Technical Transfer specialist
19 hours ago
The Role: This position will provide technical support to the Vaccines IPT to support the technology transfer and scale-up of new processes for Vaccines IPT manufacture meeting the Manufacturing Division Priorities of: Compliance, Supply, HPO, Strategy and Profit Plan. Responsibilities: Ensure the highest Quality, Compliance and Safety standards primarily with Technology Transfer but relating to all activities. Work within a team to enable the teams performance within the Vaccine Technology Transfer group in the Technical Operations Dept. Responsible for the technical transfer and scaleup of a new process into Vaccines IPT. Input into Technical planning and decisions for the Vaccines IPT, to ensure supply of high quality product through tactical planning and execution of production schedules. Technical Review, ownership of and approval of Change Control, Quality Notification, deviation and investigation records as required. Recommend technical approaches in line with global and local standards. Benchmark and remain current with development of new technologies in the vaccine and biopharmaceutical processing field of expertise and seek to deploy process improvements through innovation and utilization of these technological advances. Contribute for driving a culture of Continuous Improvement by deploying MPS within the IPT on projects such as: problem solving, reducing cycle time, Lean principles within the new processes. Stakeholder management of multiple decision makers, corporate colleagues, cross-functional team by demonstrating the ability to maintain and strengthen trust relationships with people on all levels Participate and comply with the MMD Quality Management System (QMS) requirements, including ownership, as relevant. Requirements: 4 years experience in biopharmaceutical/vaccines environment Demonstrated knowledge in pharmaceutical / biopharmaceutical technical / manufacturing operations. Experience of involvement in a technical project an advantage Knowledge of Regulations and applicable standards for Quality, Safety, Regulatory within the biopharmaceutical/vaccine area. Qualifications: Hon. Degree or Masters in a Science or Engineering discipline (preferably Biotechnology). Preference for Lean Six Sigma qualification or experience of application of Lean principles Project management qualification such as, Project Management Professional is desirable Evidence of Continuous Professional Development Skill Set: Demonstrated knowledge in more than one pharmaceutical or Biopharmaceutical manufacturing operation (e.g. manufacturing, technology, validation, engineering, quality.). Demonstrated ability in holding project team members responsible for results and being decisive about non-performers. Demonstrated ability to realize improvement initiatives. Demonstrated successes in a team environment, such as project teams. Demonstrated high level of problem solving and facilitation skills. Advanced PC skills such as Excel, Word, PowerPoint. Stakeholder management of multi decision makers, colleagues, peers and cross functional teams. Experience in a FDA / HPRA Regulated production environment. Interested candidates should submit an updated CV. Please click the link below to apply, or alternatively send an up to date CV to ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland*** Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert. Skills: Tech Transfer Change Control Deviations
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Senior Technical Transfer Specialist
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Cork, Ireland Recruitment by Aphex Group Full timeThis is an 11-month initial contract. Purpose A fantastic opportunity has arisen for a Senior Technical Transfer Specialist to join our growing Engineering team. You will lead, collaborate and facilitate running of activities (e.g. scale-up, PPQ batch manufacture, license submissions, technical troubleshooting and audit readiness) for Technology Transfer of...
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Cork, Ireland Recruitment by Aphex Group Full timePurpose This position will provide technical support to the Vaccines IPT to support the technology transfer and scale-up of new processes for Vaccines IPT manufacture meeting the Company Priorities of: Compliance, Supply, HPO, Strategy and Profit Plan. Responsibilities The Specialist will be required to lead, collaborate and facilitate running of activities...
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▷ Apply Now! Senior Tech Transfer Specialist
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