Senior Scientist Analytical Project Manager

vor 10 Stunden


Basel, Basel-Stadt, Schweiz Work Selection AG Vollzeit

At Work Selection AG, we are seeking a highly skilled and motivated Technical Analytical Project Leader Scientist to join our team in Basel, Switzerland.

About Us

We are an international organization with a global presence, committed to developing meaningful medicines for patients. Our Global Technical Development (PTD) group is an integral part of this mission, actively collaborating and developing creative technical solutions to bridge early-stage, late-stage, and commercial product needs.

Our mandate is to reliably deliver the pipeline and supply quality products to patients, exceling through innovation, teamwork, dedication, and mutual respect.

About the Role

This temporary contract will last for 12 months, with the option to extend. As a Technical Analytical Project Leader Scientist, you will be responsible for covering all analytical aspects during the project development lifecycle, working closely with peers, lab technicians, and cross-functional partners from various disciplines.

You will plan and document your experiments/results independently, prepare for regulatory submissions such as IND and NDA, and collaborate with stakeholders from different disciplines, varying with the clinical phase of the project.

The ideal candidate will have a Master's or Ph.D. in chemistry, pharmacy, biotechnology, or biochemistry, with a minimum of 3 years' professional experience in the pharmaceutical industry. Experience in analytical development with Oligonucleotides, Peptides, biologically derived molecules, and their advanced formulations is a plus.

The role requires strong quality mind-set and excellent attention to detail, with experience in applying GMP requirements where necessary. You should also be open-minded, goal-oriented, and able to work in a fast-developing environment, respectfully collaborating with team members, customers, and stakeholders.

Key Responsibilities
  • Cover all analytical aspects during the project development lifecycle
  • Work in close collaboration with peers, lab technicians, and cross-functional partners from various disciplines
  • Plan and document your experiments/results independently
  • Prepare for regulatory submissions such as IND and NDA
  • Collaborate with stakeholders from different disciplines, varying with the clinical phase of the project
Requirements
  • Master's or Ph.D. in chemistry, pharmacy, biotechnology, or biochemistry
  • Minimum 3 years' professional experience in the pharmaceutical industry
  • Experience in analytical development with Oligonucleotides, Peptides, biologically derived molecules, and their advanced formulations is a plus
  • Strong quality mind-set and excellent attention to detail
  • Experience in applying GMP requirements where necessary
Languages

Fluent in English, German is a plus.

We value diversity and welcome applications from all candidates regardless of gender, social origin, religion, age, and identity. We use only one gender form for easier readability and understanding, but all forms are equally intended in context.



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