Plan, coordinate, and support sampling activities, including execution, documentation, and alignment with project and routine laboratory needs.
Review, evaluate, and approve analytical test results for release, stability, and project-related activities in accordance with applicable procedures.
Prepare, review, and approve analytical protocols, reports, trend analyses, KPIs/KQIs, and registration-related documentation.
Lead or contribute to analytical project activities, including method implementation, analytical transfers, new product introduction, and routine laboratory readiness.
Serve as Single Point of Contact or Subject Matter Expert for assigned products, pipeline activities, external initiatives, audits, inspections, and technical assessments.
Manage deviations, OOx investigations, CAPA definition, analytical weak points, and continuous improvement actions to ensure robust laboratory performance.
Contribute to supplier qualification, service provider management, contracts, SLAs, SOWs, QAAs, budgeting activities, and cross-functional governance meetings.
Ensure all activities comply with cGxP, data integrity, Quality, and HSE requirements, including equipment maintenance, calibration planning, training, risk identification, and safe working practices.
Responsibilities
Plan, coordinate, and support sampling activities
Review, evaluate, and approve analytical test results
Prepare, review, and approve analytical protocols and reports
Lead or contribute to analytical project activities
Serve as Single Point of Contact or Subject Matter Expert
Manage deviations, investigations, and continuous improvement actions
Contribute to supplier qualification and service provider management
Ensure compliance with cGxP, data integrity, Quality, and HSE requirements
Requirements
Technical education with 3–5 years of relevant experience, or a university degree in Pharmacy, Chemistry, or a related scientific discipline with 0–4 years of relevant experience
Experience in the pharmaceutical industry or analytical laboratories within a GMP-regulated environment
Strong knowledge of Quality Control testing and GxP standards
Experience supporting analytical release and stability testing
Ability to collaborate effectively across functions and teams
Strong communication skills in English and local language
Proficiency in MS Office and standard IT systems
Tech stack
MS Office
Benefits
Competitive benefits in kind
Flexible and hybrid working options
Minimum of 14 weeks paid parental leave
Performance-based bonus eligibility
Company
Novartis
Pharmaceuticals
At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.
