PE Global is recruiting for a Contract Development & Manufacturing Manager for our biopharmaceutical client in Dublin. This is an initial 12-month contract, hybrid role.Hybrid = Onsite 2-days per month.OverviewSeeking an external contract worker to join the External Process Development Organization initially for a 12 month period. The Contract Testing Laboratory (CTL) CW will work with CRO's/CTLs's to deliver on pipeline molecules. The CTL team will develop the external sourcing strategy for commercial and development portfolio for external contract testing laboratory. The CTL team is part of the External Supply organization is accountable for the execution of testing activities associated with the laboratory within scope.Position ResponsibilitiesLaboratory Supplier relationship management, including development and reporting of metrics and monitoring performance to continuously improve efficiency and effectiveness of suppliers. Building and maintaining strong partnerships with all external laboratory functions to increase overall effectiveness and success of programs. Ability to operate in highly matrixed teams.Project management of a portfolio of cross-disciplinary external projects traversing the areas of Drug Product, Drug Substance, and Attribute Sciences. Primary focus will be to manage delivery of analytical work packages (method qualification, method transfer, release testing, stability testing, characterization sample management ) with external contract laboratoriesActively participate in cross-functional teams with clear accountability for performance and ensure the quality, cost, and delivery of products from Contract Testing Laboratory sites are consistently met, as well as lead issue resolution, problem solving and serve as an escalation agent.Responsible to ensure analytical escalations are captured and communicated accurately and timelyIdentification of project optimization opportunities (timeline, budget, technical execution), prioritization of a rolling portfolio of projectsEnsure that designated lead programs meet compliance, speed, quality, and cost targets through strong scientific and technical understanding of the programs and drug product development.Identification of project optimization opportunities (timeline, budget, technical execution), prioritization of a rolling portfolio of projectsSupplier evaluation and selectionThis position will require occasional domestic and international travelDesired ExperienceEducationMaster's Degree & 2 years of Scientific experienceORBachelor's Degree & 3 years of Scientific experienceCore CompetenciesAdvanced degree in engineering or the sciences.Experience in large molecule analytical development including method development, method qualifications/transfers/validations, release, stability and characterization testing.Self-starter with a high-level of comfort with ambiguity and complexity and the ability to multi-task while consistently delivering quality resultsExperience interfacing with domestic and international CTL /CRO organizationsStrong understanding of cGMP, Regulatory/CMC, legal, Quality requirements and import/export policiesDemonstrated understanding of drug development and commercialization for synthetic and/or biologic therapeuticsExperience as team member/leader of cross-functional and matrixed teams including effective writing, presentation, organizational and interpersonal skills to address a broad scope of audiencesProven business acumen, high level strategic thinking, and strong analytical skills with the ability to structure, pragmatically scope, and solve complex problemsDemonstrated quantitative skills including experience in business process development, continuous improvement, operational excellence and performance managementInterested candidates should submit an updated CV.Please click the link below to apply, or alternatively send an up-to-date CV to ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***