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Validation - MSAT, Segrate

Created 12/15/2021
Reference 743999792818918
Category Pharmaceuticals
Job type Full Time
Country Italy
City Segrate
Zip Not specified
Salary Competitive
Company Description

At LEO Pharma, we are pioneering together.
We help people with skin diseases live fulfilling lives by advancing dermatology beyond the skin.
We drive dermatology with our knowledge, collaboration and curiosity. We are at the forefront of science in developing new medicines for dermatology.
Each one of us at LEO Pharma can make a real impact in our everyday work. Together, we explore new ideas and make them happen. We do this through mutual respect and a shared sense of purpose, rooted in our caring culture and a commitment to helping others.
For us, pioneering together is about constantly improving and extending what's possible for each other, our company, and our patients.


    Job Description

    Are you ready to start a new adventure pioneering together with us?

    As Validation (Specialist or Technician), you will support the activities of Segrate site as manufacturing process expert

    Your main responsibilities will be:

    • Evaluate changes to processes, materials (excipients, active ingredients and packaging materials) and equipment;
    • Support the investigation of deviations, complaints and corrective actions collaborating with the rest of the team and the other functions;
    • Review production documentation and regulatory document for registration
    • Support technology transfers;
    • Train people in terms of process development and about procedures related to the manufacturing process;
    • Guarantee that processes are validated and that the monitoring is performed in an effective way;
    • Support the planning of cleaning and process validation activities, as well as the drafting of validation protocols and reports;
    • Execute the production and the packaging of trial batches of semisolids in a lab scale;
    • Check in complete autonomy the main procedures and analytical methods;
    • Perform the main analytical techniques needed to execute physical analysis of semisolids (mainly macroscopic and microscopic appearance, consistency and viscosity test);
    • Fill in complete autonomy production and analytical documentation.

    Qualifications

    • Master degree in Chemistry, Chemistry and Pharmaceutical Technology or Pharmacy
    • Experience of 1/3 years in a pharmaceutical technology lab or in departments as Production, Quality or Development
    • Knowledge of the main analytical techniques and validation principles
    • Good knowledge of the Good Manufacturing Practices
    • Good knowledge of Italian and English (written and spoken)
    • Good knowledge of MS Office package;
    • Collaboration skills both at a local and a global level
    • Flexibility and problem solving
    • Curiosity and continuous learning oriented
    • Performance and process optimization oriented

    Additional Information

    Join our mission to help more people achieve healthy skin
    Hundreds of millions of people around the globe are suffering from an untreated skin disease. Helping these people to get a better life is what LEO Pharma is all about. By understanding their needs and wishes we will improve existing treatments and break new land to uncover the solutions of tomorrow.

    By joining LEO Pharma you will get the opportunity to create results, develop yourself among highly skilled colleagues while taking on our quest to become the preferred dermatology care partner improving people's lives around the world and at the same time create profitable growth.

    Please submit your application by 31 December 2021.
    Please note that we review applications and conduct interviews on an ongoing basi s.