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Quality Control Scientist

FAMAR

Cascina Vignazza

In loco

EUR 30.000 - 45.000

Tempo pieno

2 giorni fa
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Descrizione del lavoro

A leading company in the pharmaceutical industry seeks a Quality Control Scientist for its plant in Baranzate. The candidate will carry out analytical activities, ensuring compliance with quality and production standards, and contribute significantly to maintaining the efficiency of processes. This role requires a degree in pharmaceutical sciences and a minimum of five years' experience in a cGMP environment.

Competenze

  • Minimum 5 years experience in the Pharmaceutical Industry.
  • Strong experience in analytical validation activities.
  • Excellent organizational and planning skills.

Mansioni

  • Conduct analytical activities in compliance with company standards.
  • Test raw materials and finished products according to SOPs.
  • Participate in internal and external audits.

Conoscenze

Analytical instrumentation proficiency
Knowledge of SOPs
Regulatory practices understanding
Collaboration skills
Good communication skills
Organizational skills

Formazione

Degree in Pharmaceutical Sciences, Chemistry, Pharmacy or Related Sciences

Strumenti

HPLC
GC
UV-Spectrophotometer

Descrizione del lavoro

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 DIG.
  • 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.

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Quality Control • Lombardia, Pavia, Italia

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