Analytical Scientist (Drug Products)

Proclinical Consulting; Basel; On-site; CHF 110,000 - 140,000; Full time

Job summary

Proclinical Consulting in Basel seeks an Analytical Scientist to join the Analytical Research and Development (ARD) team within Technical R&D. You will characterise and analyse drug substances and products, with a focus on Radio Ligand Therapy (RLT).

The role is integral to development and manufacturing of innovative medicines and requires right to work in Switzerland or EU passport. You will develop and validate UHPLC, LC-MS and UV-Vis methods, maintain instruments, and ensure compliance with

Qualifications

• Degree in Life Sciences or equivalent.
• Proficiency with UHPLC, LC-MS and UV-Vis analytical methods.
• Experience characterising peptides and their analytics.

Responsibilities

• Develop and implement analytical methods for characterising and quantifying RLT substances and products.
• Plan, execute, document, interpret, and report experiments with quality and timelines.
• Contribute to RLT analytical toolbox using LC-MS and related techniques.
• Present findings in cross-functional groups and meetings.
• Troubleshoot analytical methods and instrumentation issues with scientific rigor.
• Support lean, efficient laboratory practices and instrument maintenance.
• Ensure proper documentation and adherence to lab practices.

Skills

UHPLC

LC-MS

UV-Vis

Peptides analysis

ICH regulations

International teams

English fluency

Education

Degree in Life Sciences

Tools

Chromatography software

Job description

Are you an analytical scientist looking to play a key role in developing innovative radioligand therapies that could transform patient care? Proclinical is seeking an Analytical Scientist to join the Analytical Research and Development (ARD) team within the Technical R&D department. In this role, you will play a key part in the characterization and analysis of drug substances and drug products, with a focus on Radio Ligand Therapy (RLT). This position is integral to the development and manufacturing of innovative medicines. Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities

• Develop and implement analytical methods for characterizing and quantifying RLT drug substances and drug products.
• Plan, execute, document, interpret, and report scientific experiments, including analytical method development and testing, ensuring adherence to quality standards and timelines.
• Contribute to the development of an RLT analytical toolbox using advanced techniques such as Liquid Chromatography-Mass Spectrometry (LC-MS).
• Participate in scientific exchange groups and present findings.
• Troubleshoot analytical methods and instrumentation issues, providing scientific solutions.
• Implement lean, efficient, and environmentally sustainable practices in the laboratory.
• Maintain laboratory instruments and ensure smooth day-to-day operations.
• Ensure proper documentation and adherence to laboratory practices during all activities.

Key Skills And Requirements

• Degree in Life Sciences sector or equivalent.
• Proficiency in analytical methods and separation techniques such as UHPLC, LC-MS, and UV-Vis.
• Strong knowledge of peptides and their analytical characterization.
• Innovative mindset with the ability to develop novel approaches to complex scientific challenges.
• Familiarity with analytical software, such as chromatography tools.
• Understanding of ICH guidelines and regulatory requirements for analytical testing.
• Ability to work effectively in international and multidisciplinary teams, both independently and collaboratively.
• Strong interpersonal, communication, organizational, and time management skills.
• Fluency in English.