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Client Project Manager - Life Sciences, Temporary

Solvias

Kaiseraugst · On-site Mid Level Today

About the role

Position

25068 Client Project Manager - Life Sciences, Temporary for 12 months

Location

Kaiseraugst

About Us

Solvias is a global provider of chemistry, manufacturing, and control (CMC) analytics to the life sciences industry. Our expert team combines decades of experience with regulatory expertise across small molecules, biologics, and cell and gene therapies. Solvias offers end‑to‑end solutions from raw material testing to drug product release and API development for small molecules. Headquartered near Basel, Switzerland, Solvias operates six global Centers of Excellence, all adhering to the highest ISO, GMP, GLP, and FDA standards.

Responsibilities

  • Lead and coordinate customer projects within the CRO/CDMO environment from start to finish
  • Serve as the primary point of contact for customers and promote customer satisfaction through professional, solution-oriented communication
  • Align project goals and deliverables with internal and external stakeholders
  • Monitor timelines, budgets, risks and overall progress to ensure successful project execution
  • Manage and maintain project documentation and data in internal systems
  • Ensure compliance with contracts, quality standards (GMP), and internal processes
  • Track and report KPIs and support continuous improvement initiatives

Qualifications

  • Bachelor’s or Master’s degree in Life Sciences (or a related field), with relevant experience in project management in a life science organization or a similar role
  • Proven track record of building and maintaining long‑term, trust‑based customer relationships
  • Excellent communication and stakeholder management skills
  • Strong commercial awareness and a solution‑oriented mindset
  • Ability to lead cross‑functional teams and drive global collaboration
  • Deep understanding of analytical drug development, clinical trial processes, regulatory requirements and industry standards

Reference

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Requirements

  • Proven track record of building and maintaining long‑term, trust‑based customer relationships
  • Excellent communication and stakeholder management skills
  • Strong commercial awareness and a solution‑oriented mindset
  • Ability to lead cross‑functional teams and drive global collaboration
  • Deep understanding of analytical drug development, clinical trial processes, regulatory requirements and industry standards

Responsibilities

  • Lead and coordinate customer projects within the CRO/CDMO environment from start to finish
  • Serve as the primary point of contact for customers and promote customer satisfaction through professional, solution-oriented communication
  • Align project goals and deliverables with internal and external stakeholders
  • Monitor timelines, budgets, risks and overall progress to ensure successful project execution
  • Manage and maintain project documentation and data in internal systems
  • Ensure compliance with contracts, quality standards (GMP), and internal processes
  • Track and report KPIs and support continuous improvement initiatives

Skills

GMP

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