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Analytical Scientist - Structural Characterization

Job in Harvard, Worcester County, Massachusetts, 01451, USA
Listing for: Veranova
Full Time position
Listed on 2025-12-07
Job specializations:
  • Science
    Research Scientist, Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 90000 - 135000 USD Yearly USD 90000.00 135000.00 YEAR
Job Description & How to Apply Below
Location: Harvard

Analytical Scientist - Structural Characterization

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Discover Veranova:

At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.

Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.

Role Overview

The Structure Characterization Analytical Scientist will have expertise in structural elucidation of drug substances, impurities and degradants through rapid and efficient characterization of synthetic molecules by NMR, chromatography and mass spectrometry analysis. The successful candidate will have a strong foundation in analytical chemistry and spectroscopy, with hands‑on laboratory experience. A background in organic chemistry is highly desirable for interpreting complex structures and reaction mechanisms.

Core

Responsibilities
  • Exercise sound technical judgment in the planning, execution, and analysis of experiments to determine structural identification of pharmaceutical actives and related substances including forced degradation for impurity enrichment, 2D NMR, high‑resolution MS, HPLC and GC method development.
  • Implement characterization approaches for the preparation, isolation, and identification of low‑level impurities in a drug development environment.
  • Author analytical test methods, protocols, reports, relevant SOPs and regulatory documents as needed.
  • Develop and apply qNMR methods for accurate quantification of drug substances and impurities.
  • Support method development, qualification, transfer, and validation activities for analytical procedures.
  • Provide support for cGMP manufacturing campaigns, ensuring compliance with regulatory requirements and documentation standards.
  • Communicate technical findings and results to both internal and external stakeholders, including clients and regulatory bodies.
  • Collaborate with key partners including chemistry development scientists, quality control and regulatory affairs teams to ensure successful project delivery.
  • Mentor and develop scientific staff. Ensure continued technical and professional growth of department members, encourage efforts towards excellence and knowledge sharing.
  • Maintain and troubleshoot NMR and LCMS instrumentation (e.g., Orbitrap, Q‑TOF, Triple Quad).
Qualifications
  • Ph.D. or M.S. in Analytical Chemistry, Organic Chemistry, Pharmaceutical Sciences, or related field. Demonstrated mastery of one or more subject areas related to structural characterization.
  • Strong hands‑on experience with 2D NMR, HR-MS.
  • 3+ years of hands‑on experience in structural characterization of impurities for active pharmaceutical ingredients under cGMP’s.
  • Strong knowledge of organic structure elucidation – forced degradation, MS, NMR, etc., with the ability to train/mentor colleagues.
  • Excellent communication, organizational, and leadership skills with ability to work independently and in a team environment.
  • Well organized with good problem‑solving skills, a high level of attention to detail and a passion for delivering high quality data in a fast‑paced environment.
Preferred
  • Experience with regulatory submissions and GMP/GLP environments.
  • Experience with structural characterization of larger synthetic molecules including peptides and oligonucleotides.
  • Risk assessment and development of trace level methods for potential GTI and nitrosamines.
Salary Range

$90,000 – $135,000 annual base salary

Our Commitment
  • Health & Wellness:
    Comprehensive health & wellness benefits. Access to mental health resources and wellness programs.…
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