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    • tullamore, international
    • permanent
    • randstad financial services
    Position Title : Process ScientistDepartment : Development and ManufacturingLocation : Tullamore Role PurposeThe role of this key team member within the Development/Production Department will include responsibility for the development and validation of processes for recombinant proteins for veterinary use. This will include working with teams, both in their Tullamore site and externally with Contract Manufacturing Organisations for some of the process development activity, and technical transfer of the process into the client's facility in Tullamore. Duties & ResponsibilitiesHave significant knowledge of bioprocessing.Applies technical skills and functional knowledge independently and proactively. May act as a technical resource within their own group/team.Assist with decisions that impact your own work/ team group with the ability to make- decisions that may resolve moderately complex problems.Exercises judgement utilising established approaches as well as prior work experience, consulting others appropriately.Works under limited supervision and provides novel process solutions, new ideas and knowledge. Contributes to achievement of goals at the team level and takes responsibility for a portion of the team's milestones or deliverables. Proactively offers to investigate a problem using its own resources to resolve an issue.May provide training/ coaching/ mentoring within the work group/ team and supervise other colleagues.Influences at the work group and/or project team level.Modifies existing processes to improve the efficiency of the work group or function.To support the development, optimisation, scale-up and validation of all steps in the monoclonal antibody production process.Work with external service providers (CMOs) to provide the necessary technical support for successful completion of projects, including the transfer of the process into the site facility.Support the writing of Batch Manufacturing Records, SOPs, and other quality system documentation required for GMP manufacture.Provide hands-on technical support for all manufacturing activities, including buffer/media preparation, cell culture and purification processes.Provide technical input and support writing of technical reports required for regulatory purposes.Participate in Quality and Safety regulatory audits.Identify continuous improvement initiatives and action plans to implement operational excellence and lean practices.POSITION SPECIFICATIONQualifications, Experience, Skills, Knowledge and AttributesBSc, MSc, PhD in a relevant discipline (e.g. biochemistry, chemistry, process engineering) or equivalent experience.2-5 years' relevant experience in bioprocess development and/or manufacturingProtein purification, lab-scale and pilot scale.Knowledge of UNICORN programming is desirable.Lean six sigma certified. Skills with chromatography systems, filtration systems.Working in a controlled regulated environment e.g. GMP/GLP.Knowledge of analytical methods required for protein characterisation.Knowledge of key suppliers of process materials and equipment, including disposable systems.Experience working with external contractors.Excellent project management capability.Excellent verbal and written communication skills. Ability to maintain very clear records of work completed.Ability to work effectively as part of a team across all departments in their Tullamore site. Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
    Position Title : Process ScientistDepartment : Development and ManufacturingLocation : Tullamore Role PurposeThe role of this key team member within the Development/Production Department will include responsibility for the development and validation of processes for recombinant proteins for veterinary use. This will include working with teams, both in their Tullamore site and externally with Contract Manufacturing Organisations for some of the process development activity, and technical transfer of the process into the client's facility in Tullamore. Duties & ResponsibilitiesHave significant knowledge of bioprocessing.Applies technical skills and functional knowledge independently and proactively. May act as a technical resource within their own group/team.Assist with decisions that impact your own work/ team group with the ability to make- decisions that may resolve moderately complex problems.Exercises judgement utilising established approaches as well as prior work experience, consulting others appropriately.Works under limited supervision and provides novel process solutions, new ideas and knowledge. Contributes to achievement of goals at the team level and takes responsibility for a portion of the team's milestones or deliverables. Proactively offers to investigate a problem using its own resources to resolve an issue.May provide training/ coaching/ mentoring within the work group/ team and supervise other colleagues.Influences at the work group and/or project team level.Modifies existing processes to improve the efficiency of the work group or function.To support the development, optimisation, scale-up and validation of all steps in the monoclonal antibody production process.Work with external service providers (CMOs) to provide the necessary technical support for successful completion of projects, including the transfer of the process into the site facility.Support the writing of Batch Manufacturing Records, SOPs, and other quality system documentation required for GMP manufacture.Provide hands-on technical support for all manufacturing activities, including buffer/media preparation, cell culture and purification processes.Provide technical input and support writing of technical reports required for regulatory purposes.Participate in Quality and Safety regulatory audits.Identify continuous improvement initiatives and action plans to implement operational excellence and lean practices.POSITION SPECIFICATIONQualifications, Experience, Skills, Knowledge and AttributesBSc, MSc, PhD in a relevant discipline (e.g. biochemistry, chemistry, process engineering) or equivalent experience.2-5 years' relevant experience in bioprocess development and/or manufacturingProtein purification, lab-scale and pilot scale.Knowledge of UNICORN programming is desirable.Lean six sigma certified. Skills with chromatography systems, filtration systems.Working in a controlled regulated environment e.g. GMP/GLP.Knowledge of analytical methods required for protein characterisation.Knowledge of key suppliers of process materials and equipment, including disposable systems.Experience working with external contractors.Excellent project management capability.Excellent verbal and written communication skills. Ability to maintain very clear records of work completed.Ability to work effectively as part of a team across all departments in their Tullamore site. Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003

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