Pharma QA Analyst – GMP Compliance & Documentation

jcyl.es - jobboard; Agder; On-site; NOK 550,000 - 750,000; Full time

Job summary

jcyl.es - jobboard is seeking a QA professional for pharmaceutical settings in Norway, Agder. The role requires a Bachelor's degree in a scientific field and 1–3 years in QA.

Applicants should have strong GMP/GDP knowledge, regulatory familiarity (FDA/EMA/WHO), and excellent attention to documentation and communication. Independent work and teamwork are valued as part of a collaborative environment.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology, or related scientific field.
• 1–3 years’ experience in a pharmaceutical QA environment (preferred).
• Strong understanding of GMP, GDP, and regulatory guidelines (FDA, EMA, WHO).
• Excellent attention to detail and documentation skills.
• Strong analytical, problem-solving, and communication abilities.
• Ability to work independently and as part of a team.

Skills

GMP/GDP knowledge

Regulatory guidelines

Analytical skills

Problem solving

Communication skills

Documentation skills

Independent work

Teamwork

Education

Bachelor’s degree in Pharmacy, Chemistry, Biology, or related scientific field

Job description

jcyl.es - jobboard is seeking a QA professional for pharmaceutical settings in Norway, Agder. The role requires a Bachelor's degree in a scientific field and 1–3 years in QA.

Applicants should have strong GMP/GDP knowledge, regulatory familiarity (FDA/EMA/WHO), and excellent attention to documentation and communication. Independent work and teamwork are valued as part of a collaborative environment.