Process Technician - Seed

Adecco; Liverpool; On-site; GBP 25,000 - 35,000; Full time

Job summary

A recruitment agency is seeking a Skilled Pharmaceutical Operative for an aseptic processing role in Liverpool. The successful candidate will operate within a manufacturing environment, supporting the production of viral seed stocks for the Influenza Vaccine. Responsibilities include ensuring compliance with all SOPs, maintaining cleanliness in the workspace, and contributing to health and safety standards. Candidates with experience in a clean room and knowledge of GMP in aseptic areas are preferred. The role is contracted for 6 months and aims to uphold continuous improvement.

Qualifications

• Experience in an aseptic environment is essential.
• Skilled worker status is required.
• Practical knowledge of clean room operations.

Responsibilities

• Ensure all departmental SOPs and MLs are followed.
• Maintain a cGMP compliant culture and high safety standards.
• Contribute to process improvements and team objectives.

Skills

Experience in pharmaceutical, biotechnology sterile production

Knowledge of GMP in an aseptic area

Basic mechanical aptitude or knowledge of electronic mechanical equipment

Ability to work in clean room environment

Education

Technical training in a biotech program

Job description

Skilled Pharmaceutical Operative for Aseptic Processing Role in Speke Liverpool - 6 Month Contract - Aseptic Experience Essential

The role holder will be a key employee in the manufacturing organization. They 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. To be considered for this role you must have experience in an aseptic environment.

Responsibilities

• When manufacturing ensure that all Departmental SOPs and Ml's are followed and:
  Ensure appropriate control, monitoring and delivery of activities in their area of work.
  Ensure that all documentation is completed correctly, accurately in a timely manner and signed by the relevant personnel.
  Carryout final documentation review and sign off to ensure documentation is right first time.
  Ensure compliance to Health and Safety regulations. Consistently demonstrating the behaviours necessary to create a safe working environment for themselves and their colleagues
  Be able to update existing SOPs and Ml's as and when required performing regular reviews and initiating new documentation as appropriate.
• To actively maintain and promote a cGMP compliant culture, ensure that the highest standards of housekeeping and safety are applied within the area in accordance with the Orange Guide and CFR regulations and to apply the principles of Lean Manufacturing, Problem Solving, 5S ,Waste Elimination and Energy Efficient Activities in support of Continuous Improvement.
• To maximise their individual contribution so that team objectives are achieved.
  To work as a team member, providing and receiving support feedback to and from team members and their team leader.
  To communicate and liaise with members of other teams, customers and suppliers in order to meet the business's objectives.
  To suggest solutions to issues which may arise.
• Attend all compulsory and allocated training courses required for the role.
  Ensure that all training is completed in a timely manner and that personal training records are kept up to date.
  To continue to develop new skills, competencies and behaviours to fulfil both current and future business needs.
  The role holder will be able to demonstrate the application of the skills required for their role.
• To work in a safe manner in compliance with all pertinent UK legislation, mandatory policies, guidelines and site procedures for Health, Safety and Environment.
• To contribute ideas and action in order to improve team, process and equipment performance.
  To support process improvement and uphold Values and Behaviours.
• Support organisation change and process improvements.

Skills & Experience

• Skilled worker with relevant experience in pharmaceutical, biotechnology sterile production. Preference given to candidates with technical training in a bio tech program.
• Knowledge of GMP - In an ASEPTIC area.
• Basic mechanical aptitude or knowledge of electronic mechanical equipment.
• Ability to work in, training for, or practical knowledge of clean room environment operations.

Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.