QA Specialistas(-ė)

About the role

Profarma, a European pharmaceutical laboratory with MIA licence and GMP certification, is looking for a QA Specialist to join its quality team in Lithuania. The role focuses on ensuring that all quality processes comply with GMP standards and are executed on schedule.

Key responsibilities

• Prepare, review and administer GMP documentation.
• Manage deviations, CAPA, change controls and risk assessments.
• Support audit and inspection readiness.
• Oversee qualification documentation for suppliers and contract partners.
• Administer trainings, procedures and other QMS processes.
• Collaborate with QC, clients and internal departments.
• Help guarantee that quality activities are performed timely and according to GMP requirements.

Required profile

• Experience working in a QA/GMP environment within a pharmaceutical company.
• Solid understanding of basic GMP and quality‑system principles.
• Ability to organise work independently and meet deadlines.
• Meticulous, responsible and capable of prioritising tasks.
• Clear communication and teamwork skills.
• Fluent in Lithuanian and English.

Required skills

• GMP
• CAPA
• QMS
• Risk assessment

What we offer

• Work in a professional pharmaceutical quality team.
• Extensive practical GMP experience.
• Varied interaction with QC labs, clients, auditors and regulatory authorities.
• Salary commensurate with experience and competencies.