Work with us

Quality Control Analyst

Olon S.p.A. is an Italian company, a world leader in the production of active ingredients (APIs) for the general market and in CDMO (Contract Development and Manufacturing).

Olon has 11 production sites: 8 in Italy, 1 in Spain, 1 in the USA and 1 in India and 3 commercial subsidiaries.

We are looking for Quality Control Analyst profiles to be placed in our plants in Rodano (MI), Mulazzano (LO) and Garbagnate Milanese (MI).

The resources, placed within the Quality Unit, will report to the Quality Control Laboratory Manager.

Specifically, they will be responsible for:

  • Perform analyses, define procedures and validations related to QC.
  • Perform analytical tests on chemicals and raw materials.
  • Accurately document the work process and test results in accordance with GMP requirements.
  • Write and review analytical procedures, SOPs, protocols and reports
  • Request materials and equipment needed for work activities and train staff to maintain them
  • Using HPLC in accordance with GMP and internal guidelines
  • Plan work to ensure correct project steps.
  • File and maintain appropriate documentation for the laboratory
  • Maintain up-to-date safety and environmental regulations in the laboratory
  • Write and review protocols, procedures and reports

The ideal candidate possesses:

  • Diploma and/or degree in chemical field
  • Knowledge of and compliance with regulations related to Environment, Health and Safety (HSE).
  • Basic knowledge of GMP / GDP rules, rules related to Environment Health and Safety (HSE) and proper use of Personal Protective Equipment (PPE)
  • Ability to work in full compliance with Data Integrity in order to ensure that data is attributable, understandable, up-to-date, original and accurate (ALCOA)
  • Ability to implement the rules of good behavior while maintaining the cleanliness of one’s workplace
  • Prior experience in Laboratory environment, knowledge of basic laboratory SOPs, quality Knowledge of analytical techniques, knowledge of GC Chromatographic instruments, HPLC, UHPLC is a requirement
  • Good knowledge of Office package
  • Willingness to work on deadlines with good energy level, self-motivation and high organizational skills
  • Willingness to work in shifts is required