Technical Service Support - Internship

at  Viatris

Meda Pharma S.p.A.
At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
Viatris empowers people worldwide to live healthier at every stage of life.
We do so via:
Access – Providing high quality trusted medicines regardless of geography or circumstance;
Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership – Leveraging our collective expertise to connect people to products and services.
Every day, we rise to the challenge to make a difference and here’s how the Technical Service Support role will make an impact

Key responsibilities for this role include:

• Supports activities during industrial trials collecting final data of finished product for process verifications;
• Supports activities during cleaning in reference to the Cleaning protocol issued and approved by Technical Services manager and Quality Manager, collecting final data results due to close the final report;
• Conducts under Technical Services Officer oversee on lab and industrial trials for scale-up and industrial transposition. Manage stability protocol and report for lab trials;
• Conducts under Technical services Officer oversee on new packaging or new material feasibility collaborating with ETS & production functions and manage compatibility trials;
• Collaborates with the Quality Unit in the technical assessments of process Change Controls or raw material change supporting laboratory trials;
• Enter and manage till approval in Trackwise Incident/ Investigation or Action Item; can be ‘assigned to’ for CAPA or Trend Assessment or Effectivness Check;
• Collaborates with the team to Issue methods and manufacturing instructions according to GMP and mandatory requirements.

The minimum qualifications for this role are:

• Bachelor’s degree: Chemical & or scientific degree as Biologist or Pharmaceutical or experience in the chemical and laboratory field;
• Knowledge of scientific and legislative disciplines related to the use of substances for the development and preparation of cosmetics and food supplements. Notions of pharmaceutical technique;
• Good attitude to teamwork, dynamism and availability;
• A Knowledge of English: able to express him/herself spontaneously, very fluently and precisely, differentiating finer shades of meaning even in the most complex situations;
• Professional, often with limited relevant experience or working towards advanced education or license;
• Problems may require complex analytical or problem solving techniques to define and identify cause. Requires evaluation, interpretation and judgment to select the right course of action which may or may not be defined;
• Good communication skills, rapid and responsive in contingent operational activities; good command of the tasks assigned to them;
• Practical knowledge of quality management systems and good data collection and analysis skills. Aptitude for study and research, determination, methodology and applicative constancy.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.
Viatris is an Equal Opportunity Employer.

Key responsibilities for this role include:

• Supports activities during industrial trials collecting final data of finished product for process verifications;
• Supports activities during cleaning in reference to the Cleaning protocol issued and approved by Technical Services manager and Quality Manager, collecting final data results due to close the final report;
• Conducts under Technical Services Officer oversee on lab and industrial trials for scale-up and industrial transposition. Manage stability protocol and report for lab trials;
• Conducts under Technical services Officer oversee on new packaging or new material feasibility collaborating with ETS & production functions and manage compatibility trials;
• Collaborates with the Quality Unit in the technical assessments of process Change Controls or raw material change supporting laboratory trials;
• Enter and manage till approval in Trackwise Incident/ Investigation or Action Item; can be ‘assigned to’ for CAPA or Trend Assessment or Effectivness Check;
• Collaborates with the team to Issue methods and manufacturing instructions according to GMP and mandatory requirements

The minimum qualifications for this role are:

• Bachelor’s degree: Chemical & or scientific degree as Biologist or Pharmaceutical or experience in the chemical and laboratory field;
• Knowledge of scientific and legislative disciplines related to the use of substances for the development and preparation of cosmetics and food supplements. Notions of pharmaceutical technique;
• Good attitude to teamwork, dynamism and availability;
• A Knowledge of English: able to express him/herself spontaneously, very fluently and precisely, differentiating finer shades of meaning even in the most complex situations;
• Professional, often with limited relevant experience or working towards advanced education or license;
• Problems may require complex analytical or problem solving techniques to define and identify cause. Requires evaluation, interpretation and judgment to select the right course of action which may or may not be defined;
• Good communication skills, rapid and responsive in contingent operational activities; good command of the tasks assigned to them;
• Practical knowledge of quality management systems and good data collection and analysis skills. Aptitude for study and research, determination, methodology and applicative constancy