Senior Scientist GMT

The Global Manufacturing Technology group is responsible for new product introduction, technology transfers, process validation, and continued process technical support to unit operations for the commercial manufacture of multiple processes in the Zoetis Tullamore facility. The successful candidate will be a key contributor to a dynamic and highly technical team and will be required to build collaborations with Process Development, Manufacturing, Engineering, Supply Chain, Quality Assurance, Quality Control and Global Regulatory groups. The position is accountable for the timely completion of technical transfer and process validation related milestones, PPQ, process monitoring and manufacturing support. Expertise in the design, control, and processing unit operations.- Lead & Support new product introduction, process technology transfer, process validation and the preparation of CMC documentation for regulatory filings. Owning and driving significant cross-functional scopes of work associated with the technical transfer of new products.- Accountable for delivery of technical documents, including protocols, reports and SOPs supporting the validation of the manufacturing process. Assists in evaluating process performance by comparing manufacturing data to historical data.- Provide technical support for commercial manufacturing process and manage team input to investigations and resolution of process deviations, root cause analysis, CAPAs, process improvements, change controls and preparation of regulatory filings.- Strong knowledge of cGMP compliance, site and regulatory agency requirements and provides process subject matter expertise for regulatory inspections and other interactions with regulatory agencies.- Participates in continuous improvement initiatives, action plans to implement operational excellence, and lean practices along with setting and maintaining department goals and metrics.This role will include working with teams, both in Zoetis Tullamore and externally with Contract Manufacturing Organisations.The role will involve interaction with USP, and DSP teams within the manufacturing department and with external stake holders such as QC, WHSE and ENG.The role will require strong interaction with QAThis role involves building effective working relationships with other functional organizations, such as Process Development, Manufacturing, Quality Assurance, Quality Control, Engineering, Supply Chain, Regulatory, and others, both internally and externally to the site.Full timeLegal statement as belowThis job advert indicates the general nature and level of work expected. It is not designed to cover or contain a comprehensive listing of activities or responsibilities required of the incumbent. Incumbent may be asked to perform other duties as required. Additional position specific requirements/responsibilities are contained in approved training curricula. Visa status re must be eligible to work and live in Ireland as belowColleague must be legally eligible to live and work in Ireland.Summary of our Benefits In addition, to being part the world leading animal health company focused on the needs of those who raise and care for animals we offer a range of benefits such as competitive salary, bonus, 25.5 days holiday per annum plus public holidays, a defined contributory pension plan, private medical insurance for you and your family and empowered flexible working, to name a few.