By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’sand .
I further attest that all information I submit in my employment application is true to the best of my knowledge.
About the role :
This is an exciting career opportunity for a dynamic, autonomous, continuous improvement minded and change agile professional to embrace a team-based culture and more specifically within the Quality Control teams within a world-class Biotech GMP manufacturing environment.
The job holder supports analytical instrument lifecycle management for new and existing laboratory systems of the QC laboratories of Neuchâtel - Switzerland.
He is also responsible for ensuring fitness for intended use of Analytical Instrument and compliance with applicable regulatory requirements.
This is a short term 15 months contract.
You will have though the chance to apply internally to other job opportunities!
How you will contribute :
Comply with cGMPs and DI requirements through applicable guidelines and procedures
Take part in lab systems initiatives and projects
Support lab. systems introduction, upgrades, or maintenance
Support and interface with process owners of lab. systems
Translate user requirements into technical specifications following global standards and practices
Review / Execute qualification and / or validation protocols as needed
Provide training, documentation, and post-qualification support to users
Maintain and schedule preventative / corrective maintenance and calibration
Maintain data integrity standards for all lab. systems and instruments
Provide technical assessments on change controls, deviations, and investigations
Support and prepare inspections, audit responses and regulatory submissions
What you bring to Takeda :
Education & Experience
Master’s Degree in a scientific field related to the lab. (, Chemistry, Microbiology or Biology)
Extensive experience with instrument lifecycle requirements for cGMPs laboratory systems
Demonstrated practical experience in lab. systems implementation projects
Fluent in French and English (C1 written and spoken)
Detailed understanding of DI requirements and standard regulations for cGMPs operations
Strong team member with demonstrated ability to work effectively on cross-functional teams
Ability to work independently in a fast-paced environment and manage multiple projects and priorities
Effective organization, communication, presentation and influencing skills
What Takeda can offer you :
Full accident cover
Participation in health insurance premiums
Advantageous retirement plans
Financial participation in the sports practices of its employees
Transportation : support in local public transport, free parking, carpooling program
Takeda Neuchâtel offers to its employees an attractive framework and working conditions. The well-being, safety, development and career development of its employees are at the heart of our vision and of our Human Resources, Health, Environment and Safety policies.
Takeda Neuchâtel is an employer committed to its employees and future generations.
More about us :
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do.
We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.