Process Technician (Inspection and Packaging)

CSL Plasma; Liverpool City Region; On-site; GBP 25,000 - 35,000; Full time

Job summary

CSL Plasma is seeking a skilled Process Technician for the Seqirus Liverpool site. The role involves overseeing inspection and packaging processes for vaccine production, ensuring compliance with cGMP and safety standards, while leading a team. Ideal candidates will have relevant experience in the biotech sector, proficiency with SAP and GLIMS, and a strong commitment to high-quality standards.

Benefits

Competitive salary

Career development opportunities

Health and wellness benefits

Employee assistance program

Qualifications

• Experience in inspection or packaging of aseptic products preferred.
• Knowledge of cGMP, FDA requirements is a plus.
• A basic mechanical aptitude or knowledge of equipment.

Responsibilities

• Responsible for inspection and packing in vaccine manufacturing.
• Ensure compliance with documentation and safety standards.
• Support team and resolve manufacturing issues.

Skills

cGMP knowledge

Interpersonal skills

Problem-solving

Lean manufacturing principles

Education

Relevant Degree

Tools

SAP

GLIMS

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 mandatory policies, guidelines, and site procedures.

When manufacturing, ensures that all departmental SOPs and MIs 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.
• Carry out final documentation review and sign off to ensure documentation is right 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, demonstrating behaviors necessary to create a safe working environment.

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 maintains and promotes a cGMP compliant culture, ensures the highest standards of housekeeping and safety, and applies lean manufacturing principles, problem solving, 5S, waste elimination, and energy-efficient activities in support of continuous improvement. Executes manufacturing-led 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.

This role works with the Team Leader to resolve issues encountered during manufacturing by providing improvement recommendations and working with stakeholders to implement corrective actions. The role involves maximizing individual contribution to achieve team objectives, supporting other departments when needed, and ensuring documentation is completed timely and compliantly. Extracts and interprets batch and system performance data (e.g., SAP & GLIMS) for problem solving and root cause analysis. Attends all required training and develops new skills to meet current and future business needs. Demonstrates application of role-specific skills.

Knowledge, Skills & Competencies

• Previous experience in inspection or packaging of aseptic products within a cold chain preferred.
• Good personal qualities and interpersonal skills, including concern for standards, integrity, communication, and discretion.
• Proficient in computer systems such as SAP & GLIMS.
• Knowledge of cGMP (and FDA requirements is a plus).
• Basic mechanical aptitude or knowledge of electronic/mechanical equipment.
• Proficiency in the local language.

Experience Requirements

Relevant experience and competence in cGMP and sterile product Inspection & Packaging operations in the biotech or pharma industry preferred, ideally within Inspection and Packaging. Experience with Groninger, Brevetti, or Marchesini machines is advantageous. A relevant Degree Qualification is preferred.

Our 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 the benefits available to employees.

About CSL Seqirus

CSL Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers worldwide, CSL Seqirus contributes significantly to influenza prevention and pandemic preparedness. Learn more about CSL Seqirus.

We want Seqirus to reflect the world around us

At CSL, Inclusion and Belonging are at our core. We celebrate differences and foster a culture of curiosity and empathy to better connect with our patients, donors, stakeholders, and workforce. Learn more about Inclusion and Belonging at CSL.

Do work that matters at CSL Seqirus!

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