Job DescriptionProcess Engineer Specialist - Tech Transfer NPINew exciting opportunities now exists on our Carlow Site for a Process Engineer to join the Process Engineering Group on site and report to the Technical Engineering ManagerOur new team member will serve as technical support for new product introduction (NPI) and commercial manufacturing and will participate and/or lead cross functional or single function teams including liaising with vendors or above site groups. You will typically have prior related work experience; ideally in manufacturing, preferably GMP Setting but we will consider applicants from other working environments as long as they have technology transfer experienceKnowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable but not a necessity for this roleOur Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.What you will do: Bring energy, knowledge, innovation, and leadership to carry out the following:Design/Author/Review/Approve/Execute qualification/validation documentation and process development studies in line with the standard approval processDesign/Author/Review/Approve/Execute Execution/development of change controlsContribution to Kaizen events as appropriateTechnical input into quality notification by authoring/reviewing/approving investigationsExecution of equipment/qualification validation programs; including re-qualification and re-validationSupport continuous improvement through Lean Six Sigma methodologiesPerform root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issuesServe as technical engineering representative for internal technical group discussions and represent technical Operations Carlow at global technical forumsDrive compliance of Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions, ensuring consideration of the impact on GMP and compliance and decisions made. Accountable for compliance via documentation completion, risk assessments, closing out corrective action, participate in audits and inspections and proactively highlighting any issues around complianceWork collaboratively to drive a safe and compliant culture in CarlowMay be required to perform other duties as assignedWhat skills you will need:In order to excel in this role, you will more than likely have:Bachelor's Degree or higher preferred; ideally in a Science, Engineering or other Technical disciplineMin 3 years experience ideally in manufacturing, preferably GMP SettingDemonstratable experience of leading technical related projectsEvidence of continuous professional development is desirableKnowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable but not a necessityKnowledge of regulatory/code requirements to Irish, European and International Codes, Standards and PracticesReport, standards, policy writing skills requiredEquipment and process validationSterile filling processes and equipmentProficiency in Microsoft Office and job-related computer applications requiredExcellent communication, presentation and interpersonal skills, to interface effectively with all levels of colleagues and with external customers in a team orientated mannerAt our company, we work at the forefront of science and technology to advance manufacturing excellence and R&D across our Irish sites and global company network. We're always looking to make a difference for people, patients, and communities – from Ireland to the world.Required Skills: cGMP Guidelines, Communication, Electronic Batch Records, Lean Six Sigma (LSS), New Product Introduction (NPI), Process Development (PD), Process Engineering, Process Optimization, Standard Operating Procedure (SOP) Writing, Sterile Manufacturing, Teamwork, Technical Writing, TroubleshootingPreferred Skills: Current Employees apply HERECurrent Contingent Workers apply HERESearch Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: RegularRelocation:VISA Sponsorship:Travel Requirements:Flexible Work Arrangements:HybridShift:Valid Driving License:Hazardous Material(s):Job Posting End Date:12/20/2025*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.