Biochemical QC Supervisor

Philogen S.p.A.; Siena; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

Philogen S.p.A., leader en développement de thérapies anti-tumorales, recherche un Quality Control Supervisor engagé. Ce poste inclut la supervision des fonctions de laboratoire, la gestion des contrôles qualité de matières premières et la conformité avec les normes GMP. Le candidat idéal aura un solide bagage scientifique et des compétences avérées en chromatographie.

Servizi

Environnement dynamique

Contrat permanent

Competenze

• Bonne connaissance des GMP requise.
• Expérience avec la chromatographie et les tests biochimiques.
• Capacité à valider des méthodes selon les normes édictées.

Mansioni

• Superviser les fonctions du laboratoire biochimique et la documentation.
• Assurer la conformité aux normes de qualité et GMP.
• Favoriser l'amélioration continue dans les opérations de QC.

Conoscenze

Connaissance des GMP

Techniques chromatographiques

Analyses biochimiques

Anglais

Formazione

Formation scientifique pertinente

Descrizione del lavoro

Direct message the job poster from Philogen S.p.A.

Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is looking for a highly motivated and qualified Biochemical Quality Control Supervisor who will report directly to the Quality Control Manager.

In particular the successful candidate will be Responsible for:

• Biochemical laboratory functions and the corresponding documentation to support the timely disposition of product.
• Overall Quality control disposition of incoming materials, in process samples and finished products.
• Analytical method set-up, validation, trasfer and writing reports.
• Insuring compliance of laboratory procedures and practices with Philogen Quality standards and with GMP regulations.
• Support day to day scheduling activities closely with the QC manager.
• Facilitating continuous improvement in QC day to day operations and general systems and will actively support achievement of plant goals. Coaching and developing QC colleagues to achieving high performance.
• Supporting laboratory colleagues in all aspects of their work to achieve the completion of tests and/or investigations in a timely manner as well as maintaining an updated knowledge base in the technical, operations, company policy and regulatory fields.
• Promote the technological innovation, scientific understanding and best practies, to design an integrated analytical development strategy, within the QC manager.

The ideal candidate should have:

• A good scientific background
• Comprehensive knowledge of GMP
• Knowledge on chromatographic technics as Size Exclusion Chromatography/ Cation Exchange by HPLC and common biological test (e.g. Bioactivity, E.L.I.S.A.)
• Chemical-physical analytical determinations
• Knowledge of method validation and trasfer, in compliance with EP/USP.
• Good English knowledge.

We offer:

• A dynamic environment.
• A permanent contract with a salary proportional to the experience level of the successful candidate.
• to the experience level of the successful candidate.

Job location:

We invite interested candidates to submit their applications expressly authorizing the processing of personal data in accordance with Legislative Decree 196/2003. Our recruitment adheres to the provisions of Legislative Decree 198/2006, and we welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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