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Risk Assessment Coordinator

SRG
Posted 4 hours ago, valid for 17 days
Location

Huddersfield, West Yorkshire HD7 5QH, England

Contract type

Full 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 position of Risk Assessment Coordinator is available for a 6-9 month fixed-term contract 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 pharmaceuticals.
  • Candidates are required to have a relevant scientific degree or equivalent qualification, along with previous experience in a GMP-regulated QC or laboratory environment.
  • Strong administrative and data management skills are necessary, and proficiency in MS Office is required, with a salary of £30,000 to £35,000 per annum.
  • Applicants must have the right to work in the UK and should be available to start at short notice.

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.

Apply now in a few quick clicks

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.