Process Technician (Aseptic Filling)

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

Job summary

A leading biotechnology company in Liverpool is looking for a Process Technician (Aseptic Filling) to ensure compliance with cGMP during sterile filling operations. Responsibilities include performing filling operations, conducting control checks, and maintaining documentation. Candidates should have experience with aseptic techniques and possess a relevant degree or pharmaceutical experience.

Qualifications

• Experience in sterile product filling, aseptic techniques, and isolator technology.
• Strong documentation skills and ability to operate material handling equipment.
• Experience in a cGMP sterile manufacturing environment.

Responsibilities

• Perform sterile filling operations following cGMP.
• Conduct in-process control checks and environmental monitoring.
• Complete documentation for work orders and incident reports.

Skills

Sterile product filling

Aseptic techniques

Knowledge of cGMP

Documentation skills

Operating material handling equipment

Education

Degree qualification

Relevant pharmaceutical experience

Tools

PCS

GLIMS

SAP

Job description

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Process Technician (Aseptic Filling), Liverpool

Client:

CSL

Location:

Liverpool, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

b7ad0334e404

Job Views:

7

Posted:

12.08.2025

Expiry Date:

26.09.2025

Job Description:

Reporting to the Team Leader, the Process Technician (Aseptic Filling) is responsible for providing the necessary production skills to complete sterile filling operations, ensuring safety, cGMP compliance, and cost-effectiveness to meet production schedules.

Responsibilities:

• Perform sterile filling operations following cGMP, Batch records, and SOPs, ensuring compliance with local SOPs and HSE procedures.
• Move materials (pallet trucks, tanks, rigs) in accordance with cGMP, BR systems, and safety procedures to meet production targets.
• Maintain environmental standards through cleaning and environmental monitoring.
• Conduct in-process control checks and environmental monitoring to ensure process control and product quality.
• Accurately complete documentation, including work orders and incident reports, and address PCS, GLIMS, SAP issues as they arise.

Experience Requirements:

• Experience in sterile product filling, aseptic techniques, and isolator technology, with high compliance standards.
• Knowledge of cGMP and proficiency with PCS, GLIMS, SAP systems.
• Strong documentation skills and ability to operate material handling equipment.
• Experience in a cGMP sterile manufacturing environment within biotech or pharma industries.

Education Requirements:

• Degree qualification preferred or relevant pharmaceutical experience.
• Additional qualifications or responsibilities may vary based on local legal and educational requirements.

CSL Seqirus is committed to attracting and retaining top talent to achieve business objectives.