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      • tallaght, international
      • permanent
      • randstad financial services
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries. Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D.Responsibilities Lead and manage the Validation activities within the site including but not limited to thermal validation, irradiation validation, equipment validation, facility validation and process validation. Implement and continually improve the validation system in line with appropriate national, European and international good practice standards and the strategic objectives of the site.Develop and promote a programme of activities that create and sustain a culture of quality and ensure an ongoing focus on the efficiency and continued appropriateness of procedures. Investigation and review of OOS validation results. Reporting of all investigations in line with appropriate procedures.Advising as part of the site management team on Validation issues. Lead and manage the validation function through the effective provision of well-defined goals and objectives, leadership training, support and guidance, and performance management to ensure consistent sustainable performance.Build and utilise effective cross-functional relationships with key stakeholders including Manufacturing and Quality Assurance. Ensure that appropriate standard operating procedures and technical guidelines for quality management are developed, implemented, updated and communicated on an ongoing basis to the relevant parties.Execution of Validation Studies, developing protocols for execution, coordination of validation studies and reporting of results in an effective and timely manner.Develop systems to monitor the effectiveness of the validation system and issue relevant reports to measure and monitor performance.RequirementsMinimum 4 year's experience working in a validation environment.Experience in sterile finished product manufacturing is desirable.Knowledge of respective standards and good manufacturing practices.Excellent interpersonal and communication skills.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
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries. Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D.Responsibilities Lead and manage the Validation activities within the site including but not limited to thermal validation, irradiation validation, equipment validation, facility validation and process validation. Implement and continually improve the validation system in line with appropriate national, European and international good practice standards and the strategic objectives of the site.Develop and promote a programme of activities that create and sustain a culture of quality and ensure an ongoing focus on the efficiency and continued appropriateness of procedures. Investigation and review of OOS validation results. Reporting of all investigations in line with appropriate procedures.Advising as part of the site management team on Validation issues. Lead and manage the validation function through the effective provision of well-defined goals and objectives, leadership training, support and guidance, and performance management to ensure consistent sustainable performance.Build and utilise effective cross-functional relationships with key stakeholders including Manufacturing and Quality Assurance. Ensure that appropriate standard operating procedures and technical guidelines for quality management are developed, implemented, updated and communicated on an ongoing basis to the relevant parties.Execution of Validation Studies, developing protocols for execution, coordination of validation studies and reporting of results in an effective and timely manner.Develop systems to monitor the effectiveness of the validation system and issue relevant reports to measure and monitor performance.RequirementsMinimum 4 year's experience working in a validation environment.Experience in sterile finished product manufacturing is desirable.Knowledge of respective standards and good manufacturing practices.Excellent interpersonal and communication skills.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
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Mechanical Design Engineer? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!As the Extrusion and Food Process Engineer, you will be the first member of the Bioprocess Engineering group that will be responsible for the design and implementation of our clients first-of-its-kind manufacturing processes and facilities. This position will design, build, test, and scale-up mechanical process equipment for cold extrusion and other specialty process applications. The role will require a strong background in machine design with the ultimate goal of deploying this equipment in our future commercial-scale manufacturing facilities and bringing strategic differentiation to our production platform.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Identify and define process and system requirements by understanding and challenging product formulation and processing assumptions with the aim of implementing robust unit operations and increasing overall operational efficiency and effectivenessPartner with internal and external teams to solve technical challenges and identify opportunities for process improvement and cost savingsManaging relationships with strategic partners, engineering firms, equipment vendors and technology partnersSpecify project scope, timelines, resourcing and budget needsDevelop project capital requirements and objectives through creation of proposals and plans with breakdown structures (WBS)Track and complete projects by managing schedules, costs and specificationsSome travel may be required to collaborator and manufacturing sitesAdditional ad hoc duties as required by the companyExperience: Ability to apply mechanical engineering principles and computer-aided methods to machine design and fabricationMechanical aptitude and comfortable with working directly on mechanical equipmentEfficient Design of Experiments and statistical analysis of experimental and characterization/validation dataUnderstanding of aseptic techniques and control of microbial contaminationAbility to partner cross-functionally on proprietary process technologies, while also developing and leveraging successful external contacts and relationshipsProject engineering and managementStrong scientific and technical writing and presentations.Detail oriented with excellent verbal and written communication skillsInnovative and creative thinking and willing to challenge established methods and beliefsSelf-starter with a strong bias for action and ability for problem-solving and trouble-shootingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Mechanical Design Engineer? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!As the Extrusion and Food Process Engineer, you will be the first member of the Bioprocess Engineering group that will be responsible for the design and implementation of our clients first-of-its-kind manufacturing processes and facilities. This position will design, build, test, and scale-up mechanical process equipment for cold extrusion and other specialty process applications. The role will require a strong background in machine design with the ultimate goal of deploying this equipment in our future commercial-scale manufacturing facilities and bringing strategic differentiation to our production platform.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Identify and define process and system requirements by understanding and challenging product formulation and processing assumptions with the aim of implementing robust unit operations and increasing overall operational efficiency and effectivenessPartner with internal and external teams to solve technical challenges and identify opportunities for process improvement and cost savingsManaging relationships with strategic partners, engineering firms, equipment vendors and technology partnersSpecify project scope, timelines, resourcing and budget needsDevelop project capital requirements and objectives through creation of proposals and plans with breakdown structures (WBS)Track and complete projects by managing schedules, costs and specificationsSome travel may be required to collaborator and manufacturing sitesAdditional ad hoc duties as required by the companyExperience: Ability to apply mechanical engineering principles and computer-aided methods to machine design and fabricationMechanical aptitude and comfortable with working directly on mechanical equipmentEfficient Design of Experiments and statistical analysis of experimental and characterization/validation dataUnderstanding of aseptic techniques and control of microbial contaminationAbility to partner cross-functionally on proprietary process technologies, while also developing and leveraging successful external contacts and relationshipsProject engineering and managementStrong scientific and technical writing and presentations.Detail oriented with excellent verbal and written communication skillsInnovative and creative thinking and willing to challenge established methods and beliefsSelf-starter with a strong bias for action and ability for problem-solving and trouble-shootingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

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