MASS SPECTROMETRY SCIENTIST

Job Details

Location: Ancona (Italy) Contract: Temporary Working day: Full time Sector: Pharmaceutical and biopharmaceutical Vacancies: 1 Discipline: Technical Work modality: On site

Kymos Group – Pharmaprogress is a reliable Contract Research Organization part of the Kymos Group, a fast growing company with a strong commitment to quality and dedication to innovation. Our customers have access to a wide range of GMP/GLP‑certified and GCP‑compliant services and obtain a tailor‑made, personalised, genuinely flexible service into a unique selection of services for innovative small and large molecules, generics, biosimilars, antibodies, biomarkers, ADA (anti‑drug antibodies), ADC (antibody‑drug conjugates), hormones, enzymes and nucleic acids. Job Description We are looking for a Mass Spectrometry Scientist to ensure the correct development of assigned analytical projects. The Responsibilities Of The Position Include

Design, supervise, and execute quality control testing of raw materials and finished products. Manage assigned projects, keeping deadlines and establishing direct communication with clients. Write technical documents associated with studies (protocols, reports, standard procedures, certificates of analysis). Direct and supervise the experimental work of technical staff. Perform the work in compliance with Good Manufacturing Practices (GMP).

Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic. We are looking for a Scienziato in Spettrometria di Massa to ensure the correct development of assigned analytical projects. Le Responsabilità Della Posizione Includono

Progettare, supervisionare ed eseguire il controllo qualità delle materie prime e dei prodotti finiti. Gestire i progetti assegnati, rispettando le scadenze e stabilendo una comunicazione diretta con i clienti. Redigere documenti tecnici associati agli studi (protocolli, rapporti, procedure standard, certificati di analisi). Dirigere e supervisionare il lavoro sperimentale del personale tecnico. Eseguire il lavoro in conformità con le Norme di Buona Fabbricazione (GMP).

Requirements

Bachelor’s degree in chemical or Biochemical Sciences. Knowledge of HPLC and GC techniques, with an understanding of analytical development departments. Good knowledge of method development with liquid chromatography coupled to mass spectrometry techniques. Experience in managing technical documents associated with studies (standard procedures, certificates of analysis, deviations, OOSs, CAPAs, etc.). Experience working in GMP environments is required. Experience in similar roles in the pharmaceutical industry. Teamwork skills. Detail‑oriented and able to achieve objectives.

Requisiti

Laurea in Scienze Chimiche o Biochimiche. Conoscenza delle tecniche HPLC e GC, con comprensione dei dipartimenti di sviluppo analitico. Buona conoscenza dello sviluppo di metodi con tecniche di cromatografia liquida accoppiata alla spettrometria di massa. Esperienza nella gestione dei documenti tecnici associati agli studi (procedure standard, certificati di analisi, deviazioni, OOS, CAPA, ecc.). Esperienza di lavoro in ambienti GMP è richiesta. Esperienza in ruoli simili nell'industria farmaceutica. Capacità di lavorare in squadra. Orientamento ai dettagli e capacità di raggiungere obiettivi.

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