Location:
Visp
Workload:
100%
Start Date:
Contract Duration:
12 months (until
Language Requirement:
Fluent English (German is an advantage)
Join our client's dynamic production team and contribute to the manufacturing of high-quality biopharmaceutical products. This is an excellent opportunity for experienced professionals to work in a cutting-edge environment while ensuring compliance with safety and cGMP standards.
Key Responsibilities
Perform assignments across various production functions in compliance with safety regulations and cGMP requirements.
Identify, interpret, and resolve deviations in production processes.
Execute production steps, including accurate documentation and calculations.
Support onboarding and training of new team members.
Your Profile
Completed education in chemical or biopharmaceutical fields.
Professional experience in pharmaceutical production (e.g., operator, production technician).
Strong safety awareness and adherence to SOPs.
Knowledge of process engineering.
Fluent in English; German language skills are a plus.
Interested?
Apply now with your CV.
Please note: Only candidates with the right to work in Switzerland can be considered ( EU citizens or holders of a valid Swiss work permit)