Process Technician (Inspection and Packaging)

CSL (EMEA); United Kingdom; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading biotechnology firm in the United Kingdom is seeking a Process Technician to support the manufacturing processes of inspection and packing. This role requires a strong understanding of cGMP principles, as well as experience in aseptic product packaging. You will be responsible for maintaining the highest standards of safety and productivity. The ideal candidate should have relevant industry experience and be skilled in using SAP and GLIMS. Competitive benefits are offered.

Benefits

Comprehensive benefits package

Qualifications

• Experience in cGMP and sterile product inspection & packaging operations in biotech or pharma industry preferred.
• Experience with Groninger, Brevetti or Marchesini machines advantageous.
• Good personal qualities such as concern for standards, integrity, communication, and discretion.

Responsibilities

• Ensure control, monitoring, and delivery of activities.
• Develop and coach team members.
• Report incidents and ensure compliance with safety regulations.

Skills

Previous experience in inspection or packaging of aseptic products

Interpersonal skills

Competent in using computer systems (SAP, GLIMS)

Knowledge of cGMP

Basic mechanical aptitude

Education

Relevant degree qualification

Job description

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. Therefore, 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 that 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 to success.
• Continuous improvement and use of appropriate lean tools.
• Ensure compliance with health and safety regulations, consistently demonstrating the behaviours necessary to create a safe working environment for themselves and their colleagues.

Maintains the production team’s and site standards in EHS, cGMP, productivity, and costs. This includes reporting and escalation of incidents in a timely manner. Actively promotes a cGMP‑compliant culture, ensuring the highest standards of housekeeping and safety are applied within the area in accordance with regulations, applying lean manufacturing principles, 5S, waste elimination and energy‑efficient activities to support continuous improvement. Executes manufacturing‑lead tasks during equipment qualification and process validation in compliance with all safety and quality (cGMP) requirements. Participates in investigations (safety, quality, or other incidents) related to the I&P operation and works with stakeholders to identify and correct the root cause, implementing preventive actions to reduce recurrence.

This role works with the Team Leader to resolve issues encountered while executing manufacturing tasks by providing improvement recommendations, and collaborates with other stakeholders and process operators to implement corrective actions. Supports other departments flexibly when required, ensuring adequate training is received and the work is safe. Suggests solutions to arising issues, ensures documentation is completed compliantly and timely, extracts and interprets batch and system performance data (e.g., SAP & GLIMS) to enable timely problem solving and root‑cause analysis, attends all compulsory and allocated training courses, and keeps personal training records up to date. Continues to develop new skills, competencies, and behaviours to fulfil current and future business needs.

Knowledge, & Competencies

• 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.
• Competent 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.

Benefits

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 benefits you can participate in when you join CSL Seqirus.