Sr. Project Specialist

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?     There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.     We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.   Job Summary

In this fully onsite role, the Sr. Project Specialist will be responsible for managing the project management process for multiple complex projects simultaneously to meet internal and external customer deliverables.    The Sr. Project Specialist will also be responsible for driving projects to completion based on timelines, budget, and resources.  They will collaborate with R&D, Engineering, Procurement, Marketing, Quality, Regulatory, Product Management, Supply Chain, and other team members to manage and prioritize activities based on risk impact to the project.  They may evaluate, design, and implement efficient business processes across various departments, analyze workflows, identify areas for improvement, and develop strategies to enhance operational efficiency. They will support injection molds and/or automated assembly equipment programs. Essential Duties and Responsibilities

Communicate and provide project management activities for an operating unit, which may include internal and external partners and technical discussions. Build and maintain critical path, milestones and overall program timeline and budget. Responsible for coordinating with cross-functional team and external partners to implement improvements and monitor effectiveness. Document project team meetings and follow up on open action items. Proactively identify opportunities for continuous improvement. Create and maintain project documentation to communicate status and progress. May need to create flowcharts and process maps in Visio, standard operating procedures (SOPs), and other relevant materials. Conduct thorough analysis of existing processes to identify inefficiencies, bottlenecks, and initiate project change alerts in the case of delays, changes in scope, or deliverables. May need to identify areas of automation. Facilitate after action reviews as appropriate to identify successful and unsuccessful project elements. Attend tradeshows and other industry gatherings, as appropriate. May need to conduct business process mapping sessions with global teams to understand and document current business practices, and foster strong relationships with key stakeholders to ensure a collaborative approach to process improvement. May need to utilize data-driven insights to drive harmonization of different approaches, and develop strategies to ensure consistency and efficiency in operations. May need to partner with Process Owners to develop implementation roadmaps, develop training materials, provide support, and ensure that team members understand and adhere to new processes. Other duties as assigned. Education

Bachelor's Degree in Chemistry, Biology, Engineering or in another science related field, or equivalent experience required. Work Experience

Minimum 5 years  of professional experience in program management or project engineering within the medical device