Quality Clinical Consultant

We are looking for a Quality Clinical Consultant to support the Quality System and participate in the start-up and conduct of clinical trials. The selected candidate will be responsible for document review, management of non-conformances, and coordination of clinical supplies, becoming a key member of the clinical operations team.

Requirements

• Bachelor or Master degree in biological or (para-) medical sciences, Life Science, Quality Assurance, Clinical or equivalent by experience
• Minimum 2 years of experience in a Quality role within the medical device, or pharmaceutical industry.
• Proven experience with implementing and maintaining a QMS compliant with GCP.
• Deep knowledge of GxP (mainly GCP), ISO 9001, ISO 13485 and applicable regulatory requirements applicable with the IVD, MD, Pharma and LifeScience industries.
• Strong understanding of risk-based thinking and quality system integration
• Experience in QMS software systems and document control tools.
• Excellent oral and written communications skills
• Excellent interpersonal skills, inspirational and motivational skills
• Analytical and problem-solving skills.
• Attention to detail and organizational skills.
• Demonstrates integrity and ethical conduct.
• Proactive and results-oriented mindset.
• Demonstrates ability to make timely and well-reasoned decisions
• Ability to maintain composure in difficult circumstances and sensitive to cultural differences
• Fluent in English and Spanish. Other languages are a plus

Benefits

• A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.