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Clinical Packaging Operator – 6238

 

Our client is a leading global player in the Pharmaceutical industry with global headquarters in Basel, Switzerland. They are undergoing a transformation with respect to culture and outside perception. The organisation focusses on novel therapies in Oncology and Ophthalmology and is also currently developing a world-leading pipeline in Neuroscience and Dermatology with one of the strongest pipelines of Phase II/III studies in the world.

We are currently looking for a Clinical Packaging Operator for a 18 months contract to be Basel

 

Purpose:

Perform assigned manufacturing tasks in the hand packaging of clinical trial samples according to the production schedule to enable timely production of product in quality and quantity according to relevant GMP, safety and environmental guidelines

 

 

Main Responsibilities:

·        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

·        Good German & English

 

 

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