Process Technician (Inspection and Packaging)

CSL Seqirus; Liverpool; On-site; GBP 30,000 - 40,000; Full time

Job summary

A pharmaceutical company in Liverpool seeks a Process Technician to oversee manufacturing processes for inspections and packing. The ideal candidate should have experience in aseptic product handling and knowledge of compliance standards. Responsibilities include documentation, training team members, and maintaining safety regulations. This role offers a chance to contribute significantly to vaccine production and public health.

Qualifications

• Experience in inspection or packaging of aseptic products preferred.
• Good communication and integrity.
• Competency in SAP and GLIMS.
• Knowledge of cGMP and FDA requirements a plus.

Responsibilities

• Control and monitor activities in the work area.
• Ensure accurate and timely documentation.
• Develop and coach team members.
• Ensure compliance with health and safety regulations.

Skills

Inspection skills

Packaging skills

Interpersonal skills

Basic mechanical knowledge

Computer systems proficiency

Education

Relevant degree qualification

Tools

SAP

GLIMS

Job description

Overview

Working under the Team Leader, the Process Technician is responsible for the manufacturing processes of inspection and packing (I&P) at Seqirus Liverpool by executing manufacturing operations in accordance with written procedures. This position is for an operator with the necessary skills and behaviours to achieve core 3 level. Subject‑matter expert and people‑leading experience/aptitudes are relevant in candidate criteria selection. The role holder will help provide the technical skill set necessary to manufacture high quality vaccines in a compliant, efficient, and cost‑effective manner. Works in a safe manner in compliance with all pertinent UK legislation, Seqirus mandatory policies, guidelines, and site procedures.

Responsibilities

• Ensure appropriate control, monitoring and delivery of activities in their area of work.
• Ensure all documentation is completed correctly, accurately in a timely manner and signed by the relevant personnel.
• Carry out final documentation review and sign off to ensure documentation is right the first time.
• Develop and coach team members and shift success.
• Continuous improvement and use of appropriate lean tools.
• Ensure compliance to health and safety regulations, maintaining a safe working environment.
• Maintain the production team’s and site standards in EHS, cGMP, productivity and costs; report and escale incidents timely.
• Execute manufacturing‑lead tasks during equipment qualification and process validation, following site procedures and cGMP requirements.
• Participate in investigations (safety, quality, or other incidents) related to the I&P operation, work with stakeholders to identify root cause and implement preventive actions.
• Work with the Team Leader to resolve issues, provide improvement recommendations, and implement corrective actions.
• Communicate and liaise with other teams, customers, suppliers to meet business objectives.
• Support other departments flexibly, ensuring adequate training and safety.
• Extract and interpret batch and system performance data (e.g., SAP & GLIMS) for timely problem solving and root cause analysis.
• Attend and complete all compulsory and allocated training courses in a timely manner; keep personal training records up to date.
• Continuously develop skills, competencies and behaviours to fulfil current and future business needs.

Qualifications

• Previous experience in inspection or packaging of aseptic products held within a cold chain (preferred).
• Good personal qualities and interpersonal skills such as concern for standards, integrity, communication and discretion.
• Competency in the daily use of computer systems, e.g., SAP & GLIMS.
• Demonstrated knowledge of cGMP (and FDA requirements a plus).
• Basic mechanical aptitude or knowledge of electronic/mechanical equipment.
• Local language proficiency.

Experience Requirements

• Relevant experience and competence in cGMP and sterile product Inspection & Packaging operations in Biotech or Pharma industry preferred, ideally within Inspection and Packaging.
• Experience with Groninger, Brevetti or Marchesini machines advantageous.
• Relevant degree qualification preferred.

About CSL Seqirus

CSL Seqirus is committed to attracting and retaining world‑class employees who are valued for their contributions to achieving business objectives. Learn more about some of the you can participate in when you join CSL Seqirus.

is part of . As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state‑of‑the‑art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.

We want Seqirus to reflect the world around us.

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more.

Do work that matters at CSL Seqirus!

Watch our 'On the Front Line' video to learn more about CSL Seqirus