QA Specialist: GMP Compliance & Validation

Tecnimede Group; Sintra; On-site; EUR 32,000 - 42,000; Full time

Job summary

Tecnimede Group in Sintra is seeking a Quality Assurance Specialist to strengthen our lifecycle of pharmaceutical products. You will implement and maintain Quality Management Systems, ensure compliance with GMP, and drive continuous improvement across manufacturing and quality control processes.

The ideal candidate holds a Degree in Pharmaceutical Sciences, has experience in the pharmaceutical industry, and is fluent in English.

Qualifications

• Degree in Pharmaceutical Sciences.
• Professional experience in the Pharmaceutical Industry.
• Experience in Quality Management Systems certification processes.
• Knowledge of national and European regulations applicable to the sector.
• Experience in Validation of Manufacturing Processes (preferred).
• Experience in Cleaning Validation (preferred).
• Experience in using Document Management Systems.
• Mastery of the English language.

Responsibilities

• Implement and maintain Quality Management Systems in accordance with legislation and company procedures.
• Support development and review of procedures, validations/qualifications, and corrective actions.
• Collaborate with cross‑functional teams to ensure GMP compliance and continuous improvement.

Skills

Quality Management Systems

Good Documentation Practices

English language

Regulatory knowledge

Validation

Education

Degree in Pharmaceutical Sciences

Tools

Document Management Systems

Job description

Tecnimede Group in Sintra is seeking a Quality Assurance Specialist to strengthen our lifecycle of pharmaceutical products. You will implement and maintain Quality Management Systems, ensure compliance with GMP, and drive continuous improvement across manufacturing and quality control processes.

The ideal candidate holds a Degree in Pharmaceutical Sciences, has experience in the pharmaceutical industry, and is fluent in English.