Job Opportunity: Cleaning Validation Consultant

About the Role

Are you ready to play a pivotal role in shaping the future of the Life Science industry? GMP Konsulenterne is looking for a skilled Validation Consultant to join our team and contribute to exciting and varied projects in the Danish pharmaceutical industry. This is an exceptional opportunity to apply your expertise while working with some of Denmark’s most influential companies.

Key Responsibilities

Conducting validation studies to document cleaning process efficiency.
Collaborating with clients to establish procedures ensuring the removal of product residues and contaminants.
Preparing validation protocols and reports documenting the entire validation process and results.
Reviewing validation activities and documents to ensure compliance with regulatory requirements.

Qualifications and Experience

At least 3 years of experience in the life science industry.
Strong technical knowledge and ability to navigate cross-functional collaborations.
Experience within CIP and Wash.
Excellent communication skills in both Danish and English.
Valid driver’s license.

Personal Skills

Curious, proactive, and outgoing.
Ambitious, passionate, and solution-oriented.
Structured, creative, and empathetic.
A team player with a collaborative mindset.

Educational Background

Degree in Pharmacy, Engineering, or a related field, with documented competencies in validation.

Details

Hours: 37 hours per week.
Location: Kalundborg.
Start Date: Between February 1, 2025, and April 1, 2025.

About Us

GMP Konsulenterne is a leading consultancy firm serving the pharmaceutical industry. Our team of +50 professionals works closely with public and private organizations to deliver quality and compliance in their operations and development processes.

How to Apply

If this exciting opportunity matches your profile, please send your CV and a motivated application to: career@gmp-cgroup.com or call Mai-Britt Olafsson at +45 5353 4378. We look forward to hearing from you!