Process Technician (Seed)

CSL; Liverpool; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading company in the biotechnology sector seeks a key employee for its manufacturing operation in Liverpool. The role involves supporting the production of viral seed stocks for Influenza Vaccine, ensuring compliance with regulations, and contributing to continuous improvement initiatives. Ideal candidates will possess experience in cleanroom environments and aseptic manipulations, along with a commitment to promoting a cGMP culture.

Qualifications

• Experience in A/B Grade cleanroom environments.
• Knowledge of cGMP regulations.
• Experience with controlled environments.

Responsibilities

• Follow SOPs and MLs during manufacturing activities.
• Complete documentation accurately and promptly.
• Maintain compliance with Health and Safety regulations.

Skills

Aseptic manipulations

Pharmaceutical sterile production

Mechanical aptitude

Job description

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You will be a key employee in the manufacturing organization, supporting the production of viral seed stocks for Influenza Vaccine manufacturing at our Liverpool site. Your responsibilities include:

1. Following all SOPs and MLs during manufacturing activities.
2. Controlling, monitoring, and ensuring the delivery of activities in your area.
3. Completing documentation accurately and promptly, with proper sign-offs.
4. Carrying out final documentation review to ensure correctness on the first attempt.
5. Maintaining compliance with Health and Safety regulations, fostering a safe working environment.
6. Updating existing SOPs and MLs as needed, performing reviews, and initiating new documentation.
7. Promoting a cGMP-compliant culture, maintaining high standards of housekeeping and safety, and applying principles of Lean Manufacturing, Problem Solving, 5S, Waste Elimination, and Energy Efficiency for Continuous Improvement.
8. Maximizing individual contributions to meet team objectives, supporting and communicating effectively with team members, and liaising with other teams, customers, and suppliers.
9. Attending all required training courses, maintaining training records, and developing new skills to meet current and future business needs.
10. Working safely in accordance with UK legislation, Seqirus policies, and site procedures for Health, Safety, and Environment.
11. Contributing ideas for process and team improvements, supporting process enhancements, and upholding Seqirus Values and Behaviors.
12. Supporting organizational change and process improvements.

Experience Requirements:

• Experience working in A/B Grade cleanroom environments.
• Experience with aseptic manipulations and working in controlled environments.
• Skilled in pharmaceutical or biotechnology sterile production.
• Knowledge of cGMP regulations.
• Mechanical aptitude and familiarity with electronic mechanical equipment.

Note: Qualifications or responsibilities may vary based on local legal and educational requirements. Please refer to local job documentation where applicable.

Seqirus is committed to attracting and retaining top talent who contribute to achieving our business objectives.