SonicJobs Logo
Left arrow iconBack to search

Head of Quality

X4 Life Sciences
Posted 7 hours ago, valid for 6 days
Location

Stevenage, Hertfordshire SG1 2AX, England

Salary

£48,000 - £57,600 per annum

info
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

info
  • An exciting opportunity has arisen for the position of Head of Quality at a growing generics pharmaceutical manufacturer in Hertfordshire.
  • The role requires a minimum of 5 years of experience in Quality Assurance within a manufacturing site, along with previous leadership experience in the pharmaceutical industry.
  • Key responsibilities include overseeing the quality management system, ensuring compliance with registered MA requirements, and managing third-party audits.
  • The successful candidate will also be responsible for hosting MHRA inspections and maintaining compliance with GMP and product licenses.
  • Salary details for this position are not specified, but candidates should possess a bachelor's or associate degree and extensive knowledge of GxP environments.

Exciting opportunity: Head of Quality for a growing generics pharmaceutical manufacturer.

If you are a seasoned Quality professional, based in or around Hertfordshire, with leadership experience in the pharmaceutical industry, this role might be for you!

Your Responsibilities:

  • Responsible to oversee and continually review the quality management system to ensure that improvements are identified and that any deficiencies are addressed at their root cause and appropriate procedures are developed and fully implemented.
  • Verify and ensure that the products are manufactured, packed and tested to the requirements of registered MA.
  • Responsible to review the third-party audit reports for APIs and packaging materials. Responsible for the review of annual product quality reviews.
  • Ensuring complaints and adverse incidents are accurately recorded and addressed in a thorough and timely manner in accordance with the company QMS.
  • Responsible for hosting MHRA inspections, writing the response reports and to liaise with the Medicines Inspectorate to ensure that the Company conforms to the requirements of GMP and the Manufacturing and Product Licenses.
  • Develop, manage and maintain the company's device family technical files and product specific design dossiers ensuring compliance with the relevant regulations.
  • Remain up to date with impending changes and developments regarding regulatory and compliance requirements as well as evolving best practices in compliance control.
  • To approve specifications, sampling instructions, test methods, and QC procedures, including amendments.
  • To approve and monitor suppliers of raw materials and packaging components.

Your experince, skills and qualifications:

  • A bachelors or associate degree.
  • A minimum of 5 years experince in the Quality Assurance at a manufacturing site
  • Previous experince in a leadership role.
  • Extensive Pharmaceutical Industry experince with hands on experince in development/quality in a GxP environment.

If this sounds like the perfect opportunity for you or someone you know, please share your CV at !

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.