Analytical Development Specialist

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, while providing a particularly strong expertise in Liquids, Ointments and Creams. 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.

We are currently looking for a professional to fill the temporary position of Analytical Development Specialist (R&D), for four months (20 May 2024 - 20 September 2024).

Analytical Development Specialist (R&D) - TEMPORARY PLACEMENT

(ADS_4.2024)

The Analytical Development Specialist (R&D) will be responsible for performing complex and diverse tasks that directly support tech transfer projects and will be involved in analytical method development, optimization and validation according to currently effective guidelines to support regulatory submission.

Main Accountabilities / Responsibilities:

The Analytical Development Specialist will be responsible for the following:

• Analytical Method Validation and Verification studies of physicochemical methods (i.e HPLC, GC, Dissolution etc).
• of Analytical methods into quality control routine
• Statistical Analysis for raw data evaluation
• protocols and reports for Analytical method transfer/Validation and Verification
• various activities according to relevant guidelines
• Analytical Risk Assessment
• technical support to Analytical investigations during qualification
• working instructions for the implementation of the analytical methods in the Quality Control Laboratory
• Module 3 part and GAP identification

Candidate’s Profile:

• University Degree in Chemistry
• Master of Science Degree in Chemical Analysis-Quality Control will be considered an advantage
• 2-3 years of experience in Research and Development or Quality Control Department within the pharmaceutical sector
• Analytical thinking, attention to detail, communication skills and team work
• Ability to meet strict deadlines
• Good use of English language (both oral and written).
• Knowledge of the Greek, Spanish or Italian languages will be considered an advantage
• Ability to move between the Business Units of the company within the zone of Attica

Benefits

• Kilometer compensation or company bus transportation
• Personal and professional development
• Dynamic and multinational working environment