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You will be a key employee in the manufacturing organization. You will operate and perform a broad range of varied work activities which support the team objectives. The purpose of the role is to support the manufacture of viral seed stocks for use in the Influenza Vaccine manufacturing process. You will report to the Process Leader (Formulation). The role is based at our Liverpool site.
Responsibilities:
1. Ensure that all Departmental SOPs and MIs are followed.
2. Ensure appropriate control, monitoring, and delivery of activities in their area of work.
3. Complete all documentation correctly, accurately, and in a timely manner, signed by the relevant personnel.
4. Carry out final documentation review and sign off to ensure documentation is right the first time.
5. Ensure compliance with Health and Safety regulations, demonstrating behaviors necessary to create a safe working environment.
6. Update existing SOPs and MIs as required, performing regular reviews and initiating new documentation as appropriate.
7. Maintain and promote a cGMP compliant culture, ensuring high standards of housekeeping and safety, applying Lean Manufacturing principles.
8. Maximize individual contributions to achieve team objectives, working as a team member and communicating with other teams, customers, and suppliers.
9. Attend all compulsory and allocated training courses required for the role, ensuring timely completion and keeping personal training records up to date.
10. Work in a safe manner in compliance with all pertinent UK legislation, Seqirus mandatory policies, guidelines, and site procedures for Health, Safety, and Environment.
11. Contribute ideas and actions to improve team, process, and equipment performance while supporting process improvement.
12. Support organizational change and process improvements.
Experience Requirements:
1. Experience in working in A/B Grade clean room environment operations.
2. Experience of aseptic manipulations and working in a controlled environment.
3. Skilled worker with relevant experience in pharmaceutical, biotechnology sterile production.
4. Knowledge of cGMP.
5. Mechanical aptitude and knowledge of electronic mechanical equipment.
6. Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives.
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