(Senior) Scientist (all genders) Quality Control, Physico-Chemical Analytics

at  Lonza

Visp, VS, Switzerland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate02 Jan, 2025Not Specified04 Oct, 20244 year(s) or aboveChemistry,Pharmaceutical Sciences,Pharmaceutical Industry,Creativity,Life Sciences,BiochemistryNoNo
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Description:

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
For our site in the beautiful town of Visp, we are looking for (Senior) Scientist (all genders) for our Quality Control Team.

KEY REQUIREMENTS :

  • MSc or PhD in Chemistry, Biochemistry or Pharmaceutical Sciences is required
  • Experience with physico-chemical techniques is an advantage
  • Work experience in the pharmaceutical industry (especially in Quality Control) is highly preferred
  • GMP knowledge is a plus
  • Fluent in either English or German language is a must (knowledge in the respective other language is an advantage)
    Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
    People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference

Responsibilities:

  • Review of data from the Physico-Chemical Quality Control Laboratory
  • Writing Laboratory investigations, corrective and preventative measures etc
  • Defining cGMP examinations in the event of deviations
  • Support process improvements within Quality Control group
  • Readiness for on-call duty (ca 4 - 5 weeks per year, assignments can be carried out remotely)


REQUIREMENT SUMMARY

Min:4.0Max:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

MSc

Chemistry

Proficient

1

Visp, VS, Switzerland