Process Technician (Inspection and Packaging) 12 Month Fixed Term Contract

ZipRecruiter; Liverpool; On-site; GBP 25,000 - 32,000; Full time

Job summary

A leading company in the pharmaceutical industry seeks a Process Technician in Liverpool. In this role, you will oversee manufacturing processes, ensuring compliance with cGMP standards while promoting safety and efficiency. Ideal candidates will possess relevant degree qualifications and experience in aseptic production.

Benefits

Attractive benefits package

Commitment to diversity and belonging

Qualifications

• Experience in inspection or packaging of aseptic products preferred.
• Competent in computer systems like SAP and GLIMS.
• Good interpersonal skills and commitment to standards.

Responsibilities

• Execute manufacturing processes for inspection and packing.
• Ensure compliance with health and safety regulations.
• Develop and coach team members for continuous improvement.

Skills

Team collaboration

Problem solving

Lean manufacturing

Attention to detail

Education

Relevant degree qualification

Tools

SAP

GLIMS

Job description

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 behaviors to work to and 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 safely in compliance with all pertinent UK legislation, Seqirus policies, guidelines, and site procedures. Ensures that all departmental SOPs and MIs are followed, with appropriate control, monitoring, and delivery of activities in their area of work.

Ensures all documentation is completed correctly, accurately, timely, and signed by relevant personnel. Carries out final documentation review and sign-off to ensure accuracy. Develops and coaches team members and shifts to success. Promotes continuous improvement and the use of lean tools. Ensures compliance with health and safety regulations, demonstrating behaviors necessary to create a safe working environment.

Maintains production team and site standards in EHS, cGMP, productivity, and costs. Reports and escalates incidents promptly. Actively maintains and promotes a cGMP compliant culture, ensuring high standards of housekeeping and safety, and applying lean manufacturing principles, problem solving, 5S, waste elimination, and energy efficiency activities.

Executes manufacturing lead tasks during equipment qualification and process validation in accordance with site procedures and safety and quality (cGMP) requirements. Participates in investigations related to safety, quality, or other incidents, working with stakeholders to identify root causes and implement preventive actions.

Works with the Team Leader to resolve issues encountered during manufacturing tasks by providing improvement recommendations and collaborating with stakeholders and process operators to implement corrective actions.

Maximizes individual contribution to achieve team objectives. Communicates and liaises effectively with team members, other teams, customers, and suppliers. Supports other departments when required, provided training is received and it is safe to do so. Ensures documentation is completed compliantly and promptly.

Extracts and interprets batch and system performance data (e.g., SAP & GLIMS) for problem solving and root cause analysis. Attends all required training and maintains personal training records. Continually develops new skills, competencies, and behaviors to meet current and future business needs.

Demonstrates application of required skills for the role. Previous experience in inspection or packaging of aseptic products within a cold chain is preferred. Good personal qualities and interpersonal skills such as concern for standards, integrity, communication, and discretion are essential.

Competent in daily use of computer systems (e.g., SAP & GLIMS). Knowledge of cGMP (and FDA requirements is a plus). Basic mechanical aptitude or knowledge of electronic/mechanical equipment is advantageous. Relevant experience and competence in cGMP and sterile product inspection & packaging operations in biotech or pharma industries, ideally with experience on Groninger, Brevetti, or Marchesini machines.

Relevant degree qualification is preferred. This is a 12-month secondment opportunity. CSL Seqirus offers attractive benefits as part of its commitment to attracting and retaining top talent.

About CSL Seqirus: CSL Seqirus, part of CSL Limited, is a leading influenza vaccine provider globally and contributes significantly to pandemic preparedness. Learn more about CSL Seqirus.

We embrace diversity and belonging, reflecting the world around us. Join us to do work that matters. Watch our ‘On the Front Line’ video to learn more about CSL Seqirus.