Validation Specialist Officer (Senior Role)- Parma area Italy

ph3About Us /h3 pProductLife Group (PLG) is a dedicated life sciences and pharmaceutical outsourcing and consulting company providing expertise and services in areas such as: Product Development, Market Patient Access, Regulatory Affairs and Safety Vigilance as well as Engineering and Digital Transformation.The group has its HQ in Paris and affiliates around the globe with teams in all key regions: North America, Europe and APAC. /p pWe are now on the look out for an experienced Validation Specialist Officer to enhance and join PLG Center of Expertise Engineering (previousl y CP Engineering). Our Center of Expertise, is a multidisciplinary engineering and consulting firm specializing in providing tailored solutions for the pharmaceutical, medical, nutraceutical, and cosmetics industries in areas such as Engineering, Construction, Qualification Validation as well as Energy Waste Management. /p pThe job location is around Parma in Italy with a hybrid working policy. /p h3About The Job /h3 pYou will have ownership of the following activities supporting our clients' Qualification Validation Opeeations: /p ul liPlan, execution, and documentation of qualification and validation activities (IQ/OQ/PQ) for facilities, utilities and equipment /li liPreparation and review of validation protocols, reports and related documentation /li liCoordinationn of qualification and validation activities, ensuring timely execution and documentation review /li liEnsure compliance with GMP requirements and internal quality standards /li liSupport change controls, deviations, CAPAs, and risk assessments related to validation /li liCollaborate with clients cross-functional teams (QA, Production, Engineering, QC) to support validation projects /li liMaintain validation documentation and ensure the validated state of equipment and processes /li lidrafting Validation Master Plan /li lirisk analysis /li lidrafting SOPs /li /ul h3Required Skills And Experience /h3 ul liBachelor's/ Master's degree in Engineering, Life Sciences, Chemistry, Pharmacy, or a related discipline. /li li3+ years relevant professional experience /li liExperience in Facility, Utility, and Equipment Qualification and Commissioning within a GMP-regulated environment. /li liStrong technical writing skills, with the ability to prepare clear, accurate, and compliant qualification and validation documentation /li liExperience in drafting qualification protocols, reports, SOPs, and other GMP documentation /li liGood understanding of GMP requirements and validation principles. /li liProficiency in Microsoft Office 365 (Word, Excel, PowerPoint, Outlook). /li /ul h3Additional Skills /h3 ul liStrong attention to detail and commitment to quality /li liTeam coordination or leadership experience /li liExcellent teamwork and collaboration skills /li liStrong analytical and problem-solving abilities /li liGood interpersonal and communication skills /li liClient relationship and stakeholder management experience /li liFlexibility and willingness to travel to client sites as required /li /ul /p #J-18808-Ljbffr