divh2Program Manager / h2pLocation : Onsite / ppStatus Type : Full Time / ppQualifications : / ppstrongRequired : / strong / pulliBachelor of Science in Engineering or Life Science / liliMinimum 8 years of experience in a regulated industry, preferably at least 3 years in medical devices, pharmaceuticals, and / or combination products / liliExperience in product or process development activities / process / liliMinimum 3 years of experience leading cross-functional, matrixed teams; experience managing external customers / clients preferred / liliExperience directly managing resources, budget, milestones, and detailed activities for large-scale projects / liliExperience managing people directly preferred / liliExperience directly managing customers, partnerships, alliances, or external contracts preferred / liliExperience in additional functional areas (e.g., quality, regulatory, human factors, manufacturing, or engineering) preferred / liliExperience working directly with ISO, FDA, MDD, and / or other healthcare industry regulations and standards / liliProficiency utilizing Microsoft Office suite (Word, Excel, PowerPoint, Project) / li / ulpstrongPreferred : / strong / pulliManage integration across companies for co-sponsored projects / liliMaster of Business Administration (MBA) or Master of Science in Engineering / Life Science (Preferred) / liliProject Management (e.g., PMP or CAPM) Certification (Preferred) / liliKnowledge of regulatory requirements governing drug and device development, human factors, commercial manufacturing operations, regulatory approvals and / or product launch experience / liliPMP or CPM / li / ulpstrongSkills Competencies : / strong / pulliLeads cross-functional team, including driving accountability and responsibility for results and forward progress / liliCollaborates effectively with diverse stakeholders; demonstrates partner commitment and customer orientation / liliCommunicates effectively in writing, including ability to write in a clear, concise, logical, and grammatically correct manner / liliSeeks to understand when listening to others; demonstrates awareness of what is requested; communicates orally in a professional manner that inspires confidence / liliExercises discernment in dissemination of information and sense of urgency; escalates issues to ensure timely and relevant responses; demonstrates ability to handle sensitive information with discretion and tact / liliDemonstrates high attention to detail; conveys excellence in partner deliverables / liliDistills complicated topics for intended audience; facilitates large discussions, and adjusts / adapts / responds to real-time feedback / liliLeads and executes strategic plans and workstreams, including planning, organizing, securing, and managing resources to achieve goals / liliSolves problems, including providing clarity in defining problem statements in ambiguous, complex situations; draws logical conclusions / liliSets clear goals, delegates effectively, and leverages the skills and expertise of others / liliInfluences without direct authority; maintains rational and objective demeanor when faced with stressful situations / li / ulpstrongPhysical Requirements : / strong / pulliAbility to remain in stationary position for extended periods of time / liliAbility to consistently operate a computer, and other office equipment (e.g., printer, telephone, etc.) / liliAbility to work in an open office environment, on-site at an Enable location / li / ulpResponsibilities : / pulliManage drug partner program(s) and project(s) from inception through commercial launch and life-cycle management (i.e., product retirement); develop, track, analyze and communicate key performance indicators on the program, including the effectiveness of technical strategies, regulatory pathways, clinical build progress, project execution, and product development risks (e.g., alignment to schedule, scope, resources) / liliSupport all phases of the product development process from Concept to Launch; understand Design Control principles and support gate-keeping, design freezes, design reviews, change control, sign-offs, etc. / liliImplement best practices on programs / projects; ensure consistency and thoroughness of deliverables throughout program / liliDevelop, maintain, and nurture positive relationships with key stakeholders at pharmaceutical partners; serve as key contact for program; establish credibility with pharma partner / liliDevelop, maintain, and nurture positive relationships with internal colleagues; demonstrate high level of interpersonal skills in interactions; work independently with limited oversight / liliLeverage team skills and experience to achieve program / project goals; communicate clear expectations to team members in order to meet deadlines / liliIdentify business and process issues; model a culture of quality and continuous improvement / liliMaintain awareness of new and changing processes on programs / projects; identify potential risks for pharmaceutical partners; implement necessary changes to maintain compliance / liliModel teamwork, diversity, and inclusion within team, between teams and other groups / li / ul / div
Program Manager • Cincinnati, OH, US