Manual labeling and packaging of primary packaged drugs for clinical trials
Perform all assigned activities according to the production plan and applicable GMP, labor, operational, environmental and safety instructions and guidelines
Timely and accurate preparation of batch documentation (part of production)
Collaboration in the housekeeping of the production area (workplace cleaning, order, 5S, etc.)
Compliance with health, safety and environmental rules and guidelines (HSE)
Application of the current GMP rules
Implementation of in-process controls
Correct and accurate documentation of the activities carried out on paper and in the electronic batch documentation, in accordance with GMP regulations
Willingness to continuously improve and analyze weaknesses, propose improvement measures (organization, process, safety, hygiene, etc.) at the production site
Participate in all functional training and maintain a required level of training
If required and if applicable, willingness to work overtime or shift work (early and late shift).
Propose improvement measures (organization, process, safety, hygiene, etc.) at the production site
Manage / participate in continuous improvement projects according to strategic objectives
Collaboration with other units and willingness to work in other areas as required.
Qualifications and Experience :
Relevant working / residency permit or Swiss / EU-Citizenship required
Team player with good team spirit
Adaptability, ability to work under pressure
High sense of duty and diligence (documentation, order and cleanliness in the workplace)
Constructive way of working, flexibility, solution-oriented, responsibility for own work, deep understanding of quality
Self-motivation and ability to learn
Fine motor skills, enjoyment of precise work
Good knowledge of PC, MS Office. Knowledge of SAP an advantage
Good knowledge of MS Office and process control systems
Knowledge / experience in GMP environment and or hypercritical areas an advantage