Position SummaryThe Global Manufacturing Technology group is responsible for new product introduction, technology transfers, equipment and 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 equipment qualification, technical transfer, and process validation related milestones, PPQ, process monitoring and manufacturing support. Expertise in the equipment, utility, and facility validation.Position ResponsibilitiesDefine, execute, and report qualification, re-qualification, and validation studies in order to establish and maintain the qualified/validated status of range of status of facilities, utilities, and equipment in accordance with internal procedures, regulatory requirements, and industry guidance/standards. Provide technical expertise for investigation and compliant resolution of non-conformances encountered during requalification, revalidation, and periodic review activities (with support from senior validation team members). Advise systems owner and vendors on suitability and required standards/functionality of new systems during the selection process. 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.Organizational RelationshipsThis 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 QA. This 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.Resources ManagedN/AEducation and ExperienceBSc, MSc, or PhD, in a relevant discipline (e.g., biochemistry, chemistry, pharmaceutical science, biology, engineering) or equivalent experience.3+ year’s experience in pharmaceutical manufacturing organization and/or bioprocess development, with experience in upstream unit operations, process scale up, facility fit and process validation.Experience with large scale manufacturing support for mammalian cell culture, upstream and downstream processing, Single Use Systems, cGMP, and US / EU regulations.Excellent verbal & written communications skills. Interpersonal and facilitation skills necessary to interface with and influence all levels of the organization with the ability to lead people and multi-disciplinary teams.Project management capability.Ability to work effectively as part of a team across all departments in Zoetis Tullamore.Knowledge of quality systems, Quality by Design, validation principles for equipment, utility, and facility.Technical Skill RequirementBe proficient in ETS, SAP, Veeva Vault, strong knowledge of Excel, Word, and PowerPoint desirable.Strong strategic and analytical thinking, problem solving and rapid decision-making skills.Demonstrated capability in implementing challenging goals, objectives, and practices in a complex and ambiguous/matrix environment.Understanding of project management systems and tools. Management of multiple projects and timelines concurrently. Ability to adhere to standard timeline and escalate actions appropriately for resolution in a timely manner.Experience in qualification of, upstream and downstream processing equipment.Physical Position RequirementsThis role is primarily office-based with occasional out-of-hours support.This role may require periods of extended hours or a modified work schedule and may require on-call availability.Full timeRegularColleagueAny unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.