Pds analytical development
Pubblicato il 03-09-2026 - Gi Group SpA Filiale di Frosinone in Frosinone
FILIALE: FROSINONESPECIALIZZAZIONE: CORE SKILL - Life Science
Possiede le competenze per ricoprire questo ruolo? Legga i dettagli completi qui sotto e invii la sua candidatura oggi stesso.
Grafton LifeScience* is a dedicated team focused on enhancing the experiences, skills, and potential of candidates in Sales & Marketing, Clinical Research, Regulatory, and Operations within the Pharmaceutical and Medical sectors. We also specialize in roles related to customer support in the health-impacting distribution field (Pharmacies and Parapharmacies).We are a team of passionate professionals working to guide our candidates towards roles and corporate environments that best match their skills and expectations.
In partnership with an integrated CDMO with around 60 locations worldwide, specializing in integrated sterile liquid and lyophilized product development and commercial manufacturing, we offer an opportunity for
PDS Analytical Development & GMP Technician
The main function of a PDS Analytical Development & GMP Technician is to perform chemical analyses and support laboratory operations within the QC PDS Laboratory. This role ensures compliance with GMP standards, SOPs, and safety regulations while contributing to documentation, equipment maintenance, and continuous improvement initiatives.
Job Responsibilities:
- Use and control analytical equipment in the laboratory.
- Execute chemical analysis of semi-finished products, finished products, stability samples, and products under transfer or validation studies.
- Monitor the progress of analyses according to priorities defined by the Team Leader and company quality standards.
- Contribute to the correct management and calibration of laboratory equipment in compliance with GMP and regulatory standards.
- Support laboratory investigations for out-of-specification (OOS) results or deviations
Do you have these skills and requirements?
MSc in a scientific/pharmaceutical area, knowledge of GMP regulations and pharmaceutical m