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QP Biopharma

Michael Page
Closing date
1 Nov 2021

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Salary Band
Annual, £70,000 - £99,999
Contract Type
Full Time
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Global Life Science organisation

Job Description
  • Providing QP certification in compliance with regulatory requirements and if required, specific client technical agreements
  • Providing QP GMP declarations, including on site audits if required, in support of importation activities.
  • Provision of GMP training.
  • To provide information and training on the QP roles and responsibilities to FBS personnel.
  • Provide support to Business Development/Sales and Project Management at pre-contract stage to assess new contracts.
  • To maintain an up to date awareness of the regulatory issues affecting the clinical supplies process keeping relevant FBS colleagues informed where appropriate.
  • To provide technical advice and support in the preparation of Technical Agreements.
  • Support client and regulatory audits with QP input.
  • May be required to perform off site work where necessary.
  • Occasional travel as required.
The Successful Applicant
  • You must be an eligible Qualified Person (as per Article 49 of Directive 2001/83/EC) - we are open to someone who is newly qualified or more experienced
  • Biological experience or education - advantageous, not essential
  • Open to occasional national and international travel - preferred, not essential
  • Knowledge of the pharmaceutical product development process - desirable, not essential
What's on Offer
Competitive salary package and bonus

Ivan Gitardi

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Phone number
+44 1727 730 145
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