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Lead Chemical Process R&D Scientist (m/f/d)

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Onsite

Lead Chemical Process R&D Scientist (m/f/d)

Randstad Switzerland

Lead Chemical Process R&D Scientist (m/f/d)

Skills

RCompliance

14 days ago

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Important information


Contract type:

Freelance / Contract

Location:

Basel, Switzerland

Work mode:

Onsite

Published on:

14 October 2026

What they need


For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a dedicated Lead Chemical Process R&D Scientist

In this function you will lead chemical process R&D activities to deliver safe, scalable, efficient and sustainable processes as well as drug substance material for projects in clinical development, with a focus on late stage development, leveraging internal and external CDMO capabilities.

General Information:

  • Start date: ASAP
  • Latest start date: February 2027
  • Duration: 1 year
  • Extension: likely
  • Contract type: Temporary contract via Randstad (employment)
  • Work location: Basel
  • Workload: 100%
  • Home Office: 2 days/week
  • Working hours: Standard
  • Travel: possibly to visit CDMOs, up to 4x/year - Europe or Asia (China, India)

Tasks & Responsibilities:

  • Lead Internal & External Chemical Process R&D activities: Direct chemical process research and development work, managing an internal team of 1–5 process chemists and/or leading external activities at contract development and manufacturing organizations (CDMOs).
  • Oversee end-to-end process chemistry workflows, including synthetic route scouting, process optimization, scale-up, and support for supply activities.
  • Coordinate Cross-Functional Delivery: Synchronize internal laboratory efforts with CDMO timelines to guarantee the timely, safe, and cost-effective production of active pharmaceutical ingredients (APIs) and advanced intermediates
  • Ensure Quality & Compliance: Deliver the target compounds following internal quality processes and according to specifications, safety standards and sustainability objectives.

Must Haves:

  • PhD or Postdoctoral background in Synthetic Organic Chemistry .
  • 5+ years of hands-on experience in pharmaceutical chemical process R&D , with demonstrated expertise in late-stage process development and scale-up.
  • Leadership & Project Management: Proven track record of leading, mentoring, and driving project deliverables within internal process chemistry teams.
  • CDMO Management: Direct experience managing external chemical development, technology transfers, and manufacturing activities at CDMOs.
  • Technical & Software Proficiency: High proficiency with standard office applications alongside core chemistry tools, including chemical drawing tools, literature/patent search engines, Design of Experiments (DoE) applications, analytical software, and project planning platforms.
  • Professional fluency in spoken and written English .

Nice to Have:

  • Familiarity or prior experience working within Good Manufacturing Practice (GMP) environments.
  • Professional working proficiency or fluency in German.
  • Proficiency in the use of kinetic modeling or scale-up simulation software.

Sounds interesting? Apply now – we’re looking forward to receiving your applications!

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