QA Professional

Olon S.p.A.; Milano; Hybrid; EUR 32,000 - 44,000; Full time

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 a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO and generic markets, integrating chemical synthesis and biological processes while always embracing the highest international safety, quality, and environmental standards.

Olon has a global network of 14 manufacturing sites and 9 RCD centers across the globe.

We are looking for a Quality Assurance Professional to be placed at the plant in Rodano (MI).

The resource will be placed within the Quality Unit and will report to the Quality Assurance Manager.

Specifically, the resource will be responsible for the following activities:

• 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

Requirements

• Master’s degree in Pharmaceutical Chemistry and Technology, Chemistry, 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

You will find:

• A dynamic, constantly evolving work environment, open to creativity and personal contribution
• Training Program to increase your personal and professional skills
• Courses for recent high school graduates and graduates
• Internal career paths: we believe in internal growth and cultivate our managers
• An inclusive environment that fosters integration of different cultures and mindsets

Olon is committed to providing equal opportunities in employment. Our policy foresees that equal employment opportunities are provided without regard to age, race, creed, color, religion, sex,

disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status and/or any legally recognized status entitled to protection under applicable local laws.