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

Nvision Quantum; Lehr; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Benefits dieser Stelle

Stock options (virtual shares)

Homeoffice options or relocation

Annual health budget

30 vacation days

Flexible working hours

Permanent employment contract

Zusammenfassung

Nvision Quantum is 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 internal teams and external partners to manage timelines, risks and quality across the project portfolio.

You will lead cross-functional teams in pharmaceutical development, analytical testing and process scale-up, ensuring milestones are met on time and within budget.

Qualifikationen

• Academic background in chemistry, pharmaceutical sciences, analytical chemistry, or related field.
• >3 years in development of pharmaceutical products, process development, or analytical services in international settings.
• Strong understanding of working in regulated environments (GMP).
• >2 years in project management, coordinating internal/external stakeholders and prioritising multiple priorities.
• Familiar with sequential/waterfall and agile methodologies.
• Proactive, structured, and well-organized in complex landscapes.
• Strong analytical and quantitative problem-solving skills.
• Fluent English; German is a plus.

Aufgaben

• Manage complex, cross-functional projects across pharmaceutical development, analytical testing, and process scale-up; support delivery of work packages when needed.
• Develop, track, and maintain detailed project plans ensuring milestones are delivered on time and within budget.
• Coordinate communication between scientific teams, regulatory affairs, and external stakeholders and translate discussions into actions and plans.
• Identify technical, regulatory, operational, and logistical risks; define mitigations and elevate significant issues.
• Support Head of Program Management in establishing and maintaining a robust PM culture.

Kenntnisse

Project management

Cross-functional coordination

Risk management

Analytical reasoning

English fluency

German language

Ausbildung

MSc in chemistry/pharma/analytics

PhD in related discipline

Jobbeschreibung

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 elevate 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 Schärli
Senior Talent Acquisition Manager
mail:[e-mail]