[1/28/2025 A] QA Specialist

13 hours ago


Dublin, Ireland PE Global Full time

The Role: PE Global are recruiting for a Manufacturing Specialist Investigations Lead to be based in Dun Laoghaire 12 Month initial contract - Hybrid Good technical writing for all deviation incidents, the team must write a thorough write up. So, the candidate must be comfortable with writing clear information and ensure it is detailed. Good project management skills for every deviation incident it will require the CW to manage timelines and expectations. Strong Communication this goes hand in hand with the technical writing as the CW will lead cross functional teams who may not have the technical knowledge. So the CW will need to ask the right questions and get the right information from people. Somebody with a Specialist QA background is suitable for the role. The team may not be in QA, but theres a lot of compliance in place. Description: The Manufacturing Specialist (Investigation Lead) will be primarily responsible for leading investigations for fill/finish/inspection and packaging deviations. Specialists will also be involved in applying process, quality, compliance, and analytical knowledge to complete the following: Manage deviation investigations, including establishing investigation teams, leading root cause analysis, development of CAPAs, completing product impact assessments and writing comprehensive compliant documentation of all findings. Clear and concise technical writing of complex investigations Drive improvements to the investigation process Present investigations to regulatory inspectors and internal auditors Clearly communicate investigation progress to impacted areas and leadership Coordinate and lead cross-functional teams through complex investigations, and complete tasks on-schedule. Project management of the investigations end to end Present complex topics to large and small groups at various levels and quickly understand and clearly communicate complex issues. Build effective relationships across functions. Navigate through ambiguity and provide a structured problem-solving approach. Able to apply inductive and deductive reasoning in the investigation process Qualifications: Bachelor's Degree in Science or Engineering and 5+ years of directly related experience in a biotech/pharma manufacturing or manufacturing support role (ie process development, engineering, quality) OR * Associate's Degree in Science or Engineering and 8+ years of directly related experience in a biotech/pharma manufacturing or manufacturing support role (ie process development, engineering, quality) * 10+ years directly related experience in a biotech/pharma manufacturing or manufacturing environment Detailed technical understanding of fill/finish operations Experience with compliance, problem-solving, root cause analysis, critical thinking, project management, and quality systems. Experience leading complex investigations Experience participating in and leading cross-functional teams Experience in managing multiple, competing priorities in a fast-paced environment Experience presenting to inspectors during regulatory inspections and internal audits. Excellent technical writing Excellent presentation and communication skills, ability to communicate and collaborate with technical and management staff Ability to be flexible and manage change Interested candidates should submit an updated CV. Please click the link below to apply, call Audrey Mccarthy on or alternatively send an up to date CV to 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: manufacturing investigations deviations



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