Analytical Scientist – GMP & Regulatory Excellence

Novo Nordisk A/S; Denmark; Remote; DKK 570,000 - 838,000; Full time

Job summary

Novo Nordisk A/S is seeking an Analytical Scientist to provide GMP expertise to CMOs and lead analytical programs across the lifecycle. The role includes supporting regulatory submissions and collaborating with international partners.

You will join External Analysis & QC, a department overseeing analytical strategies in collaboration with US and Danish teams, with potential travel of up to 14 days per year.

Qualifications

• Master’s degree in a relevant scientific discipline.
• Minimum 3 years of experience in pharma or similar.
• Hands-on GMP environment experience (e.g., QC lab).
• Strong knowledge of GMP, ICH guidelines, and regulatory requirements.
• Experience with deviations, change requests, and out-of-specifications.
• Professional proficiency in English (spoken and written).

Responsibilities

• Provide scientific and GMP expertise to CMOs and stakeholders.
• Support analytical activities from late-stage clinical studies through lifecycle.
• Lead tech transfer and analytical method implementation with partners.
• Author/edit SOPs, review protocols, reports, tech transfer plans, and docs.
• Build and optimize processes and SOPs for daily work.

Skills

GMP knowledge

ICH guidelines

English proficiency

SOP development/editing

Tech transfer

Education

Master's degree in Pharmacy, Chemistry, Biochemistry, Chemical Engineering or related field

Job description

Novo Nordisk A/S is seeking an Analytical Scientist to provide GMP expertise to CMOs and lead analytical programs across the lifecycle. The role includes supporting regulatory submissions and collaborating with international partners.

You will join External Analysis & QC, a department overseeing analytical strategies in collaboration with US and Danish teams, with potential travel of up to 14 days per year.