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(Senior) Project Manager (m/w/d)

Role overview

Qualifications

  • Academic degree (e.g., MSc, Ph.D.) in chemistry, pharmaceutical sciences, analytical chemistry, or a related scientific discipline
  • 3 years experience in the development of pharmaceutical products, process development, or analytical services within international cross-functional organizations
  • Solid understanding of working within a highly regulated and/or safety-critical environment (e.g. GMP requirements)
  • 2 years experience in project management, managing internal and external stakeholders

Responsibilities

  • Manage complex, cross-functional projects across pharmaceutical development, analytical testing, and process scale-up
  • Develop, track, and maintain detailed project plans, ensuring CMC analytical and non-clinical milestones are delivered on time and within budget
  • Facilitate communication between scientific teams, regulatory affairs, and external stakeholders
  • Proactively identify technical, regulatory, operational and logistical risks

Key facts

Other skills

  • Timelines
  • Coordinating
  • Problem Solving
  • Organizational Skills
  • Communication

About the company

NVision Imaging Technologies logo

NVision Imaging Technologies

Medical Devices & Equipment

At NVision, we engineer quantum-powered medical imaging technologies that deliver deeper, more precise MRI data for researchers and clinicians. Our unique hyperpolarization device POLARIS enables fast, simple, scalable imaging of metabolism at the cellular level. With hyperpolarized MRI, we are paving the way for earlier detection, faster treatment assessment and better risk profiling in oncology, cardiology, neurology and beyond.

Company details

IndustryMedical Devices & Equipment
Company size51 - 200

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Job description

Your mission

We are seeking a Project Manager (m/f/d) with a technical background in chemistry, pharmaceutical development or analytical science to manage complex projects within our clinical programme.You will coordinate complex technical projects across internal teams and external partners, with responsibility for timelines, dependencies, risks and delivery against agreed quality standards.
Your responsibilities shall include but may not be limited to the following:

  • Project Management: Manage complex, cross-functional projects across pharmaceutical development, analytical testing, and process scale-up. Take a hands-on approach and directly support the delivery of work packages when required.
  • Timeline & Milestone Management: Develop, track, and maintain detailed project plans, ensuring CMC analytical and non-clinical milestones are delivered  on time and within budget.
  • Technical Coordination: Facilitate communication between scientific teams, regulatory affairs, and external stakeholders, translating technical discussions and challenges into actions, decisions and project plans whilst fostering sustainable relationships.
  • Risk Management: Proactively identify technical, regulatory, operational and  logistical risks. Work  with project leads and subject matter experts to define and implement mitigations, and escalate significant issues where required.
  • Process Excellence: Support the Head of Program Management in establishing and maintaining a robust PM culture.


Your profile

  • Academic degree (e.g., MSc, Ph.D.) in chemistry, pharmaceutical sciences, analytical chemistry, or a related scientific discipline.
  • > 3 years experience in the development of pharmaceutical products, process development, or analytical services within international cross-functional organizations. 
  • Solid understanding of working within a highly regulated and/or safety-critical environment (e.g. GMP requirements).
  • > 2 years experience in project management, comfortably managing internal and external stakeholders, driving multiple competing priorities, escalating risks, and facilitating decision-making through facts and figures.
  • Comfortable with a range of project management methodologies (sequential/ waterfall, agile etc.)
  • Proactive, highly structured,  and well-organized approach to complex project landscapes.
  • Strong analytical and quantitative problem-solving skills
  • Fluent English skills, fluent German skills are a plus


Why us?

  • Competitive compensation, including base salary and stock options (virtual shares)
  • Homeoffice options or relocation support
  • Annual health budget (Allianz bKV)
  • 30 vacation days 
  • Flexible working hours 
  • Key role in a highly advanced and fast-growing startup company
  • Ample opportunity for personal initiatives, openness to new ideas, and room for considerable personal impact
  • Impactful product promoting better understanding and treatment of disease
  • International and dynamic team, comprising over 30 different nationalities
  • EGYM Wellpass membership
  • Permanent employment contract, providing stability and long-term career growth opportunities
  • Enjoyable work atmosphere with an open-door and open communication mentality


Contact information

Any questions? Please contact:

Sandra SchΓ€rli 
Senior Talent Acquisition Manager
mail: careers@nvision-quantum.com

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Marcus Rivera

Chief Revenue Officer

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