GMP QA Scientist - Pharma (Hybrid, Flexible Hours)

Kymos Group; Barcelona; Hybrid; EUR 45,000 - 55,000; Full time

Benefits offered by this job

Hybrid work

Flexible hours

23 vacation days per year + holidays

Canteen & rooftop space

Office in Barcelona area

Job summary

Kymos Group is hiring a Quality Assurance Scientist for our GMP area within the QA Department in Barcelona. You will review and approve CoA, protocols, reports, and SOPs, and ensure cGMP compliance across analytical activities.

The role requires a degree in chemistry, pharmacy, biosciences or related with at least 1 year in QA/QC/manufacturing in pharma, and a high level of English and Spanish. Hybrid work, mainly in the office, with a dynamic team and growth opportunities.

Qualifications

• Degree in chemistry, pharmacy, biosciences or related.
• 1 year of experience in QA/QC/manufacturing in the pharmaceutical industry.
• Knowledge of GMP/cGMP requirements and pharmaceutical analysis.
• High level of English and Spanish written and spoken.

Responsibilities

• Review and approve documentation: CoA, protocols, reports, SOPs, product specifications.
• Audit analytical documentation to ensure cGMP compliance.
• Participate in the QA Annual Program of self-inspections.
• Verify conformity of quality controls in company processes.
• Evaluate deviations, OOS/OOT, complaints, CAPA and Change Controls.
• Review Quality/Technical Agreements with subcontractors for batch certification.
• Collaborate in client or subcontractor audits and support regulatory inspections.
• Participate in QA improvement initiatives across the company and subcontractors.

Skills

Quality Assurance

Quality Control

Pharmaceutical Analysis

English Proficiency

Spanish Proficiency

Education

Degree in chemistry, pharmacy, biosciences or related

Job description

Kymos Group is hiring a Quality Assurance Scientist for our GMP area within the QA Department in Barcelona. You will review and approve CoA, protocols, reports, and SOPs, and ensure cGMP compliance across analytical activities.

The role requires a degree in chemistry, pharmacy, biosciences or related with at least 1 year in QA/QC/manufacturing in pharma, and a high level of English and Spanish. Hybrid work, mainly in the office, with a dynamic team and growth opportunities.