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Lonza

Supervisor Analytical Chemistry

Bend, OR · On-site

... Europe, North America, and Asia. Summary Lonza Pharma & Biotech is currently seeking a Supervisor ... The Supervisor, Analytical Chemistry will provide leadership guidance and successful execution of ...

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Supervisor Analytical Chemistry

Lonza

Bend, OR • On-site

Full-time

Re-posted 25 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

Job description

Company Description
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.
Job Description
Job Description Summary
Lonza Pharma & Biotech is currently seeking a Supervisor, Analytical Chemistry for our rapidly growing site in Bend, Oregon.
The Supervisor, Analytical Chemistry will provide leadership guidance and successful execution of analytical development and quality control functions across the drug product lifecycle for commercial distribution). The successful candidate will have a strong chemistry background and demonstrate leadership behaviors required to lead successful teams and maximize results.
We're looking for a Supervisor that possesses an enthusiasm for science, who wants to bring their outstanding problem-solving skills into a fast-paced environment.
Responsibilities include but are not limited to:
  • Create and manage schedules for day-to-day lab activities
  • Write, review and approve test notes, specifications, and analytical test reports
  • Manage project-specific analytical and stability studies
  • Ensure data is managed and evaluated, including the creation, review and trending of stability results
  • Organize and execute stability shipments to off-site storage and/or laboratory facilities for testing
  • Preparation and review of Sampling and Testing Plans, stability calendars, protocols and reports
  • Distribution of projects and continuous improvement tasks and track progress
  • Coordinate as needed for the stability chambers
  • Demonstrate high standard of ethics, integrity and professionalism
  • Continuously identify more effective ways to drive performance
  • Partner with colleagues across functions to build trust, inspire others and drive results

Qualifications:
  • Bachelor's Degree in a scientific or related field is required
  • Experience in a GMP pharmaceutical laboratory and stability setting is preferred
  • Knowledge of analytical instrumentation (HPLC, GC, KF, PSD)
  • Experience in supervising others is preferred
  • Must have experience as an Analyst or Chemist

Qualifications
Additional Information
All your information will be kept confidential according to EEO guidelines.

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