Validation Team Lead (Copenhagen HQ) at Eupry ApS
København, , Denmark -
Full Time


Start Date

Immediate

Expiry Date

26 Sep, 25

Salary

0.0

Posted On

27 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

English, Life Science Industry, Medical Devices, Project Management Skills, Life Sciences, Danish, Pharmaceuticals

Industry

Information Technology/IT

Description

We are seeking a driven and experienced Validation Team Lead to lead our growing team of validation engineers and deliver top-tier CQV (Commissioning, Qualification, and Validation) projects to clients across highly regulated industries such as within pharmaceutical manufacturing and distribution. Based at our headquarters in Copenhagen, this is a unique opportunity to take ownership in a high-impact leadership role within a fast-scaling, innovation-driven company.

YOUR EXPERIENCE & EDUCATION

  • Bachelor’s or Master’s degree in engineering, life sciences, or another technical discipline
  • Leadership background with experience managing or mentoring technical teams
  • Proven experience in CQV, with a focus on regulated industries such as pharmaceuticals, biotech, or medical devices
  • Familiarity with temperature mapping, validation protocols, GxP documentation, and international regulatory expectations
  • Hands-on project management skills and the ability to lead customer-facing projects independently
  • Comfortable working in scale-up or agile environments
  • Fluent in English (spoken and written); Danish is a plus but not required
  • Willingness to travel on business trips—primarily domestic, and within the EU
Responsibilities
  • Lead and manage a team of 6 validation engineers delivering CQV services to a wide range of clients, including top pharmaceutical companies
  • Drive project execution of CQV activities involving particularly temperature mapping of warehouses and Temperature Controlled Units (TCUs)
  • Plan, coordinate, and prioritize daily project activities to ensure timely, high-quality delivery
  • Provide technical leadership, mentorship, and support to your team on CQV best practices and regulatory expectations
  • Develop and review qualification protocols (IQ/OQ/PQ) and related documentation in alignment with GMP, GxP, and client-specific requirements
  • Execute temperature mapping and qualification activities on-site and remotely as needed
  • Serve as a technical consultant and primary point of contact for clients throughout CQV projects, ensuring clarity, transparency, and satisfaction
  • Collaborate with internal cross-functional teams including R&D, QA, and Customer Success to support smooth delivery of services
  • Maintain and improve internal validation procedures and knowledge base to support scalability
  • Align with the Global Validation Manager to implement and maintain global validation standards and practices
Loading...