Project Support Associate, Client Services Distribution — Thermo Fisher Scientific (Schweiz) AG
CHF 62'000 - 94'000
Thermo Fisher Scientific (Schweiz) AG · Allschwil, Switzerland (BL)
- Ort
- Allschwil
- Vertrag
- full-time
- Veröffentlicht
- vor 15 Tagen
LohnCHF 62'000 - 94'000
Rollenüberblick
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale.
Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer.
- Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description
- As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale.
Unternehmen und Kontext
- Detail-oriented with excellent organizational and documentation abilities
- Demonstrated ability to work independently and as part of cross-functional teams
- Fluent English required, additional languages beneficial
- Experience coordinating with teams and managing stakeholder relationships
- Ability to analyze data and generate clear, accurate reports
- Focus on quality service and continuous improvement
- Adaptable to changing priorities while maintaining attention to detail
- Travel to client sites or other facilities may be required
Weitere Details
- Environmental Conditions
- We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
- You'll handle project planning, documentation management, and cross-functional coordination to meet timelines and client expectations.
Notizen und Originalinhalt
- Work Schedule
- Standard (Mon-Fri)
- Job Description
- DESCRIPTION:
- REQUIREMENTS:
- Bachelor's degree required, no prior experience required, preferably in clinical trials or pharmaceutical industry