Open Positions - Scientist (Join Us!)

Kymos Group; Ancona; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A pharmaceutical company located in Ancona is seeking a Scientist – Quality Control. This role involves designing and executing quality control studies, managing projects, and writing technical documents. Candidates should have a degree in Chemistry or Pharmacy and at least 2 years of experience in the pharmaceutical sector. Proficiency in HPLC/UHPLC and a high level of English are required.

Competenze

• Minimum 2 years of experience in Analytical Development and Quality Control.
• Experience with chemical analysis of active principles and pharmaceutical forms.

Mansioni

• Design, supervision, and execution of quality control studies.
• Managing projects and maintaining client contact.
• Writing technical documents like protocols and reports.
• Supervise the experimental work of the technical staff.

Conoscenze

HPLC/UHPLC proficiency

Chemical analysis

Basic analytical development techniques

High level of English

Formazione

Degree/Laurea in Chemistry, Pharmacy or equivalent

Descrizione del lavoro

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.