subject.
  • A relevant scientific degree or equivalent similar qualification.
  • Previous experience working within a GMP-regulated QC or laboratory environment is highly desirable.
  • Strong administrative and data management skills, with proficiency in MS Office and other relevant systems.
  • Excellent attention to detail and the ability to work independently and as part of a team.
  • Must be available to start at short notice.
  • Applicants must have the right to work in the UK - sponsorship is not available for this position.

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

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