Cambrex Corporation

Senior Associate Scientist / Scientist (Analytical R&D)

Cambrex Corporation$74K — $110K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS or MS in Chemistry with 3-5+ years, or PhD with 0+ years of experience in analytical chemistry.
  • Expertise in method development for analytical techniques like (U)HPLC, GC, LC/MS, and NMR.
  • Knowledge of regulatory guidelines and GMP standards is essential.
  • Strong written and oral communication skills required.
  • Experience in quality control testing and cross-site collaboration is preferred.
  • Experience in peptide or oligonucleotide analysis is a plus.
  • Strong problem-solving and organizational skills needed.

Responsibilities

  • Develop and optimize analytical methods for pharmaceutical compounds.
  • Utilize a range of analytical techniques for characterization and quantification.
  • Perform various physical/chemical property tests and moisture content analysis.
  • Conduct compendial tests to support product compliance and stability.
  • Review and author analytical protocols and compliance documents.
  • Lead method transfers and ensure technical alignment with partners.
  • Engage in cross-site collaborations to maintain project continuity.

Benefits

  • Collaborative and innovative work environment with a focus on entrepreneurial tasks.
  • Potential for technical leadership opportunities and mentoring roles.
  • Engagement with clients for direct communication and feedback.
  • Access to cutting-edge analytical technologies and methods.
  • Dynamic work setting that encourages quick problem resolution.
Full Job Description
Job Overview Snapdragon Chemistry is seeking exceptional candidates for the position of Senior Associate Scientist or Scientist in our Analytical R&D group. The successful candidate will join a team of innovative and entrepreneurial scientists dedicated to providing high-quality analytical support for synthetic process development projects. We are looking for a candidate who has a passion for working in a fast-paced, dynamic environment. The ideal candidate will hold at least a BS or MS in Chemistry with 3-5+ years of experience, or a PhD with 0+ years of experience in analytical chemistry within the pharmaceutical industry. The candidate should have a broad experience of method development of analytical technologies such as (U)HPLC, GC, KF, LC/MS, NMR, TGA, DSC, particle size analyzer etc. to characterize and quantitate pharmaceutical synthetic molecules. Knowledge of regulatory guidelines and experience in quality control testing are preferred. Candidates must possess strong written and oral communication skills. Responsibilities
  • Develop, optimize, and qualify analytical methods for pharmaceutical intermediates, APIs, and high-value specialty chemicals.
  • Utilize analytical techniques, including (U)HPLC, GC, KF, LC/MS, NMR, TGA, DSC, particle size analysis, and wet chemistry assays.
  • Perform moisture content testing (e.g., Karl Fischer) and other physical/chemical property determinations.
  • Conduct USP and other compendial tests as required to support product release, stability, and compliance.
  • Author and review analytical protocols, reports, and SOPs in compliance with GMP and regulatory expectations.
  • Conduct GMP testing and documentation in support of batch release, stability studies, and method transfer activities.
  • Lead and execute method transfers between internal teams and external partners, ensuring technical alignment and smooth execution.
  • Engage in cross-site technical interactions, including collaborative work with Cambrex sites, to align analytical strategies and ensure project continuity.
  • Manage outsourced analytical testing at third-party laboratories, including project scoping, technical oversight, and data review.
  • Ensure all analytical work meets cGMP standards and company quality system requirements.
  • Maintain a strong sense of urgency to meet project timelines and client deliverables without compromising quality.
  • Communicate directly with clients to provide project updates, interpret results, address technical inquiries, and present analytical strategies and timelines.
  • Provide technical leadership, mentor junior scientists, and contribute to best practices in method development, validation, GMP compliance, and compendial testing.
Qualifications/Skills
  • Proven experience in method development, validation, troubleshooting, and transfer for pharmaceutical synthetic molecules.
  • Broad expertise in analytical instrumentation, wet chemistry techniques, and data interpretation.
  • Experience performing moisture analysis (Karl Fischer) and other USP compendial tests.
  • Strong working knowledge of GMP requirements, ICH guidelines, and regulatory expectations (FDA, EMA).
  • Experience in quality control testing, stability programs, outsourced testing management, and cross-site collaboration preferred.
  • Peptide and/or oligonucleotide analytical experience is a plus but not required.
  • Demonstrated ability to work with urgency while maintaining accuracy and compliance.
  • Strong organizational, problem-solving, and communication skills (written and oral).
  • Ability to interact confidently with clients and work effectively in a fast-paced, multi-project environment.
Education, Experience & Licensing Requirements
  • For the Senior Associate Scientist role, a BS or MS in chemistry or related field with 3-5+ years of experience is required. Pharmaceutical GMP experience is required.
  • For the Scientist role, a BS, MS with 5-7+ years of experience or a PhD in chemistry or related field with 0+ years of experience is required. Pharmaceutical GMP experience is desired.
The estimated salary range of $74,000 - $92,000 reflects an anticipated range for the Senior Associate Scientist, ARD position. The estimated salary range of $92,000 - $110,000 reflects an anticipated range for the Scientist, ARD position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, and certifications or other professional licenses held. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

About Cambrex Corporation

Cambrex Corporation is a life sciences company that provides products and services for small molecule active pharmaceutical ingredients (APIs). The company's products and services are used in the development and commercialization of new and generic therapeutics. Cambrex operates through three segments: Small Molecule API, Biologic API, and Finished Dosage Formulations. The Small Molecule API segment provides APIs for branded and generic drugs, while the Biologic API segment provides biologically derived APIs. The Finished Dosage Formulations segment provides finished dosage forms of solid, semi-solid, and liquid products. Cambrex serves customers in the United States, Europe, and Asia.
Learn more about Cambrex Corporation
Size
11 employees
Industry
NASDAQ

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