Job Description

Work Schedule Standard (Mon-Fri)
Environmental Conditions Office

By leading collaborative cross-functional teams to define and deliver commitments: demonstrating feasibility for new technologies, commercializing new products, or improving on-market products, all using our stage-gate or iterative processes to deliver to the agreed scope, schedule, and budget, while managing execution, risks, trade-offs, expectations, and communications.
What will you do?

• Lead programs and projects, negotiating trade-offs, determining and committing to the right scope, schedule, and budget to deliver winning business results.
• Drive and track all day-to-day project work, making sure that problems are rapidly identified and resolved, applying state-of-the-art project management tools and techniques to deliver on commitments and in some instances adhere to specific regulatory requirements.
• Lead project communications and phase approval reviews, providing clear and concise written and verbal communication to all levels of the project team and stakeholders, and tailoring style to a broad range of audiences and situations.

Education/Experience:

• Bachelor's degree in Biology, Chemistry, Physics, Engineering or Life Science required; PMP certification, advanced leadership training, MS, MBA or Ph.D. preferred.
• 10+ years of life science or medical device product development and 5+ years technical project management experience required; experience with genetic analysis technologies and in-vitro diagnostics preferred.
• Fluent in English.

Knowledge, Skills, Abilities:

• Intrinsically motivated, accountable, and committed to professional development.
• Excellent written and verbal communicator; exceptional relationship builder.
• Effective at influencing and leading without direct authority.
• Ability to lead and drive complex decisions and solve problems.
• Strong product development technical and business expertise.

Skills Required