Overview
Location: Ancona (Italy)
Contract: Temporary
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Discipline: Quality
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 a dedication to innovation. We offer GMP/GLP‑certified and GCP‑compliant services, spanning small and large molecules, generics, biosimilars, antibodies, biomarkers, ADA, ADC, hormones, enzymes, and nucleic acids.
Scientist – Quality Control
Responsibilities
The design, supervision, and execution of quality control studies.
Managing the assigned projects, keeping deadlines and maintaining direct contact with the client.
Technical document writing associated with the studies (protocols, reports, standard procedures, certificates of analysis, etc.).
Directing and supervising the experimental work of the technical staff in charge.
We offer a position in a growing company with international projection and a salary based on experience and knowledge.
Requirements
Degree/Laurea in Chemistry, Pharmacy or equivalent.
Minimum 2 years of experience in chemical analysis of active principles and pharmaceutical forms in Analytical Development and Quality Control departments in the pharmaceutical sector.
Proficiency in HPLC/UHPLC, CG, and basic analytical development techniques such as dissolution tests, potentiometry, Karl Fischer, atomic absorption, etc.
High level of English.
Kymos considers diversity and inclusion as key development priorities, with a main goal of promoting a culture that embraces differences and celebrates unique talents. We are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.
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