Global Project Manager

About the Role

Key Responsibilities

• Own and implement project/program/product structures for product development and product care activities including communication management, timelines, resource and budget plans, progress and cost control.
• Create, coordinate, and maintain integrated project plans including dependencies, resources, and budgets to enable efficient and effective team work.
• Be accountable for quality implementation in projects, including project risk management, critical path analysis, scenario creation and analysis, budget management, and robust planning.
• Execute project management processes such as guiding preparation for milestone reviews and capacity reviews, and lead improvement initiatives.
• Apply and coach teams in agile methods and project methodology, including hybrid Agile approaches combining Agile and non-Agile techniques.
• Lead meetings, foster knowledge sharing, and establish positive team dynamics through team building.
• Set goals, establish, measure, and report KPIs, OKRs, or OBPs to enable teams to measure and improve quality, efficiency, and effectiveness.
• Serve as a single point of contact and control for project and program data, acting as a trusted advisor for holistic planning and risk management.
• Identify project risks, describe potential implications, challenge assumptions, propose innovative options, and communicate issues proactively to stakeholders.
• Manage project/product team information to support decision-making and act as an Agile Program Manager as defined by SAFe where applicable.
• Work closely with various leads and partners to ensure optimized project delivery, coach team members, and develop new skills.
• Lead improvement initiatives including proposals, planning, and implementation at Sub-Chapter or Chapter level.

Requirements

• Bachelor's degree in science, engineering, or business from an accredited institution.
• 6-8 years of project management experience in diagnostics, medical devices, pharmaceuticals, or biotech.
• 1-3 years of experience in clinical biomarker or In Vitro Diagnostic development.
• Experience in a regulated industry, strong problem-solving and conflict management skills.
• Profound understanding and knowledge of relevant Design Control and/or Phased Development processes.

Nice to Have

• Master's degree in science, engineering, or business related fields from an accredited institution.
• Demonstrated experience with Agile development practices and mindset.
• PMP Certification and SAFe Certification.

Qualifications

• Bachelor's degree in science, engineering, or business.

Benefits & Perks

• Relocation benefits are available.
• Expected salary range of $100,000 to $185,600 based on location and experience.
• Discretionary annual bonus based on individual and company performance.
• Position qualifies for benefits detailed at the provided link.