SonicJobs Logo
Login
Left arrow iconBack to search

Senior Process Quality Excellence Specialist

ARM
Posted 11 days ago, valid for 5 days
Location

Slough, Berkshire SL11XY, England

Salary

£48,000 - £57,600 per year

info
Contract type

Full Time

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • The position is for a Senior Process Quality Excellence Specialist with a leading multinational biopharmaceutical company based in Berkshire.
  • Candidates must have over 8 years of pharmaceutical experience, particularly in global quality assurance or clinical development, along with 2+ years of experience in SOP writing.
  • The role involves supporting the Head of Process Quality Excellence in developing clinical quality systems and ensuring compliance with GCP, GLP, and PV regulations.
  • This is a contract position for 12 months, offered on a hybrid basis and is classified as inside IR35.
  • The salary for this position is not specified in the job description.

Are you an experienced Quality Assurance professional? Do you have a background in a Pharmaceutical or Clinical Development setting? If so, this could be the perfect opportunity for you!

We are recruiting for a Senior Process Quality Excellence Specialist to join a leading multinational biopharmaceutical client based in Berkshire.

The successful candidate will support the Head of Process Quality Excellence in developing and maintaining its clinical quality systems/procedures and ensuring quality and compliance risks are appropriately identified and mitigated.

Candidates will need experience and focus on GCP, GLP and PV regulations and guidance.

This is a contract position, inside IR35, offered initially for 12 months on a hybrid basis.

Responsibilities:

  • Support the Head with quality and compliance infrastructure development, assist with creation/revision of appropriate quality and compliance policies, SOPs, processes, and best practices as needed.
  • Work in collaboration with Global Quality, Patient Safety, Regulatory Affairs, strategic partners, and other stakeholders to ensure compliance with International Council for Harmonization of Technical Requirements for ICH, GCP, GLP, PV and relevant local and international regulations and to ensure inspection readiness.
  • Lead and drive inspection readiness activities across functions working closely with the relevant inspection teams.
  • Participate in audit and inspection planning with global quality.
  • Represent or ensure representation including preparation during audits/inspections / on-site by internal and external parties.
  • Support staff with audit/inspection responses, where required.

Requirements:

  • 8+ years of pharmaceutical experience, preferably in a global quality assurance or a clinical development setting.
  • In depth experience of GCP and GVP, including hands on experience in global GCP audits and/or inspections.
  • 2+ years of experience in SOP writing essential.

Disclaimer:

This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission. Where the role is marked as Outside IR35 in the advertisement this is subject to receipt of a final Status Determination Statement from the end Client and may be subject to change.

Apply now in a few quick clicks

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.