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Senior Quality Control Analyst

Famar Group

Milano

In loco

EUR 40.000 - 50.000

Tempo pieno

30+ giorni fa

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Descrizione del lavoro

Une entreprise leader dans le secteur pharmaceutique recherche un Scientifique en Contrôle Qualité pour son site à Baranzate. Ce poste clé nécessite une expertise en instrumentation analytique et une solide expérience en conformité avec les normes cGMP. Les candidats doivent avoir un diplôme dans un domaine pertinent et au moins cinq ans d'expérience. Le poste offre une opportunité de contribuer à des processus critiques de contrôle qualité au sein d'une équipe dynamique.

Competenze

  • Expérience professionnelle minimum de 5 ans dans l'industrie pharmaceutique.
  • Forte expérience dans les activités de validation analytique et les méthodes.
  • Bonnes compétences organisationnelles et de planification.

Mansioni

  • Effectuer des tests de matières premières, produits en cours et finis conformément aux procédures.
  • Optimiser les méthodes analytiques et assurer la validation méthodologique.
  • Participer aux audits internes et externes.

Conoscenze

HPLC
GC
IR
UV-Spectrophotometer
cGMP
Optimization des méthodes analytiques
Préparation de protocoles et rapports
Test de stabilité
Collaboration en équipe
Gestion de documents

Formazione

Diplôme en Sciences Pharmaceutiques, Chimie, Pharmacie ou Sciences Apparentées

Strumenti

Logiciels de laboratoire informatisés

Descrizione del lavoro

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FAMAR is a European contract manufacturing and development partner for the pharmaceutical and health & beauty industry. Building on our 70 years’ expertise, we deliver flexible solutions, from development to production and distribution. Driven by our customer-care mindset, we offer services covering the majority of pharmaceutical forms. Through the outstanding knowledge and commitment of our 1850 employees and with a network of 6 production sites, we supply a wide range of 1800 products in 125 international markets.

For the Italian plant in Baranzate specialising in the production of oral solids, we are currently looking for a Quality Control Scientist to join the Quality Control Laboratory.

In this role, you will play a crucial role in carrying out the analytical activities in full compliance with the company's times, procedures and standards of production efficiency and quality.

Skills & Responsibilities :

  • High proficiency in analytical instrumentation for the analysis of small and large molecules, particularly with the use of HPLC, GC, IR, UV-Spectrophotometer
  • Extensive experience in a cGMP environment in reviewing analytical documentation and knowledge of related issues concerning DI
  • Good understanding of regulatory practices and standards
  • Responsible for testing raw materials, in-process products, and finished products according to Standard Operating Procedures (SOPs)
  • Optimization of analytical methods; Transfer and validation of methods.
  • Preparation of protocols and reports concerning transfer and analytical validation activities in accordance with Company and International standards
  • Ensure that all activities conducted comply with SOPs and cGMP regulatory standards
  • Stability testing on finished products and intermediates
  • Review of analytical data in accordance with procedures
  • Knowledge of company procedures and GMP
  • Familiarity with laboratory computerized programs and management software
  • Collaborate with cross-functional teams to achieve company goals
  • Maintain accurate and complete records of activities performed
  • Strictly follow protocols and procedures to ensure compliance with regulatory and company standards
  • Determine and implement improvements to optimize workflows and processes
  • Participate in calls with clients for updates on activities and project status
  • Collaborate in conducting Internal and External Audits
  • Education : Degree in Pharmaceutical Sciences, Chemistry, Pharmacy or Related Sciences
  • Professional Experience : Minimum experience of 5 years in Pharmaceutical Industry
  • Strong experience in analytical validation activities and methods
  • Excellent organizational and planning skills
  • Order and precision in the execution of activities
  • Respect, transparency and good communication skills
  • Ability to work in a team

Seniority level

Seniority level

Associate

Employment type

Employment type

Full-time

Job function

Job function

Quality Assurance

Pharmaceutical Manufacturing

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