Sr. Project Manager - Technical Services

Meeting Minutes/Agendas Job Title Sr. Project Manager, Technical Services Location Columbus, OH Job Type Full time Req ID 11031 About Us As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ mission is to bring Better Health. Within Reach. Every Day.® for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 800 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our 32 manufacturing plants, eight R&D centers, and 9,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them accessible to the people who need them. Description We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Sr. Project Manager, Technical Services to join our team. In this role, you will be responsible for will lead and manage cross-functional project teams for products produced or distributed from Columbus either via launch, transfer and/or lifecycle. This position is responsible to provide all necessary project management skills/tools for the successful, timely completion of all assigned projects in order to achieve the site’s goals for each year with key performance indicators being timing, cost and process robustness. This role has full accountability for the planning and execution of Generic commercialization, Site Transfers, Buy-ins, Third Party, Alternate API, process changes (Quality & Product Robustness driven) and changes to Active Pharmaceutical Ingredients, Excipient, Packaging and Raw Material items. Key Responsibilities Manages and delivers organizational and project leadership for Generic commercialization, Site Transfers, Buy-ins, Third Party, Alternate API, process changes (Quality & Product Robustness driven) and changes to Active Pharmaceutical Ingredients, Excipient, Packaging and Raw Material items. Proactively identifies & manages risk which could adversely affect successful project completion. Lead & facilitate multiple cross-functional team by managing and directing project team resources / experts to identify relevant issues and effectively manage progress and change. Ensures integration of technical/commercial information and activities necessary to develop and support the success of the plan by utilizing project management skills/tools, including but not limited to, to successfully drive the project to meet established timelines: Project Plan Meeting Minutes/Agendas RAID log Costing assessments Meeting facilitation (Core & relevant sub‑teams) Assesses critical data and contributes information to identify / facilitate critical "Go / No Go" project decisions. Provide proactive communication to all stakeholders, regarding issues, risks, contingency plans and potential negative impacts to the established milestones and timelines. Be change leaders ensuring change management requirements are being facilitated i.e. Initial change notification assessment (SME assessment, cost evaluation, Master Change assessment) Management of Tactical and Strategic change meetings Creation of required Protocols (Change & Master Change) Creation of Qualification Technical Reports Management of CC’s in appropriate system Stage/Que/Monitor work in‑progress Develop/Manage implementation plan Ensure Document review prior to final implementation Assess completed projects for lessons learned to drive improvement in project performance/execution and capture data to drive/refine resource allocation/costing for future projects. Mentor and develop other members of the Technical Services department. Act as a subject matter expert on core technologies and/or project management topics (e.g. meeting facilitation, influence, risk management, etc.). Lead knowledge sharing, individual skill development, and career development within the department, through sharing and implementation of best practices in both individual and group settings (e.g. 1:1 mentoring regarding a specific product/process challenge, and in PC meetings/staff meetings, respectively). Identify and proactively create opportunities to mentor/job shadow with Junior Project Managers on specific equipment and process technologies (e.g. bringing Junior Project Managers to the shop floor during production and/or troubleshooting support), and on project problem solving (e.g. risk mitigation of various end to end supply chain trends of potential concern during peer review of a Junior Project Manager’s project, provide mentoring on recommend approaches for analysis and remediation, if needed). Lead skill development of Junior Project Managers in the competency of Planning/Organizing, Critical Thinking, Problem Solving/Resolution, and Influence. Qualifications We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them: B.S. degree in a scientific and/or related operations discipline plus a minimum of 9 years’ experience in pharmaceutical (multi‑disciplinary experience: change management, analytical and/or drug regulatory affairs preferred) and/or project management. Alternatively, a M.S. degree in a scientific and/or related operations discipline plus a minimum of 7 years’ experience in pharmaceutical (multi‑disciplinary experience: change management, analytical and/or drug regulatory affairs preferred) and/or project management. Minimum 9 years of industrial multi‑disciplinary experience managing multiple, complex projects and/or implementing continuous improvement. Expert knowledge and understanding of applicable regulations pertaining to the development and manufacturing of pharmaceuticals including cGMP, DEA, and FDA, EMEA. Must possess knowledge of SOP’s, production processes and equipment and have strong understanding of pharmaceutical supply chain operations, business analysis, and pharmaceutical technology. In addition, demonstrated knowledge of pharmaceutical development, scale-up and validation, and lifecycle processes. Expert knowledge and understanding of project management methodology with an active PMP certification with the ability to effectively manage and partner with subordinates, peers, suppliers and contractors. Demonstrated ability to deliver on results to meet determined business objectives/targets. Demonstrated ability to communicate effectively (oral and written) both internally and externally at various levels locally, regionally & globally Demonstrated knowledge in continuous improvement methodologies and implementation with an active six‑sigma certification preferred. Competencies Critical Thinking: Ability to work in uncharted areas; capable of integrating large amounts of information to address complex issues. Challenges conventional wisdom when required. Intellectually aggressive with a strong end‑product orientation. Complex Problem Solving: Expert knowledge and ability to apply investigative techniques to uncover problem areas, determine root causes, and drive corrective actions at both the individual and cross‑functional team level. Uses problem solving abilities requiring attention to detail, accuracy, and scientific judgment. Develops solutions to a variety of problems of high scope and complexity, as defined in Accountabilities section. Project Management: Experience managing and leading projects and/or process improvements teams of high scope and complexity. Initiative: Works independently on activities ranging from strategic decisions to tactical execution of tasks with high complexity. Exercises latitude in determining objectives and approaches to assignments. Organizational Skills - Able to operate independently. Manages time well, follows through on commitments and pays attention to details. Able to work on several projects simultaneously. Teamwork: Demonstrated ability to be influence team members and senior leaders on topics of high complexity, and to lead/facilitate teams on tasks of high complexity. Coaching/ Mentoring/Influencing: Strong ability to coach and/or mentor/influence both in and out of reporting structure. Foster the professional development by willing sharing of personal knowledge and experience enabling individuals and teams to higher levels of performance. What We Offer* Annual performance bonus, commission, and share potential Auto enrollment in a Hikma-sponsored 401(k) program at a pre‑tax contribution rate of 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries 3 personal days (prorated based on hire date) 11 company paid holidays Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits Employee discount program Wellbeing rewards program Safety and Quality is a top organizational priority Career advancement and growth opportunities Tuition reimbursement Paid maternity and parental leave Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms. Equal Opportunity Employer Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law. #J-18808-Ljbffr Hikma Pharmaceuticals