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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 to support team objectives. The role's purpose is to support the manufacture of viral seed stocks for use in Influenza Vaccine production. You will report to the Process Leader (Formulation). The role is based at our Liverpool site.
Responsibilities
1. Follow all Departmental SOPs and MLs during manufacturing activities, ensuring appropriate control, monitoring, and delivery of tasks.
2. Complete all documentation accurately, timely, and obtain signatures from relevant personnel.
3. Conduct final documentation review and sign-off to ensure accuracy on the first attempt.
4. Maintain compliance with Health and Safety regulations, fostering a safe working environment.
5. Update existing SOPs and MLs as required, performing reviews and initiating new documentation when appropriate.
6. Promote a cGMP-compliant culture, uphold high standards of housekeeping and safety per the Orange Guide and CFR regulations, and apply Lean Manufacturing, Problem Solving, 5S, Waste Elimination, and Energy Efficiency principles for Continuous Improvement.
7. Maximize individual contributions to achieve team objectives, communicate effectively with team members, other teams, customers, and suppliers, and suggest solutions for arising issues.
8. Attend all mandatory training, complete it promptly, and maintain up-to-date personal training records. Develop new skills and competencies to meet current and future business needs.
9. Work safely in accordance with UK legislation, Seqirus policies, guidelines, and site procedures related to Health, Safety, and Environment.
10. Contribute ideas and actions to improve team, process, and equipment performance, supporting process improvements and upholding Seqirus Values and Behaviors.
11. Support organizational change and process improvements.
Experience Requirements
* Experience working in A/B Grade cleanroom environments.
* Experience with aseptic manipulations and working in controlled environments.
* Relevant experience in pharmaceutical or biotechnology sterile production.
* Knowledge of cGMP standards.
* Mechanical aptitude and knowledge of electronic mechanical equipment.
* Qualifications or responsibilities may vary based on local legal and educational requirements; refer to local job documentation.
Seqirus is committed to attracting and retaining top talent who contribute to achieving business objectives.
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