Analista del controllo qualità senior

FAMAR; Pavia; In loco; EUR 40.000 - 55.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company in Pavia is seeking a Quality Control Scientist to join their Quality Control Laboratory. The role involves conducting analytical activities in compliance with cGMP standards and testing raw materials and finished products. Candidates should hold a degree in Chemistry or Pharmacy and have at least 3 years of experience in the pharmaceutical industry.

Competenze

• Minimum 3 years of professional experience in the pharmaceutical industry.
• Precision and orderliness in task execution.
• Ability to work effectively in a team.

Mansioni

• Carrying out analytical activities in compliance with company standards.
• Testing raw materials and finished products according to SOPs.
• Conducting stability testing on finished products.

Conoscenze

Proficiency in analytical instrumentation

cGMP environment experience

Knowledge of regulatory practices

Familiarity with laboratory software

Excellent organizational skills

Good communication skills

Formazione

Degree in Chemistry, Pharmacy, or related sciences

Strumenti

HPLC

GC

IR Spectrophotometry

UV Spectrophotometry

Descrizione del lavoro

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 analytical activities in full compliance with the company's standards, procedures, and efficiency goals.

Skills & Responsibilities :

• Proficiency in analytical instrumentation for the analysis of small and large molecules, especially HPLC, GC, IR, UV Spectrophotometry
• Experience in a cGMP environment, reviewing analytical documentation, and understanding related DI issues
• Knowledge of regulatory practices and standards
• Testing raw materials, in-process, and finished products according to SOPs
• Optimizing analytical methods; transferring and validating methods
• Preparing protocols and reports for transfer and validation activities in accordance with company and international standards
• Ensuring all activities comply with SOPs and cGMP standards
• Conducting stability testing on finished products and intermediates
• Reviewing analytical data following procedures
• Familiarity with laboratory software and management systems
• Collaborating with cross-functional teams to meet company objectives
• Maintaining accurate records of all activities
• Following protocols strictly to ensure regulatory and company compliance
• Implementing improvements to optimize workflows and processes
• Participating in client calls for updates on activities and projects
• Assisting in internal and external audits

Background & Soft Skills :

• Degree in Chemistry, Pharmacy, or related sciences
• Minimum 3 years of professional experience in the pharmaceutical industry
• Excellent organizational and planning skills
• Precision and orderliness in task execution
• Respectfulness, transparency, and good communication skills
• Ability to work effectively in a team