We are currently looking for a Principal Scientist Tech Ops (CMC Science) to join our global team in Bern.

Key Responsibilities

• Contribute to the development and implementation of phase‑appropriate CMC strategies.
• Support CMC activities for assigned programs from early development through late‑stage clinical development.
• Identify risks and develop mitigation strategies to ensure timelines and quality standards are met.
• Support drug substance and drug product development activities.
• Support analytical method development, validation, and specification setting.
• Support process characterization, validation, and lifecycle management.
• Manage relationships with CDMOs and manufacturing partners.
• Support technology transfer and scale‑up activities.
• Ensure compliance with GMP requirements.
• Author, review, and contribute to CMC sections of regulatory submissions (IND, CTA, NDA, BLA).
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