Analytical Project Leader / Scientist / Senior Scientist – Basel

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Wir suchen eine:n Senior Associate Scientist / Analytical Development (m/w/d) – Basel
Analytical Project Leader / Scientist / Senior Scientist (m/w/d) – Basel
We are currently looking for an experienced Analytical Project Leader / Scientist / Senior Scientist for a temporary assignment in Basel within Analytical Development & Quality Control.
The Analytical Research & Development department is part of Synthetic Molecules Technical Development and is globally responsible for advancing analytical methodologies, performing in-depth analyses of active pharmaceutical ingredients and dosage forms, and preparing regulatory documentation for submissions to health authorities.
In this role, you will lead analytical development activities for small molecule projects, from early development stages through to commercialization. You will work closely with internal laboratories, cross-functional stakeholders and external partners such as CLOs/CDMOs.
General Conditions
Start date: asap
Latest possible start date: 1 August 2026
Duration: 12 months
Extension: rather unlikely
Workload: 100%
Location: Basel
Home office: possible, up to 2 days per week after onboarding
Travel: no
Working hours: standard working hours
GMP environment: yes
Criminal record extract: not required
Main Responsibilities
Develop a phase-appropriate control strategy for drug substances and drug products
Coordinate analytical activities within assigned small molecule development projects
Generate physical and chemical data for materials, drug substances and drug products
Develop, improve and validate analytical test methods and other analytical controls
Ensure complete, high-quality and timely documentation of analytical activities and results
Plan and document experiments and results independently
Prepare analytical documentation for regulatory submissions such as IND and NDA
Supervise internal laboratory activities and/or testing activities at CLOs/CDMOs
Collaborate effectively with stakeholders across different departments
Coach technicians and junior scientists on project-related activities
Act as a central point of contact for analytical project information
Ensure all work is conducted in compliance with cGMP, safety standards and regulatory requirements
Must Haves
Master’s degree or Ph.D. in chemistry, pharmacy or a related field
At least 3 years of professional experience in analytical development of drug substances or drug products for small molecules
Strong knowledge of chemistry, including synthesis, purification and characterization
Expertise in key analytical techniques, especially HPLC and UPLC
Proven experience in developing and validating ICH-compliant analytical methods
Experience with degradation and stability studies for small molecules, including forced degradation and impurity profiling
Understanding of key requirements for drug substance and drug product specifications
Excellent command of English
Strong quality mindset and excellent attention to detail
Ability to coordinate analytical work across internal and external stakeholders
Open-minded, goal-oriented and comfortable working in a fast-developing environment
Strong collaboration skills, also in stressful project situations
Nice to Haves
German language skills
Familiarity with statistical analysis of analytical data
Digital savviness and interest in supporting digital transformation initiatives
Experience working with external laboratories, CLOs or CDMOs
Ideal Candidate Profile
The ideal candidate is an experienced analytical chemist with a strong background in small molecule drug development. They should bring hands-on expertise in HPLC/UPLC, ICH-compliant analytical method development and validation, stability studies, forced degradation and impurity profiling.
This role is not only focused on laboratory execution. The ideal person should also be able to coordinate analytical project activities, manage internal and external stakeholders, supervise laboratory or external testing activities, ensure high-quality documentation and contribute to regulatory submissions. A strong cGMP mindset, attention to detail and the ability to work independently in a dynamic project environment are essential. jid5e52145a jit0519a jiy26a