Process Technician (Formulation)
Seqirus UK - Liverpool
Job Type:
Full time
Posted on:
Offerta pubblicata 2 giorni fa
Job Requisition ID:
R-246954
Working under the Team Leader, the Process Technician is responsible for executing the manufacturing processes in the Formulation department in accordance with written procedures.
The role holder will provide (be trained in) the technical skill sets necessary to manufacture high quality vaccines in a compliant, efficient and cost-effective manner.
Responsibilities
Carry out all formulation process operations using local SOPs and batch documentation whilst in full compliance with cGMP to meet production schedule demands.
Work in a safe manner in compliance with all pertinent UK legislation, Seqirus mandatory policies, guidelines and site procedures for Health, Safety and Environment.
Ensure 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.
Ensure compliance to Health and Safety regulations.
Consistently demonstrate the behaviours necessary to create a safe working environment for themselves and their colleagues.
Actively maintain and promote a cGMP compliant culture, ensuring the highest standards of housekeeping and safety are applied within the area.
Apply the principles of Lean Manufacturing, Problem Solving, 5S, Waste Elimination, and Energy Efficient Activities in support of Continuous Improvement.
Maximise individual contributions to achieve team objectives.
Communicate and liaise with members of other teams to meet business objectives.
Attend all compulsory and allocated training courses required for the role.
Ensure that all training is completed in a timely manner and that personal training records are kept up to date.
Contribute ideas and actions to improve team, process and equipment performance.
Support organisational change and process improvements.
Formulation – Specific Tasks Include:
Carry out process operations such as formulation, buffers, MF59 bulk and MF59 sterile filtration using cGMP, MES, EBR as required.
Move materials required in F&B (pallet trucks, mobile vessels, rigs, raw mats, etc.) using cGMP, MES, EBR systems as required.
Carry out basic area cleaning as required to maintain EM, cGMP and HSE standards in the F&B area.
Perform in Process Control checks and Environmental Monitoring.
Complete documentation to the required standards of accuracy, timeliness, and cGMP compliance.
Experience Requirements
Relevant experience in pharmaceutical, biotechnology sterile production.
Experience of gowning or working to a minimum Grade C Cleanroom environment.
Experience of Aseptic processing e.g. sterile connections, filter testing preferable.
Experience of cleaning cycles for both mobile and fixed Vessels (CIP/SOP and SanIP/SOP).
Proven knowledge of cGMP. Computer competent (e.g., PCS, GLIMS, SAP, MES).
Our Benefits CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives.
About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL). 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.
We want Seqirus to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion.
Do work that matters at CSL Seqirus! Watch our ‘On the Front Line’ video to learn more about CSL Seqirus.
Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please click here.
#J-18808-Ljbffr
Job Type:
Full time
Posted on:
Offerta pubblicata 2 giorni fa
Job Requisition ID:
R-246954
Working under the Team Leader, the Process Technician is responsible for executing the manufacturing processes in the Formulation department in accordance with written procedures.
The role holder will provide (be trained in) the technical skill sets necessary to manufacture high quality vaccines in a compliant, efficient and cost-effective manner.
Responsibilities
Carry out all formulation process operations using local SOPs and batch documentation whilst in full compliance with cGMP to meet production schedule demands.
Work in a safe manner in compliance with all pertinent UK legislation, Seqirus mandatory policies, guidelines and site procedures for Health, Safety and Environment.
Ensure 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.
Ensure compliance to Health and Safety regulations.
Consistently demonstrate the behaviours necessary to create a safe working environment for themselves and their colleagues.
Actively maintain and promote a cGMP compliant culture, ensuring the highest standards of housekeeping and safety are applied within the area.
Apply the principles of Lean Manufacturing, Problem Solving, 5S, Waste Elimination, and Energy Efficient Activities in support of Continuous Improvement.
Maximise individual contributions to achieve team objectives.
Communicate and liaise with members of other teams to meet business objectives.
Attend all compulsory and allocated training courses required for the role.
Ensure that all training is completed in a timely manner and that personal training records are kept up to date.
Contribute ideas and actions to improve team, process and equipment performance.
Support organisational change and process improvements.
Formulation – Specific Tasks Include:
Carry out process operations such as formulation, buffers, MF59 bulk and MF59 sterile filtration using cGMP, MES, EBR as required.
Move materials required in F&B (pallet trucks, mobile vessels, rigs, raw mats, etc.) using cGMP, MES, EBR systems as required.
Carry out basic area cleaning as required to maintain EM, cGMP and HSE standards in the F&B area.
Perform in Process Control checks and Environmental Monitoring.
Complete documentation to the required standards of accuracy, timeliness, and cGMP compliance.
Experience Requirements
Relevant experience in pharmaceutical, biotechnology sterile production.
Experience of gowning or working to a minimum Grade C Cleanroom environment.
Experience of Aseptic processing e.g. sterile connections, filter testing preferable.
Experience of cleaning cycles for both mobile and fixed Vessels (CIP/SOP and SanIP/SOP).
Proven knowledge of cGMP. Computer competent (e.g., PCS, GLIMS, SAP, MES).
Our Benefits CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives.
About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL). 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.
We want Seqirus to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion.
Do work that matters at CSL Seqirus! Watch our ‘On the Front Line’ video to learn more about CSL Seqirus.
Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please click here.
#J-18808-Ljbffr
