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Qualified Person

SRG
Posted 10 days ago, valid for 14 days
Location

Huddersfield, West Yorkshire HD5 8XT

Salary

£45,000 - £54,000 per annum

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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 Qualified Person (QP) is available in Yorkshire with a permanent employment type and an attractive salary depending on experience.
  • The role involves guiding and advising team members, contributing to the company's GMP strategy and general QMS.
  • Key responsibilities include batch certification and release for licensed products, approval of QP declarations for license submissions, and reviewing third-party QA audit reports.
  • Candidates must have prior experience in a similar role and be familiar with EU Directive 2001/83/EC and relevant Human Medicines Regulations.
  • The job is offered by SRG, a leading recruitment company in the science and pharmaceutical sectors.

Title: Qualified Person (QP) Location: Yorkshire Employment Type: Permanent Salary: Attractive salary depending on experienceWe are currently working with a well-established pharmaceutical organisation specialising in generic pharmaceutical products, with a number of licensed medicines in the market. As the Qualified Person supporting all departments within the business, this position is responsible for guiding and advising all members of the team, contributing to the company GMP strategy and general QMS. The main duties and responsibilities will include:

The primary responsibilities of this role involve adhering to the following guidelines and policies:

  • Orange Guide, Part 1, Chapter 2 - Personnel.
  • Orange Guide, Annex 16 - Certification by a Qualified Person and Batch Release.
  • Human Medicines Regulations (as amended), SI 2012/1916, Schedule 7, Part 3.

As well as this, daily responsibilities include:

  • Batch certification and release for licensed products manufactured on site by the company, the CMO in third countries and for medical device and cosmetic products manufactured on site by the company.
  • Approval of QP Declaration for license submissions.
  • Review and approval of Third-Party QA audit reports.

The successful Qualified Person will require prior experience within this area of work, more specifically being highly familiar with EU Directive 2001/83/EC, Article 49 and Human Medicines Regulations (as amended), SI 2012/1916, Schedule 7, Part 1.

Interested? Or know someone who will be?SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you are interested in this role and require more information, please contact Elliott Howells on

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.