Senior Scientist, Analytical Development, DPS
vor 5 Tg.

At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success.

Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia.

Our vision :

We strive to be the leading supplier using science and technology to improve the quality of life.

Our mission :

We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.

Do you want to help us as we shape the future of this great organization?

Job Description Summary

For DPS (Drug Product Services) in Basel Switzerland, we have open multiple opportunities for a Senior Scientist in our growing Analytical Development team.

Working closely with Quality Control and Formulation Development, this team offers specialized services solutions for customers.

Become part of this exciting opportunity by applying for the position of Senior Scientist Analytical Development.

Key Accountabilities and Duties :

  • Help establish DP analytical infrastructure and services for biologics, small molecule and peptide parenteral products for clinical and commercial products
  • Install, qualify and maintain instruments for DP Phys-Chem Analytics and QC in close alignment with current best practices and regulations
  • Develop and establish analytical methods and technologies to support formulation development and DP QC (specifically including HPLC and CE purity methods, content by UV, identity, color, clarity and opalescence, pH, osmolality, extractable volume, CCI, visual inspection, subvisible particles and related DP analytics).
  • Carry out phys-chem analytical tests to support formulation development and DP QC as required, possibly under GMP, following applicable SOP’s and all current documentation practices.
  • Ensure proper maintenance of equipment, safety and health protection following lab and safety instructions and all cGMP regulations
  • Evaluate and implement new methods and technologies, as required; participate and contribute to innovation, technical strategy projects and scientific publications
  • Perform other duties as assigned.
  • Qualifications and skills required :

  • A degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences (or related subject) or a training on the job as analytical lab technician
  • 2 years of experience as a research or technical assistant in the pharmaceutical or chemical industry, preferably in analytics
  • Good working knowledge in relevant analytical techniques
  • Experience with parenteral dosage forms and protein analytics
  • Good reporting, interpretation and documentation of scientific results
  • Excellent communication skills
  • Ability to work independently and in a team environment
  • Detail oriented
  • Good inter-personal skills
  • Enthusiastic and open-minded
  • Willingness to learn and carry out new and complex tasks
  • Proactive attitude
  • Good knowledge of written and spoken English
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