Senior Consultant (Validation)

Devote Consulting; København; On-site; DKK 600,000 - 850,000; Full time

Job summary

Devote Consulting is seeking a Senior Consultant to join our team as a GxP validation expert. You’ll validate systems, data, and processes in the pharmaceutical life sciences sector, supporting R&D and clinical operations.

The role emphasizes stakeholder management, agile delivery, and the ability to drive compliant documentation. You’ll work with clients and fellow consultants to deliver high-impact validation projects and improvements.

Qualifications

• Master’s degree in a relevant field or higher.
• 5+ years as Validation Lead for GxP systems in regulated industries (Pharma/Biotech/MedTech).
• Excellent verbal and written English communication skills.
• Experience with agile delivery methods is an advantage.

Responsibilities

• Deliver impactful changes in processes, data, and systems for life science projects (R&D and clinical operations).
• Redesign validation and quality processes to improve efficiency.
• Lead project planning and ensure delivery of compliance documentation with stakeholders.

Skills

English language proficiency

Analytical thinking

Stakeholder management

Agile delivery

Education

Master's degree in business administration, IT, life sciences, or related field

Tools

CTMS

eTMF

RBM

EDC

Job description

Join Our Team at Devote Consulting

SENIOR CONSULTANT - VALIDATION

Are you an experienced professional in GxP system validation? Devote Consulting is expanding, and we’re looking for a Senior Consultant to join our team. If you have deep expertise in validating GxP system applications, platforms, and data in the pharmaceutical industry, we want to hear from you!

Are We Looking for You?

• You thrive in the fast-paced life of a consultant and enjoy learning, sharing, and collaborating with others
• You take ownership of your tasks, always delivering high-quality results
• You are driven by the desire to make a difference for patients by improving business processes and creating essential compliance documentation
• You have experience with agile delivery methods and understand how to optimize business processes using data efficiently
• You’ll excel in a high-achieving culture that fosters both personal and professional growth

What You’ll Do

• Supporting projects: Deliver impactful changes in processes, data, and systems for the life science industry, focusing on R&D and clinical operations
• Business process optimization: Redesign validation and quality processes to enhance efficiency
• Stakeholder management: Lead project planning and ensure the delivery of compliance documentation for processes and systems in collaboration with other consultants and client representatives
• Driving project progress: Oversee quality and ensure timely delivery of project deliverables

Your Qualifications

• A master’s degree in business administration, IT, life sciences, or a related field
• 5 years of experience as a Validation Lead for GxP systems within regulated industries such as Pharma, Biotech, or MedTech
• Excellent verbal and written communication skills in English
• A strong analytical and problem-solving mindset, with a passion for making an impact
• Experience with agile delivery methods is an advantage
• Using Clinical R&D systems (CTMS, eTMF, RBM, EDC, etc.) or medical devices is an advantage
• Certifications in Life Science R&D platforms are an advantage

What We Offer

At Devote Consulting, we offer a position where you can take ownership, influence key outcomes, and make a meaningful impact in your everyday work. You’ll have the opportunity to lead multiple projects as a specialist, project manager or Validation Lead in a dynamic and growing team.

Ready to Join Us?

We welcome individuals from all backgrounds and are committed to a recruitment process that ensures equal opportunities for all applicants. We review applications on a rolling basis, so