Pharma QA Specialist - Compliance & Validation

Olon S.p.A.

Milano

Hybrid

EUR 32,000 - 44,000

Full time

5 days ago
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Job summary

Olon Group is seeking a Quality Assurance Professional to be placed at the Rodano (MI) plant. You will report to the Quality Assurance Manager within the Quality Unit and support the QA function across documentation, data handling and batch release activities.

Key tasks include drafting QA documentation, verifying API compliance, managing changes and deviations, supporting investigations, and drafting validation protocols and reports, while collaborating with manufacturing and analytical teams.

Qualifications

  • Master’s degree in Pharmaceutical Chemistry and Technology, Chemistry, or Pharmacy.
  • Good knowledge of the English language.
  • Knowledge of computer tools.
  • Good knowledge of the office package.
  • Willingness to work in a team.
  • Accuracy and punctuality.
  • Good interpersonal skills.

Responsibilities

  • Drafting QA documentation and reporting.
  • Data collection and tabulation, as needed.
  • Supporting/editing procedures.
  • Verifying assigned APIs compliance to ensure proper release; Verifying production and analytical batch records.
  • Managing changes, investigations, deviations or OOS related to assigned APIs.
  • Support in any product complaints.
  • Drafting of validation protocols/reports.
  • Customer contacts for QA aspects.

Skills

English language
Office software
Computer tools
Team player
Accuracy and punctuality
Interpersonal skills

Education

Master’s degree in Pharmaceutical Chemistry and Technology, Chemistry, or Pharmacy

Job description

Olon Group is seeking a Quality Assurance Professional to be placed at the Rodano (MI) plant. You will report to the Quality Assurance Manager within the Quality Unit and support the QA function across documentation, data handling and batch release activities.

Key tasks include drafting QA documentation, verifying API compliance, managing changes and deviations, supporting investigations, and drafting validation protocols and reports, while collaborating with manufacturing and analytical teams.

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