Lonza America Inc

Supervisor Analytical Chemistry

Lonza America Inc$80K — $110K *
Bend, OR 97701In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in a scientific field required
  • Preferred experience in a GMP pharmaceutical laboratory
  • Knowledge of analytical instrumentation (HPLC, GC, KF, PSD)
  • Supervisory experience preferred
  • Prior experience as an Analyst or Chemist is essential

Responsibilities

  • Create and manage day-to-day lab schedules
  • Write, review, and approve analytical test reports
  • Manage project-specific analytical and stability studies
  • Ensure proper data management and evaluation
  • Organize stability shipments to external facilities
  • Prepare and review Sampling and Testing Plans
  • Coordinate for stability chambers and track project progress

Benefits

  • Opportunity for leadership development
  • Access to cutting-edge analytical technology
  • Fast-paced and dynamic work environment
  • Collaboration across multi-functional teams
  • Focus on continuous improvement and innovation
Full 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

About Lonza America Inc

Lonza America Inc is a subsidiary of Lonza Group, a Swiss multinational company that provides products and services to the pharmaceutical, biotech, and specialty ingredients markets. Lonza America Inc is responsible for the North American market and offers a range of products and services, including custom manufacturing, research and development, and quality control testing. The company has a strong focus on sustainability and has implemented various initiatives to reduce its environmental impact. Lonza America Inc was founded in 1897 and has since grown to become a leading provider of products and services in the pharmaceutical and biotech industries.
Learn more about Lonza America Inc
Size
16,218 employees
Industry
NASDAQ

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