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1 Vacancy
Job Description
Work Schedule
Rotational shift daysEnvironmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety StandardsJob Description
2-Shift Operation (Early Shift: 6 am - 2 pm; Late Shift: 2 pm - 10 pm) Job Description
Fisher Scientific Inc. with over 950 employees in Switzerland is a market leader in the areas of Clinical Supply Chain Management Services and clinical trial material manufacturing as well as global patient logistics. For more information about the site in Allschwil near Basel please visit our website:
Your Responsibilities:
Efficient and GMP-compliant execution of manufacturing control and packaging orders including in-process controls
Setting up/adjusting/operating/dismantling/cleaning of relevant machines and equipment
Cleaning of relevant rooms machines and equipment
Compliance with specific regulations during the packaging of clinical trial samples particularly GMP rules hygiene and safety regulations and the applicable Standard Operating Procedures (SOPs) and packaging instructions
Adherence to personal protective equipment (coveralls gloves mask goggles etc.)
Your Profile:
Experience in the pharmaceutical/food industry
Mechanical and pharmaceutical experience
Computer skills / basic knowledge of common MS Office applications
Good command of German both written and spoken is required
Solid basic mathematical knowledge
A sense of responsibility ability to work in a team and open communication
Every one of our 100000 extraordinary individuals at Thermo Fisher Scientific tells a unique story. Join us and contribute to our singular mission.
This job description is not intended to and does not encompass all duties and responsibilities that may be required or assigned in this addition to the tasks listed you may be asked by your team leader or manager to undertake further functionrelated responsibilities projects or duties as circumstances demand. These may include but are not limited to providing support in machine maintenance assisting with calibration or validation activities participating in process improvement or quality assurance initiatives helping with internal or external audits contributing to documentation and reporting of incidents or deviations delivering training or onboarding of new team members managing inventory or materials logistics or performing additional tasks outside your usual scope in order to meet operational demands. Your flexibility adaptability and willingness to assist in various capacities will be valuable in fulfilling the overall objectives of the team and organisation.
Employment Type
Full-Time
