Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life! 

 Novartis partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit.

 Ready to work with/through Magnit at Novartis? Please read on…

Major Accountabilities:

• Performs, supports or supervises instrument related qualification activities and change control including issuing, review and LU approval of corresponding documentation. 
• Responsible for instrument life-cycle activities like calibration and re-qualification.
• Serves as the point of contact between local QA and local ARD and service provider (if applicable) for inquiries regarding instrument related processes and represents global ARD in related networks, committees, and initiatives, if necessary, and collaborates with Qualification Experts and similar roles within global TRD.
• Supports establishing and maintenance of a GMP management system for analytical instruments at ARD. Responsible for maintaining the instrument database in GMP management system for analytical instruments in ARD.
• Oversees the GMP instrument activities within local ARD and coordinates the annual update of the validation master plan when required. Serves as the first point of contact between local QA and local ARD for general inquiries.
• Represents global ARD in analytical instrument related initiatives as appropriate. Provides advice and assistance to staff on analytical instrument related problems and deviations.
• Supports employee and contractor training programs in coordination with other roles and ensures that sufficient and appropriate training is provided.
• Writes and reviews instrument-related qualification documents and guidelines. Writes, reviews or provides input during the update of instrument-related re-qualification and calibration documents and guidelines.
• Compares externally determined calibration results with the specific requirements for the instrument to be applied, if required by the instrument use SOP. Supports audits, inspections and laboratory walk-throughs in terms of preparation, conducting and following up.

Requirements:

• University Master's degree.
• 5 -6 years Analyst experience / QA experience / Instrument management experience / Instrument Qualification experience.
• Experienced in managing deviations related to analytical instruments in compliance with Novartis and regulatory standards. 
• Author of procedures for instrument and system management.
• Good communication skills, flexibility for a dynamic environment, eager to learn and grow in different area, accountability.

Workload: 80 - 100% possible
Role type: Onsite
Required start date: June 2025

Why Novartis: 
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?

EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

Accommodation: 
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.