API Lead

GE HealthCare; Oslo fylke; Hybrid; GBP 120,000 - 180,000; Full time

Job summary

GE HealthCare is seeking an API Lead to provide technical leadership for API development and manufacturing through CMOs, covering early development to scale-up and regulatory CMC decisions.

Ideal candidate will lead cross-functional teams and ensure quality, timelines, risks, costs, and deliverables align across partners across GMP and regulatory contexts.

Qualifications

• PhD or MSc in Organic Chemistry, Pharmaceutical Chemistry, Chemical Engineering, or a related scientific or engineering discipline.
• Experience in API development, scale-up, technology transfer, or manufacturing.
• Experience managing CMOs or outsourced pharmaceutical development and manufacturing activities.
• Strong GMP requirements, pharmaceutical development, and regulatory CMC knowledge.
• Strong API characterization, analytical method development, impurity investigations, and impurity-control strategies.
• Experience preparing or supporting CMC documentation for regulatory submissions.
• Excellent written and verbal communication and stakeholder-management skills.
• Fluent in English, both written and verbal.

Responsibilities

• Lead the development and manufacturing of APIs, precursors, and key materials at external CMOs from early development through commercialization.
• Act as the primary technical interface between internal project teams, CMOs, key suppliers, and other external development and manufacturing partners.
• Define development strategies, deliverables, timelines, risks, and priorities, and oversee process development, optimization, scale-up, technology transfer, and GMP manufacturing.
• Contribute to assessing selecting, qualifying, and onboarding CMOs and key suppliers based on technical capabilities, capacity, quality, cost, timelines, and risk, and monitor ongoing performance.
• Lead technical, quality, and manufacturing challenges, including deviations, investigations, change controls, and impurity-related issues.
• Define API starting material, characterization, and impurity-control strategies, including regulatory justification in line with applicable ICH guidelines.
• Prepare and review CMC documentation for manufacturing activities, and regulatory submissions.
• Collaborate across Quality, Regulatory, Analytical Development, Manufacturing, Supply Chain, Sourcing, IP, Legal, and project teams to ensure compliant execution in line with applicable GMP, regulatory, quality, and EHS requirements.

Skills

Project leadership

Stakeholder management

Scientific writing

Regulatory coordination

English fluency

Education

PhD or MSc in Organic/Chemical/Pharmaceutical Chemistry or Chemical Engineering

Job description

Job Description Summary

As API Lead, you provide technical leadership for the development and manufacturing of precursors and active pharmaceutical ingredients (APIs) through external Contract Manufacturing Organizations (CMOs). You lead activities from early development and process optimization through scale-up, technology transfer, GMP manufacturing, to late-stage development As the primary technical interface between internal project teams and external partners, you ensure that quality, timelines, risks, costs, and technical deliverables remain aligned. You apply your expertise in synthetic chemistry, GMP, and regulatory CMC requirements to guide technical decisions and resolve complex development and manufacturing challenges. Through strong stakeholder management, you bring internal and external experts together to deliver robust and compliant API manufacturing solutions.

Ideally this role is based in Oslo, where the team is based. However, we offer flexibility, and the role can also be based at our sites in the Netherlands (Eindhoven), or UK (Pollard Wood).

Job Description

GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

GE HealthCare Pharmaceutical Diagnostics (PDx) is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world.

Essential Responsibilities

• Lead the development and manufacturing of APIs, precursors, and key materials at external CMOs from early development through commercialization.

• Act as the primary technical interface between internal project teams, CMOs, key suppliers, and other external development and manufacturing partners.

• Define development strategies, deliverables, timelines, risks, and priorities, and oversee process development, optimization, scale-up, technology transfer, and GMP manufacturing.

• Contribute to assessing selecting, qualifying, and onboarding CMOs and key suppliers based on technical capabilities, capacity, quality, cost, timelines, and risk, and monitor ongoing performance.

• Lead technical, quality, and manufacturing challenges, including deviations, investigations, change controls, and impurity-related issues.

• Define API starting material, characterization, and impurity-control strategies, including regulatory justification in line with applicable ICH guidelines.

• Prepare and review CMC documentation for manufacturing activities, and regulatory submissions.

• Collaborate across Quality, Regulatory, Analytical Development, Manufacturing, Supply Chain, Sourcing, IP, Legal, and project teams to ensure compliant execution in line with applicable GMP, regulatory, quality, and EHS requirements.

Basic Qualifications and Requirements

• PhD or MSc in Organic Chemistry, Pharmaceutical Chemistry, Chemical Engineering, or a related scientific or engineering discipline.

• Relevant experience in API, precursor, or pharmaceutical process development, including process development, scale-up, technology transfer, or manufacturing.

• Demonstrated experience managing CMOs or outsourced pharmaceutical development and manufacturing activities.

• Strong knowledge of GMP requirements, pharmaceutical development, and regulatory CMC expectations.

• Strong technical understanding of API characterization, analytical method development, impurity investigations, and impurity-control strategies.

• Experience preparing or supporting CMC documentation for regulatory submissions and health-authority interactions.

• Excellent written and verbal communication and stakeholder-management skills, with the ability to influence decisions and manage competing priorities in cross-functional and multicultural environments.

• Fluent in English, both written and verbal.

Behaviors

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Total Rewards

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

Inclusion & Diversity

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or age, disability, protected veteran status or other characteristics protected by law.

#Onsite

#LI-WRO

Additional Information

Relocation Assistance Provided: No