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Qualified Person

Job LocationNorthumberland
EducationNot Mentioned
Salary75,000 - 95,000 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

Role OverviewWe are currently looking for a Site QP to join a global pharmaceutical manufacturing company based in Northumberland. As the Site QP you will act as the key contact for all QA and GMP issues on the manufacturing site including imports and the manufacturedproducts.Duties and Responsibilities

  1. You will act as the QP for release of products to market and be names on the companies license.
  2. You will ensure products are made in accordance with manufacturing licenses and equivalent marketing authorisations.
  3. As the Site QP you will ensure products, process and facilities comply with the suitable regulatory requirements and that they are aligned with company policies.
  4. You will provide support for customer visits and audits. You will also conduct internal audits and advise on corrective actions.
  5. You will conduct external audits of supplies vendors, contractors and service providers
  6. As the QP you will support QA Manufacturing, packaging and supply chain and also provide support to all business areas.
Experience and Education
  1. A number of years of industry experience working in pharmaceutical quality assurance.
  2. Eligibility to work as a Qualified Person is essential.
Pharmaceutical | Quality Assurance |QA | Manufacturing | GMP | MHRA | FDA | QP | Qualified Person |To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England andWales

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