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Technical Specialist QATSC

Technical Specialist QATSC

ViatrisVega Baja, Puerto Rico, USA
Hace más de 30 días
Tipo de contrato
  • A tiempo completo
Descripción del trabajo

Viatris Pharmaceuticals LLC

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 :

Providing high quality trusted medicines regardless of geography or circumstance;

Advancing sustainable operations and innovative solutions to improve patient health; and

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 Specialist, QATSC role will make an impact :

Key responsibilities for this role include :

Meet budget targets.

Responsible of Laboratory requisitions and inventory processes.

Identifies and implements cost improvements and avoidance (CIP) measures,

Participates in the preparation, analysis, and control of assigned portion(s) of annual budget of his or her area.

Identifies and implements new technology, systems, and equipment for QC Laboratories.

Provides technical support and training on new testing, systems, and techniques.

Responsible for the coordination of activities required on the Laboratories.

Equipment’s Calibration, PM and non – routine services

Equipment’s Validation

Method Validation and / or methods improvements

Raman & NIR

Support Method Validation and / or methods improvements activities.

Identifies and implements process improvement opportunities.

Identifies, configures, validates, and implements LIMS objects and / or structures (stability module, Standards and Reagents, Test Methods, Specifications, Instruments)

Support the coordination of activities required from QC in the transfer of new products and or existing products.

Development of Protocols, reports and specifications.

Review / approval of regulatory documentation

Acts as a liaison between technical development, QC and QA during the transfer of new products.

The minimum qualifications for this role are :

Education

Bachelor’s degree in pharmacy, chemistry, natural science, engineering, or other closely related area.

Chemist License is desired.

Experience

At least five (5) years of in the pharmaceutical industry with similar responsibilities.

Other requirements

Knowledgeable in Quality Systems.

Be able to proactively assess and influence RA from different countries related to site registrations including changes.

Proficient in computer software's such as Microsoft Office.

Ability to handle several priorities simultaneously.

Excellent negotiation skills, leadership, and analytical thinking

Fully bilingual both, verbal and written (English and Spanish)

Available to work and provide support during weekends and after working hours.

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. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.