Average Process Technician salary in Liverpool

Cpl Life Sciences are partnered with pharmaceutical manufacturer based in Liverpool, recruiting a Process Technician for a 6-month contract position. This is a hands-on role supporting critical manufacturing operations, utilities, and materials handling within a highly regulated GMP environment. The role operates on a 2 days / 2 nights / 4 off shift pattern and is Inside IR35. Key Responsibilities Monitor plant equipment and systems to ensure compliance with environmental, GMP, and safety regulationsComplete GMP documentation accurately and in line with regulatory and legislative requirementsMaintain high standards of safety, quality, and housekeeping in accordance with site procedures and cGMP expectationsReport safety, quality, and compliance issues via incident, near-miss, and deviation reporting systemsWork collaboratively within a multi-functional team and liaise cross-functionally to support operational objectivesComplete all mandatory training and contribute to continuous improvement activities, including Lean, 5S, and waste reduction initiatives Role Requirements Experience working in a chemical, pharmaceutical, or biotechnology manufacturing environmentBackground in a process or engineering support roleAbility to work in a cGMP- and HSE-regulated environment with an understanding of FDA, MHRA, HSE, and Environment Agency requirementsStrong written and verbal communication skillsMechanical aptitude with knowledge of electrical and mechanical equipmentAbility to follow complex procedures and work effectively under pressure

A global pharmaceutical company are recruiting for the next campaign and will be recruiting for Process Technicians for Flu manufacturing. The roles we require talented, adaptable individuals who can operate to the highest possible standards with a strong focus on safety, quality and compliance. The successful candidates will be instrumental in the creation of a new, operational areas within Manufacturing. The role will involve 12 Hour Day and Night Shifts working 4 on 4 off Days or 2 days 2 nights 4-5 Month Role £20.36 to £22.15 When manufacturing 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. * Carryout final documentation review and sign off to ensure documentation is right first time. * Ensure compliance to Health and Safety regulations. Consistently demonstrating the behaviours necessary to create a safe working environment for themselves and their colleagues *Be able to update existing SOPs and MIs as and when required performing regular reviews and initiating new documentation as appropriate. *To actively maintain and promote a cGMP compliant culture, ensure that the highest standards of housekeeping and safety are applied within the area in accordance with CFR regulations and to apply the principles of Lean Manufacturing, Problem Solving, 5S ,Waste Elimination and Energy Efficient Activities in support of Continuous Improvement. * To maximise their individual contribution so that team objectives are achieved. To work as a team member, providing and receiving support feedback to team members and their team leader. To communicate and liaise with members of other teams, customers and suppliers in order to meet the business's objectives. To suggest solutions to issues which may arise. *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. To continue to develop new skills, competencies and behaviours to fulfil both current and future business needs. The role holder will be able to demonstrate the application of the skills required for their role. * To work in a safe manner in compliance with all pertinent UK legislation, mandatory policies, guidelines and site procedures for Health, Safety and Environment. Experience This is a fantastic career opportunity for individuals with a commitment to work and ability to learn. Previous experience of working in a manufacturing environment or Science Degree Basic knowledge of GMP * Basic mechanical aptitude or knowledge of electronic / mechanical equipment.Individuals with Science qualifications will be considered. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser https://candidate-privacy

Skilled Pharmaceutical Operative for Aseptic Processing Role in Speke Liverpool - 6 Month Contract - Aseptic Experience Essential The role holder will be a key employee in the manufacturing organization. They will operate and perform a broad range of varied work activities which support the team objectives. The purpose of the role is to support the manufacture of viral seed stocks for use in the Influenza Vaccine manufacturing process. To be considered for this role you must have experience in an aseptic environment. Duties 1.When manufacturing ensure that all Departmental SOPs and Ml's 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. Carryout final documentation review and sign off to ensure documentation is right first time. Ensure compliance to Health and Safety regulations. Consistently demonstrating the behaviours necessary to create a safe working environment for themselves and their colleagues Be able to update existing SOPs and Ml's as and when required performing regular reviews and initiating new documentation as appropriate. 2. To actively maintain and promote a cGMP compliant culture, ensure that the highest standards of housekeeping and safety are applied within the area in accordance with the Orange Guide and CFR regulations and to apply the principles of Lean Manufacturing, Problem Solving, 5S ,Waste Elimination and Energy Efficient Activities in support of Continuous Improvement. 3. To maximise their individual contribution so that team objectives are achieved. To work as a team member, providing and receiving support feedback to and from team members and their team leader. To communicate and liaise with members of other teams, customers and suppliers in order to meet the business's objectives. To suggest solutions to issues which may arise. 4. 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. To continue to develop new skills, competencies and behaviours to fulfil both current and future business needs. The role holder will be able to demonstrate the application of the skills required for their role. 5. To work in a safe manner in compliance with all pertinent UK legislation,mandatory policies, guidelines and site procedures for Health, Safety and Environment. 7. To contribute ideas and action in order to improve team, process and equipment performance. To support process improvement and uphold Values and Behaviours. 8. Support organisation change and process improvements. Skill / Experience Skilled worker with relevant experience in pharmaceutical, biotechnology sterile production. Preference given to candidates with technical training in a bio tech programKnowledge of GMP - In an ASEPTIC areaBasic mechanical aptitude or knowledge of electronic mechanical equipment.Ability to work in, training for, or practical knowledge of clean room environment operations.Relevant Experiences Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser https://candidate-privacy