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R&d analyst - analitical method dev. (temporary contract)

Como
Contratto a tempo determinato
Stage
Recordati
Pubblicato il 12 maggio
Descrizione

R&D Analyst - Analitical Method Dev. (Temporary contract)

ID: 2526

Date of Posting: Apr 27, 2026

Business Area: Research & Development

Job Type: Direct Employee

Territory:

Full-Time or Part-Time: Full Time

Seniority: Entry level

Job Purpose

We are looking for a position within the Analytical Development team, contributing to the development and life‐cycle support of high‐quality pharmaceutical products. The role offers direct involvement in analytical method development, validation and stability studies for products under development and selected marketed products. Designed for an early‐career professional, this role provides the opportunity to grow within a structured and collaborative development environment, working alongside experienced scientists and gaining exposure to cross‐functional activities with QC, QA, Manufacturing and Regulatory Affairs. The position is laboratory‐based at Recordati and requires eligibility to work in Italy.

Key Responsibilities

- Support analytical method development for Drug Products, APIs and excipients

- Perform routine laboratory analyses following approved methods

- Assist in method validation and transfer activities

- Accurately complete laboratory documentation

- Support stability studies (set up, sample pull, tracking and testing)

- Assist in troubleshooting analytical issues with senior team members

- Operate analytical instruments and laboratory software

- Support general laboratory activities and ensure compliance with SOPs and safety requirements

Required Education

- Bachelor's or Master's Degree in Chemistry, Pharmaceutical Chemistry, Pharmaceutical Sciences or related disciplines

- Academic internship or thesis in analytical/pharmaceutical laboratories preferred

Required Skills and Experience

- 6–12 months of laboratory experience (industry, internship or traineeship)

- Basic knowledge of analytical techniques

- Introductory understanding of GMP environment

- Team working attitude and willingness to learn

- Ability to work under supervision and follow procedures managing a large team.

- Basic knowledge of HPLC / UPLC and UV

- Understanding of analytical method development and validation principles

- Stability studies basics

- Use of laboratory software and data recording systems

Required Behaviours and Competencies

- Attention to detail and accuracy

- Reliability and compliance mindset

- Good organizational skills

- Collaborative and proactive attitude

- Openness to feedback and continuous learning

Required Languages

- Italian: fluent

- English: basic to intermediate

We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.

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