Project Manager for Compliance and Process Improvement Projects
Novo Nordisk
.Do you have project management experience in a pharmaceutical setting or with implementing requirements for materials or products? Are you goal-oriented, eager to enhance your project execution skills, and driven to lead initiatives that scale our global supply chain and material portfolio for the future?
If you’re passionate about transforming quality requirements into practical solutions that meet the needs of patients and operational workflows, we invite you to join Material Manufacturing Development (Mat. ManDev) – RAW.
Take the next step in your career and apply today!The position
As Project Manager, your primary role entails owning and managing projects from inception to execution. You will focus on:
You can anticipate being involved in projects related to GMP, quality improvements, authority requirements but also improvements needed for scaling up our organization.
Some of your key tasks include:
You will work closely with GMP material scientists and other project managers supporting the department, but your activities will also include communicating across all levels and business areas in the organization.Qualifications
To be considered for this role, we imagine you:
You are proactive, independent, and excel in communication and collaboration. With a structured, analytical mindset, you prioritize effectively, make sound decisions, and ensure timely follow-ups. You value diverse opinions while guiding team decisions and think strategically, adapting to changes that impact projects.About the department
You will join Material ManDev – RAW, in Product Supply, Sourcing Operations. The position is in the Processes & Raw Material Specifications team, but you will support the entire department. In the team we are today a mix of material scientists and project managers.
The department consist of approximately 60 employees, located in Bagsværd, but moving to Taastrup in the beginning of 2026.
In the RAW Department, we manage the implementation of complex materials (e.g., raw materials, excipients) from development to production and maintain documentation for existing materials. We work closely with functions such as CMC, QC, QA, supply, warehouses, production sites, and external suppliers and CMOs.
You’ll join a team of talented individuals with diverse perspectives, where we prioritize strong relationships and an inclusive environment that values the diversity of our employees.
Bagsværd, Hovedstaden
Tue, 24 Dec 2024 23:19:47 GMT
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