Analytical Scientist (m/f/d)

Analytical Scientist (m/f/d) - Pharma / liquid chromatography/detection methodologies/IND / NDA/

Project:
For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Analytical Scientist (m/f/d).

Background:
The Analytical Research & Development department, an integral component of Synthetic Molecules Technical Development, bears global responsibility for the advancement of cutting-edge analytical methodologies, the comprehensive analysis of raw materials, intermediates, active pharmaceutical ingredients, and diverse dosage forms pertaining to synthetic molecule development products, and the meticulous preparation of regulatory documentation for submission to health authorities. In this role you will be joining a highly motivated and experienced team of analytical scientists. You will be responsible for leading analytical development activities for synthetic molecule projects, from early development to commercialization. This is an exciting opportunity to apply your expertise in a dynamic and challenging environment, contributing to the development of life-changing medicines.

The perfect candidate holds a Master's or Ph.D. in chemistry or pharmacy, coupled with a minimum of five years of experience within the pharmaceutical industry. A robust background in analytical development is paramount, with particular expertise in liquid chromatography and diverse detection methodologies. Beyond technical proficiency, the person is an open-minded, goal-oriented individual who demonstrates the ability to thrive within a dynamic environment. The perfect candidate perceives challenges as opportunities for growth and consistently exhibits respectful collaboration with team members, customers, and stakeholders. Furthermore, an excellent command of the English language is a prerequisite.

Tasks & Responsibilities:

• Developing a phase-appropriate control strategy for pharmaceutical dosage forms, encompassing the active ingredient and its precursors.
• Collaborating effectively with stakeholders across various departments, including drug substance and drug product process development and manufacturing, Technical Regulatory Affairs, Quality Assurance, and both internal and external analytical partners (such as service providers and commercial manufacturing/testing/packaging sites).
• Coordinating comprehensive analytical activities, which involves generating physical and chemical data for materials, developing/improving and validating analytical test methods or other analytical controls, generating packaging-specific stability data, and ensuring thorough documentation.
• Coaching technicians on project work and serving as a central point of contact for project related information.

Must Haves:

• A Master's or Ph.D. in chemistry, pharmacy, or a related field
• A minimum of five years (ideally) of professional experience within the pharmaceutical industry
• Profound expertise in analytical development, encompassing formulation development support and the implementation of a control strategy for impurities in Investigational New Drug (IND) and New Drug Application (NDA) filings
• A robust foundation in liquid chromatography (HPLC and UHPLC) with proficiency in various detection methods, including UV, Mass Spectrometry (MS), fluorescence, and charged aerosol detection
• A comprehensive understanding of quality control principles is essential.
• Demonstrated experience in applying Good Manufacturing Practice (GMP) requirements and a clear understanding of their application across different clinical phases.
• Digital acumen to support digital transformation initiatives; familiarity with statistical analysis of analytical data is also advantageous.
• Excellent command of the English language. Proficiency in German is considered a plus.
• Superior communication skills and a proven ability to collaborate successfully.
• Open-minded, goal-oriented, and capable of thriving in a rapidly evolving environment
• Views challenges as opportunities and consistently demonstrates respectful collaboration with team members, customers, and stakeholders, even under pressure

Reference Nr.: 924338OK
Role: Analytical Scientist (m/f/d)
Industrie: Pharma
Workplace: Basel
Pensum: 80-100% (100% preferred)
Start: ASAP (latest Start Date: 01.12.2025)
Duration: 12 months +
Deadline: 06.08.2025

If you are interested in this position, please send us your complete dossier.

About us:

ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering.

We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.