Website Achieva Group Limited
An excellent opportunity has arisen to join a leading pharmaceutical company as 2 Clinical Packaging Operator’s on initial 18 month contracts.
Perform assigned manufacturing tasks in hand packaging of clinical trial samples according to the production plan to enable timely production of the product in quality and quantity in accordance with relevant GMP, safety and environmental guidelines.
Tasks:
- Manual labeling and packaging of primary packaged drugs for clinical trials
- Carrying out all assigned activities in accordance with the production plan and the applicable GMP, work, operational, environmental and safety instructions and guidelines
- Timely and error-free preparation of batch documentation (part of production)
- Participation in the housekeeping of the production area (workplace cleaning, order, 5S, etc.)
- Compliance with health, safety and environmental rules and guidelines (HSE)
- Application of current GMP rules
- Carrying out process-related 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 weak points, propose improvement measures (organization, process, safety, hygiene, etc.) at the production site·
- Participation in all function-relevant training courses and maintaining the required level of training
- If necessary and if applicable, Willingness to work overtime or shifts (early and late shifts).
- Proposing improvement measures (organization, process, safety, hygiene, etc.) at the production facility
- Management/participation in continuous improvement projects in line with strategic objectives
- Collaboration with other units and willingness to work in other areas if required.
Requirements:
- Team player with good team spirit
- Adaptability, ability to work under pressure
- High sense of duty and care (documentation, order and cleanliness in the workplace)
- Constructive way of working, flexibility, solution-oriented, responsibility for one’s own work, deep understanding of quality
- Self-motivation and ability to learn
- Fine motor skills, enjoy working precisely
- Good knowledge of PC, MS Office. Knowledge of SAP is an advantage
- Good knowledge of MS Office and process control systems
- Knowledge/experience in the GMP environment and/or hypercritical areas is an advantage
- Good German