QA Specialist - GMP, CAPA & Process Improvement

Fertin Pharma A/S; Vejle; On-site; DKK 650,000 - 850,000; Full time

Job summary

Fertin Pharma A/S in Denmark is seeking a QA Specialist to work close to pharmaceutical operations, ensuring product quality and strengthening manufacturing processes. You will combine day-to-day quality activities with investigations, problem solving, and continuous improvement.

You will collaborate across Quality and Operations, participate in deviation investigations, release of products, reviews of manufacturing docs, and support inspections.

Qualifications

• Educational background is flexible if the candidate understands processes and turns quality issues into practical solutions.
• Experience in pharmaceutical or highly regulated industries is preferred.
• Possession of qualifications for QP Delegate under Danish requirements is advantageous.
• Familiarity with GMP and pharmaceutical QMS is beneficial.

Responsibilities

• Support and approve deviation investigations, including root-cause analysis and CAPAs.
• Provide quality support to manufacturing and participate in release of products.
• Review and approve manufacturing documentation and participate in change controls.
• Contribute to risk assessments and ongoing quality improvement activities.
• Support inspection and audit readiness and cross-functional quality projects.

Skills

Deviation investigations

Root-cause analysis

CAPA

Quality management

GMP

Job description

Fertin Pharma A/S in Denmark is seeking a QA Specialist to work close to pharmaceutical operations, ensuring product quality and strengthening manufacturing processes. You will combine day-to-day quality activities with investigations, problem solving, and continuous improvement.

You will collaborate across Quality and Operations, participate in deviation investigations, release of products, reviews of manufacturing docs, and support inspections.