MASS SPECTROMETRY SCIENTIST

Kymos Group; Ancona; In loco; EUR 40.000 - 55.000; Tempo pieno

Descrizione del lavoro

A leading Contract Research Organization is seeking a Mass Spectrometry Scientist to design and supervise quality control testing. The ideal candidate has a Bachelor’s degree in Chemical Sciences and experience in GMP environments. Responsibilities include managing projects, writing technical documents, and supervising staff. This is a full-time, on-site role in Ancona, Italy.

Competenze

• Experience in managing technical documents associated with studies.
• Experience working in GMP environments.
• Experience in similar roles in the pharmaceutical industry.

Mansioni

• Design, supervise, and execute quality control testing.
• Manage assigned projects and keep deadlines.
• Write technical documents associated with studies.
• Direct and supervise experimental work of technical staff.
• Perform work in compliance with Good Manufacturing Practices.

Conoscenze

Knowledge of HPLC

Knowledge of GC techniques

Teamwork skills

Detail-oriented

Method development expertise

Formazione

Bachelor’s degree in Chemical or Biochemical Sciences

Descrizione del lavoro

Job Overview

Kymos Group is a growing Contract Research Organization part of the Kymos Group, committed to quality and innovation. Pharmaprogress offers GMP/GLP-certified services for a wide range of molecules, generics, biosimilars, antibodies, biomarkers, ADA, ADC, hormones, enzymes, and nucleic acids.

Position

Mass Spectrometry Scientist – Temporary, Full time, On site – Location: Ancona, Italy.

Responsibilities

• Design, supervise, and execute quality control testing of raw materials and finished products.
• Manage assigned projects, keep deadlines, and establish 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 work in compliance with Good Manufacturing Practices (GMP).

Requirements

• Bachelor’s degree in Chemical or Biochemical Sciences (Laurea in Scienze Chimiche o Biochimiche).
• Knowledge of HPLC and GC techniques with 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, OOS, CAPA).
• Experience working in GMP environments is required.
• Experience in similar roles in the pharmaceutical industry.
• Teamwork skills; detail‑oriented and able to achieve objectives.

Diversity & Inclusion

Kymos considers diversity and inclusion as key development priorities, offering equal opportunities for all people regardless of gender, nationality, sexual orientation, gender identity, age, religion, or any other personal characteristic.