Pharma QA Specialist - GMP/GDP, 3PL Audits & Compliance

Alloga; Veghel; On-site; EUR 55,000 - 70,000; Full time

Job summary

Alloga (Nederland) B.V. is seeking a QA Specialist to support the Quality Management System within a pharmaceutical 3PL environment. You will ensure activities comply with GDP/GMP standards, internal procedures, and customer requirements while driving continuous improvement.

The role focuses on audits, CAPA, documentation, and training to promote quality awareness across the organization. A Bachelor’s degree in a related field and at least 2 years of QA experience are preferred.

Qualifications

• Bachelor's degree or equivalent in pharmacy, life sciences, quality, or related field.
• Minimum 2 years’ QA experience in pharma, healthcare, logistics or 3PL.
• Knowledge of GDP, GMP and pharma quality standards.
• Experience with audits, deviations, CAPA, document control and QMS.

Responsibilities

• Prepare, perform, and report internal audits of systems and processes.
• Coordinate external audits by customers, suppliers, certification bodies, and regulators.
• Conduct supplier audits and follow up on findings.
• Monitor non-conformances, complaints, CAPAs and improvement actions.
• Identify quality risks and implement corrective and preventive measures.
• Maintain and improve quality procedures, work instructions and quality manual.
• Support document control and management of quality records and data in relevant systems.
• Provide quality-related advice to operations and support process improvements.
• Develop or deliver training materials to promote quality awareness and compliance.
• Communicate quality, safety and regulatory requirements organization-wide.
• Represent QA in interactions with customers, suppliers, auditors and regulators.

Skills

QA

Audits

CAPA

Document control

Quality systems

Training

Analytical

Communication

Education

Bachelor's degree in pharmacy or life sciences

Job description

Alloga (Nederland) B.V. is seeking a QA Specialist to support the Quality Management System within a pharmaceutical 3PL environment. You will ensure activities comply with GDP/GMP standards, internal procedures, and customer requirements while driving continuous improvement.

The role focuses on audits, CAPA, documentation, and training to promote quality awareness across the organization. A Bachelor’s degree in a related field and at least 2 years of QA experience are preferred.