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Jobs · Analyst · North Carolina

Senior Scientist 2-Analytical Research and Development

Cambrex · High Point, NC · 1 wk ago
AnalystFull-time

About Cambrex

Cambrex is a leading global contract development and manufacturing organization (CDMO) providing drug substance, drug product, and analytical services across the entire drug lifecycle. With over 40 years of experience and a team of more than 2,000 professionals, Cambrex serves global clients in branded and generic markets for API and dosage form development and manufacturing.

We strive to build a culture where colleagues engage in meaningful work, learn new skills, enjoy safe and engaging experiences, and strengthen connections with coworkers and the community. Cambrex offers a competitive benefits package, including healthcare, life insurance, and retirement planning.

About the Role

This position involves developing and optimizing analytical methods for intermediates and final products, particularly where some parameters are already established. The role includes maintaining laboratory instrumentation, troubleshooting HPLC and GC issues, and supporting the Process Chemistry department with analytical needs for process development and manufacturing.

Responsibilities

  • Develop and optimize robust, validatable analytical methods for intermediates and final products.
  • Maintain and review laboratory notebooks and data entries.
  • Write analytical procedures, protocols, reports, and similar documents.
  • Perform and lead laboratory investigations for Analytical and QC with minimal support.
  • Participate in larger-scope projects and act as Analytical lead for internal projects.
  • Train and mentor laboratory colleagues.
  • Maintain laboratory equipment and troubleshoot HPLC, GC, LC/MS, and GC/MS issues.
  • Ensure compliance with Company SOPs and regulatory guidances.
  • Handle hazardous materials and wastes, recognizing emergency situations.

Requirements

  • Ph.D. in Chemistry or related field with a minimum of 2 years of experience, or
  • M.S. in Chemistry or related field with a minimum of 6 years of experience, or
  • B.S. in Chemistry or related field with a minimum of 10 years of experience in a laboratory environment.

Skills & Qualifications

  • Analytical Chemistry Knowledge: Strong understanding of analytical chemistry principles with practical laboratory experience.
  • Cross-Discipline Knowledge: Good understanding of organic chemistry and engineering principles.
  • GMP/Regulatory Knowledge: Demonstrated understanding of GMP and ability to advise on regulatory strategies with minimal manager input.
  • Instrumentation: Proficient in using, training, and troubleshooting HPLC, GC, and MS; working knowledge of FTIR, NMR, XRPD, laser diffraction particle size, and other pharmaceutical analytical equipment.
  • Communication: Strong written and oral communication skills; able to handle client requests with manager review.
  • Problem Solving: Ability to lead investigations and solve workplace problems with manager support.
  • Time Management: Strong self-organization and time management skills.
  • Leadership: Demonstrated ability to share ideas, mentor colleagues, and organize group initiatives.
  • Technical Documentation: Ability to write and review technical documents with minimal errors.

Work Environment

  • Sedentary work, occasionally exerting up to 10 pounds of force.
  • Daily work involves both office settings and laboratory environments, requiring walking, standing for extended periods, visual acuity, talking, and computer typing.
  • All requirements are subject to reasonable accommodations for individuals with disabilities.

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