Jobiglo

No results.

Quality Assurance - Delegate Qualified Person

lilly · Mont Saint Guibert

New
Senior 67,500 - 99,000 EUR/year 🇬🇧 English
EU GMP GDP CAPA

Job description

About the role

Lilly is hiring a Delegate Qualified Person (QP) for its ELECTS QA and QP team in Belgium. The role covers QP tasks, PR&D QA duties and, where applicable, the final China release, working with the CSD, PR&D, the Global Quality Development Unit, Business Partners, CPs and Regulatory Affairs. It is a full-time position.

Key responsibilities

  • Delegate QP tasks such as EP batch release, QP certification of FING material received at the EU Hub, approval of deviations, change controls, study/country additions, retest date extensions, complaints, redistribution and supply chain mapping records, and EU GMP equivalency confirmations
  • Ensure clinical trial materials comply with EU and Belgian regulatory requirements and GMPs, and inform management of quality events that could affect product quality and compliance
  • PR&D QA: take part in regulatory inspections, external audits of partners and audit readiness, ensure CAPA are in place and followed, manage retention and reference samples, and support collaborations, alliances and Expanded Access programs
  • Perform the final China release where applicable, in line with the minimum experience requirement
  • Follow health, safety and environmental requirements and maintain confidentiality

Required profile

  • Scientific Master's degree in Pharmacy, Qualified Person
  • Several years of experience in QA-QP tasks in the pharmaceutical environment
  • Minimum 5 years of practical experience in drug R&D, production or quality management, with at least 1 year in drug quality management (for China release)

Required skills

  • Thorough knowledge of EU and Belgian regulatory requirements, EU GMP/GDP and Lilly quality standards for clinical trial materials
  • Knowledge of quality systems for deviations, change controls, complaints and CAPA
  • Ability to perform QP certification and batch release decisions, and to audit and approve quality documentation
  • Excellent written and verbal English, with the ability to escalate critical quality and regulatory issues

What we offer

  • Anticipated wage of EUR 67,500 - 99,000, depending on education, experience, skills and location
  • Possible company bonus for full-time equivalent employees
  • Benefits including pension plan, vacation, healthcare, flexible benefits, life insurance and well-being programs

Questions fréquentes

Le salaire proposé pour ce poste est de 68-99k EUR par an. Le détail figure dans l'annonce.
Cliquez sur "Postuler maintenant" en haut de la page. Vous pouvez importer votre CV en 1 clic — Jobiglo extrait automatiquement vos informations et postule pour vous.
Source : ats:workday

Why are you reporting this job?

Thank you for your report. We will review this job.

Explore further

Salaries, guides and searches in Belgium.

Apply in 30 seconds

Enter your email to apply. An account will be created automatically.

Apply now →

By continuing, you accept our terms of use.

Already have an account? Login

A question about this job?

Ask it here: you will get the full job summary by e-mail, right away.

Published 11 hours ago

Expires 1 month from now

6 views · 0 interested

Boost your chances

Upload your CV — we will match you with relevant openings.

Analyzing your CV...

lilly

Mont Saint Guibert