ARD Analyst (Temporary)

Description

Job Summary: We are seeking an R&D Laboratory Analyst to maintain equipment, follow analytical methods, and collaborate on project development, with a focus on quality and organization. Key Responsibilities: 1. Maintain testing equipment and materials in good condition. 2. Follow analytical methods and support project development. 3. Perform measurements, calculations, calibration, and interpretation of GMP results. Reporting to the Analytical Development Laboratory Coordinator, this person will be assigned the following responsibilities: * Maintain in good condition the equipment and materials used in conducting tests * Follow established work instructions and analytical methods, supporting and collaborating on project development within required timeframes and quality standards * Record and document observed incident data * Perform measurement, calculation, calibration, maintenance, and interpretation activities for results obtained in the laboratory’s GMP activity area * Draft, in accordance with the quality system, the laboratory’s SOPs **WE OFFER**: * The opportunity to join a dynamic work environment based on trust and transparency. * Substitute contract (estimated duration of 3 to 9 months) * Attractive salary package and social benefits package **VACANCY 1**: * **Start date: Immediate** * Schedule: fixed afternoon shift (Monday to Friday: 14:00–22:00) **VACANCY 2**: * **Start date: June** * Flexible schedule (Monday to Friday: arrival between 07:00–10:00; Monday to Thursday: departure between 16:00–19:00; Friday: departure from 15:00 onwards) * Vocational Training Level II / Higher Vocational Training Certificate in Chemistry, Analysis and Control * Technical English * Minimum 2 years’ experience as an R&D laboratory analyst in the pharmaceutical industry (or similar). * Experience with chromatographic techniques (GC, HPLC, UPLC), spectroscopic techniques (UV, IR), and dissolution testing (USP I, II, III). Experience in development and validation of analytical methods for APIs, excipients, and finished products (tablets and capsules). * We seek individuals oriented toward quality, highly organized and planning-capable, methodical, systematic, and people-oriented.