QA Consultant — Life Sciences, GMP & Compliance

QbD Group | Spain; Barcelona; On-site; EUR 42,000 - 60,000; Full time

Job summary

QbD Group is seeking a Quality Assurance Consultant to support GMP activities across pharma, biotech, medical devices, and digital health. You will join a fast-growing, international team of 650+ experts, gaining hands-on experience in GMP batch review, deviation handling, and regulatory compliance.

The role offers exposure to audits, multiple client projects, and a path to grow as a quality professional within a stable employer. Fluency in Spanish and English is required.

Qualifications

• 1–7 years of GMP experience required.
• Master’s degree in Pharmaceutical Sciences or related field.
• Fluent in Spanish and English.

Responsibilities

• Gain hands-on GMP experience: support batch review, release, and learn GMP documentation.
• Expand quality systems knowledge: work on deviations, CAPAs, and change controls.
• Experience diverse environments across pharma/biotech/MedTech projects.
• Develop stakeholder communication and problem-solving skills.
• Assist with audits and inspections: prepare documentation and interact with authorities.

Skills

GMP experience

Quality assurance

Stakeholder communication

Problem solving

Education

Master’s in Pharmaceutical Sciences

Job description

QbD Group is seeking a Quality Assurance Consultant to support GMP activities across pharma, biotech, medical devices, and digital health. You will join a fast-growing, international team of 650+ experts, gaining hands-on experience in GMP batch review, deviation handling, and regulatory compliance.

The role offers exposure to audits, multiple client projects, and a path to grow as a quality professional within a stable employer. Fluency in Spanish and English is required.