Supervisor Analytical Chemistry

Lonza; North Bend (OR); On-site; Confidential; Full time

Job summary

Lonza in North Bend, Oregon, is looking for a Supervisor in Analytical Chemistry to lead analytical development and quality control functions across the drug product lifecycle. The ideal candidate will have a Bachelor's degree in a scientific field and experience in GMP pharmaceutical environments.

This role involves creating lab activity schedules, managing analytical studies, and ensuring data integrity. If you are enthusiastic about science and problem-solving in a fast-paced environment, this position may be for you.

Qualifications

• Experience in a GMP pharmaceutical laboratory and stability setting is preferred.
• Experience in supervising others is preferred.
• Must have experience as an Analyst or Chemist.

Responsibilities

• 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.

Skills

Leadership behavior

Analytical skills

Problem-solving

Education

Bachelor's Degree in a scientific or related field

Tools

HPLC

GC

KF

PSD

Job description

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

• 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

Additional Information

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