Analytical Associate in Analytical Development for Synthetic Molecules 100 % (m/w/d)
For our client, F. Hoffmann-La Roche, in Basel, we are looking for a candidate for a long-term temporary assignment via Gi Group.
Analytical Associate in Analytical Development for Synthetic Molecules 100 % (m/w/d)
Background
Pharma Technical Development (PTD) is a global team driving innovation in medicine. Within PTD, PTDC focuses on drug substance, product, and analytics for synthetic molecules. This role supports clinical and commercial supply through advanced analytical methods like HPLC, GC, IC, and MS. Join us to lead innovation in analytical development and help deliver impactful therapies to patients worldwide.
The Perfect Candidate: holds a solid vocational qualification or a bachelor's degree in Analytical Chemistry, Biochemistry, Biotechnology, or a related field, with 1-3 years of hands-on experience in analytical method development within the pharmaceutical industry. They are proficient in analytical techniques such as HPLC, GC, and KF, apply GxP principles confidently, and possess strong scientific writing and documentation skills. With an innovative and quality-driven mindset, they demonstrate adaptability, digital fluency, reliability, and a proactive, collaborative approach in a dynamic environment.
General Information
- Start Date: 01.12.2025
- Latest Possible Start Date: 01.01.2026
- Planned Duration of Employment: 12 months
- Workload: 100%
- Workplace: Basel
- Working Hours: Standard
- Important: Criminal record extract with no entries
Tasks & Responsibilities
- Development, improvement and validation of analytical methods for the quality assessment of starting materials,intermediates, reaction monitoring, active substances and galenical forms
- Thorough and efficient planning, execution and documentation of experiments in collaboration with the relevant team members, analytical project lead and your supervisor, following current GxP guidelines as well as the relevant SOP's
- Work on end to end processes in close collaboration with other associates, scientists, and partners from other departments to ensure efficient analytics and continuous improvement
- Coordination of analytical activities including sample management for the development of synthetic products
- Authoring of documents, e.g. analytical procedures, and validation reports
- Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phases
Must Haves
- You hold a solid vocational qualification with at least 1-3 years' experience in the pharmaceutical industry with a strong focus on analytical methods development (i.e. chromatography) or a bachelor's degree (Analytical Chemistry, Biochemistry, Biotechnology or related field). The role does not require any further academic qualifications
- Hands-on experience in analytical instrumentation and techniques (e.g. HPLC, GC, KF)
- Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phases
- Excellent command of English. Good command of German would be a plus
- A strong interest / background in analytical methods development
- A good scientific writing style and good documentation practice for utilization of corresponding data in regulatory filings
- Excellent digital skills and innovative mindset
- Preparedness to learn, continuously improve and apply novel ideas, tools and processes to quickly adapt to a fast changing environment
- Self-motivated, open-minded, proactive, reliable, goal-oriented and an excellent team player
- A strong quality mindset and excellent attention to detail
Your Application
Please apply online or by email For more information about the position, your GI recruiter, Ms. Heidi Arbogast (+41 61 270 80 26), will be happy to assist you.