Principal Program Lead Pharma Biotech

To support the business interests of NSF Health Sciences division, we are currently looking for a Principal Program. They will provide critical support to the Global Pharma Biotech Consulting and Training Team, within the Health Sciences Division to develop proposals for large projects (>$2m, typically) such as remediation projects, ensuring profit expectations are achieved. 

• To develop proposals for large projects (>$2m, typically) such as remediation projects, ensuring profit expectations are achieved.
• Manage >$5m worth of projects per annum. To manage the delivery of multiple projects, via employees and Independent Consultants
• Development of client deliverables Ø Selection and recruitment of resources (mainly Independent Consultants) to deliver the projects
• Ensure projects are managed effectively to meet time, cost, margin and quality expectations
• Work closely with clients via stakeholder reviews Develop and maintain client relationships to be the first point of contact for additional work. Expand project opportunities and revenue through existing client relationships.
• Showcase the work NSF does via white papers, webinars, speaking engagements at conferences.

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• Bachelor’s or Master’s Degree in Science, Technical or Engineering.
• 15+ years experience within Pharma or Biotech or Medical Device industry, or as a regulator to those industries.
• The experience must be linked to highly regulated markets such as the US FDA, EMA, or similar.
• 5+ years experience as a consultant to the relevant industry.
• Excellent presentation skills: ability to interpret and present highly complex and strategically significant information.
• Proactive with strong communication and negotiating skills both internally and in client facing situations.
• Strong focus on client engagement and client satisfaction, acting as the voice of the client during internal project management activities.
• Excellent verbal and written communication skills in English, bi-lingual proficiency highly preferred.
• Project management skills, an ability to manage multiple complex projects.
• Required to frequently travel both in the USA and internationally, up to 50-75% as per project requirements.

NSF is a growing global public health and safety organization. Our mission is to protect and improve human and planet health by enabling safe food, clean water and life-enhancing health technologies and products for millions of people around the world. We do so by developing standards, testing, auditing, certifying, and providing advisory services to clients in the food, water, health sciences and consumer industries.

Our nearly 3,000 employees provide services in over 180 countries through many of our global offices, at our 35,000 client sites, from home offices and in state-of-the-art laboratories. We’re growing fast and expanding into new areas such as sustainability and digital. And that’s where you come in. Come join a team that makes a difference in the world.

More information about NSF can be found at nsf.org

One of our core values is We Are One NSF. This means that while we’re one team, we embrace the cultural, ethnic, language and demographic diversity that reflects the societies in which we live and work. NSF is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, religion, sex, sexual orientation, gender identity, national origin, age, status as a protected veteran, or disability.

NSF works with pharmaceutical, dietary/nutritional supplements and personal care products, medical devices and in vitro diagnostic companies, large and small, to provide highly customized end-to-end services throughout the product lifecycle, from clinical trials to post-market surveillance. We are a global provider of clinical trials, training, consultancy, certification and auditing services to the health sciences industry. We have an outstanding international reputation in quality management and regulatory compliance. We provide comprehensive solutions for the health sciences industry from experts you can trust. Our team includes former FDA, EU and MHRA regulators as well as industry experts. We combine regulatory knowledge with industry best practices to provide our clients with tailored quality, compliance and regulatory services

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