Validation Project Managers

Validation Project ManagerWork Your Magic with us! Start your next chapter and join EMD Serono.Ready to explore, break barriers, and discover more? We know you've got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.Job Site: 400 Summit Drive Burlington, Massachusetts 01803 Telecommuting: At least three days of in-office work per week are required, so the individual must reside in the Burlington, MA area.Responsibilities:The responsibilities of the Validation Project Manager include: Manage multiple customer projects – including bacterial retention testing, physical testing (compatibility, product bubble point/diffusion, and/or Vmax) and extractables and leachables – from order to final report, ensuring successful completion; Develop realistic project plans shared with customers, monitoring progress and adjusting timelines as necessary; Serve as the liaison between customers and validation service teams to coordinate activities effectively; Communicate proactively with customers and internal teams through timely updates, meetings, and discussions; Create, update, track, and close projects accurately and in a timely manner; Provide adequate level of technical support for standard services. Help customers define their needs and answering basic questions; Consult with VPMs, laboratory experts, and support teams for necessary project information and assistance; and Assist with standard quotations based on customer needs and regulatory requirements while providing technical support.Requirements & Qualifications:The employer requires a bachelor's degree in Biology, Biochemistry, Chemistry or closely related field and at least two years of work experience in any occupation within the biotechnology or pharmaceutical industries. In addition, the employer requires the following: Demonstrated knowledge of extractables and leachable validation gained through at least two years of work experience; Demonstrated knowledge of project management and scheduling tools such as SalesForce, Smartsheet, SharePoint, and Microsoft 360 gained through at least two years of work experience; Demonstrated knowledge of quality assurance and Good Documentation Practices (OSHA, EHS, ISO9001) gained through at least two years of work experience; and Demonstrated ability working with root cause analysis gained through at least two years of work experience. All years of experience may be gained concurrently.Salary Range: $78,208 to $98,208 per year.

Compensation is based on experience, location, and other factors. We offer generous benefits packages.What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!