GMP QA Scientist — Flexible Hours, Hybrid Work

Kymos Group; Cerdanyola del Vallés; Hybrid; EUR 36,000 - 48,000; Full time

Benefits offered by this job

Hybrid work model

Canteen on site

Rooftop terrace

Job summary

Remoteo is seeking a Quality Assurance Scientist for our GMP Quality Assurance Department in Spain. The role focuses on reviewing documentation, auditing analytical records, and supporting self-inspections and regulatory inspections in a hybrid work setting.

The candidate should have a degree in chemistry, pharmacy, biosciences or related field with at least 1 year in QA/QC/manufacturing in the pharmaceutical industry; fluency in English and Spanish is required.

Qualifications

• Degree in chemistry, pharmacy, biosciences or related.
• 1 year of experience in Quality Assurance or Quality Control or Manufacturing in the pharmaceutical industry.
• Knowledge of Pharmaceutical Analysis, QC and QA following cGMP requirements.
• High level of English and Spanish (written and spoken).

Responsibilities

• Review and approve documentation involved in analytical activity (CoA, protocols, reports, SOPs, product specifications).
• Audit analytical documentation to ensure compliance with internal and external standards (cGMP).
• Participate in the QA Annual Program of self-inspections.
• Verify conformity of quality controls in company processes.
• Participate in evaluation of deviations, OOS/OOT, complaints, CAPA and Change Controls.
• Review Quality/Technical Agreements with subcontractors, especially batch certification activities.
• Collaborate in audits by clients or subcontracted manufacturers and support regulatory inspections.
• Contribute to implementation and improvement of the company and subcontractors' quality.

Skills

English fluency

Spanish fluency

Education

Degree in chemistry/pharmacy/biosciences or related

Job description

Remoteo is seeking a Quality Assurance Scientist for our GMP Quality Assurance Department in Spain. The role focuses on reviewing documentation, auditing analytical records, and supporting self-inspections and regulatory inspections in a hybrid work setting.

The candidate should have a degree in chemistry, pharmacy, biosciences or related field with at least 1 year in QA/QC/manufacturing in the pharmaceutical industry; fluency in English and Spanish is required.