Neurocrine Biosciences, Inc.

Senior Scientist, Analytical Development (Large Molecule)

Neurocrine Biosciences, Inc.$130K — $179K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • BS/BA in Analytical Chemistry/Cell & Molecular Biology or related field with 12+ years of experience; MS/MA with 10+ years; or PhD with 4+ years of relevant experience.
  • Demonstrated expertise in analytical development and characterization of peptides and bioconjugates.
  • Hands-on experience in method development, optimization, and transfer of analytical methods.
  • Proficient in capillary electrophoresis, iCIEF, LC techniques (RP, SEC, IEX).
  • Excellent communication skills with the ability to collaborate across functions.
  • Strong problem-solving and data interpretation skills, especially for complex analytical challenges.
  • Working knowledge of cGMP principles and relevant regulatory expectations.

Responsibilities

  • Lead analytical development for peptides and bioconjugates using advanced techniques.
  • Independently develop and validate analytical methods for drug candidates.
  • Serve as analytical lead on cross-functional project teams, ensuring timely deliverables.
  • Design and execute laboratory studies with thorough documentation and safety practices.
  • Apply innovative analytical approaches to solve method development challenges.
  • Support analytical method transfer and collaborate with external partners or contract labs.
  • Communicate scientific findings clearly to various stakeholders.

Benefits

  • Retirement savings plan with company match.
  • Paid vacation, holiday, and personal days.
  • Paid parental and medical leave.
  • Comprehensive health benefits including medical, prescription, dental, and vision coverage.
Full Job Description
About the Role:
This position will serve as an analytical lead with a focus on peptides and bioconjugates, supporting drug substance and drug product development from preclinical through commercialization. The successful candidate will develop, establish, qualify/validate, and transfer analytical methods used to characterize and control raw materials, in-process materials, intermediates, drug substance, and drug product. The individual will independently conduct laboratory studies for the characterization of drug candidates, support formulation and process development, and contribute to CMC development and regulatory activities. Work will be conducted in alignment with cGMP principles, safety requirements, and applicable regulatory expectations.

Your Contributions (include, but are not limited to):
  • Lead analytical development and characterization activities for peptides, antibodies, and bioconjugates, using techniques such as capillary electrophoresis, iCIEF, LC (e.g., RP, SEC, IEX), mass spectrometry, and other relevant characterization technologies
  • Independently develop, optimize, qualify, validate, and transfer analytical methods in support of programs from preclinical development through commercialization
  • Serve as an analytical lead on cross-functional project teams and maintain accountability for analytical deliverables supporting CMC, process development, formulation development, and manufacturing activities
  • Independently design, execute, analyze, and interpret laboratory work while ensuring appropriate documentation and safe laboratory practices
  • Apply scientific expertise and develop innovative analytical approaches to address complex characterization and method-development challenges
  • Support analytical method transfer, external testing, manufacturing activities, and interactions with contract laboratories and other external partners
  • Leverage scientific literature, ICH and other regulatory guidance, and practical experience to inform analytical development and CMC strategies
  • Contribute to departmental scientific capabilities, best practices, policies, and strategies
  • Build effective internal and external scientific relationships and collaborate across functions
  • Clearly communicate and present scientific findings, conclusions, and recommendations to audiences across the organization
  • Other duties as assigned


Requirements:
  • BS/BA in Analytical Chemistry/Cell & Molecular Biology or related discipline and 12+ years of experience in the analytical/pharmaceutical development field. Experience in method transfer and validation in Analytical Chemistry; OR
  • MS/MA in Analytical Chemistry or related discipline and 10+ years of experience; OR
  • PhD in Analytical Chemistry or related discipline and 4+ years of relevant experience; may include postdoc experience
  • Demonstrated experience in analytical development and characterization of peptides, antibodies, bioconjugates, and/or other complex modalities
  • Strong hands-on experience in analytical method development, optimization, qualification/validation, and transfer
  • Proficiency with relevant analytical characterization techniques, including capillary electrophoresis, iCIEF, and LC (e.g., RP, SEC, IEX)
  • Additional experience with LC-MS, peptide mapping, SDS-PAGE, ELISA, cell-based potency assays, and glycoprotein/carbohydrate characterization is a plus
  • Experience supporting drug substance and/or drug product development, including process development, formulation development, process characterization, or stability programs
  • Excellent interpersonal, written, and oral communication skills, with demonstrated ability to work effectively on cross-functional teams
  • Strong scientific problem-solving and data interpretation skills, with the ability to independently investigate complex analytical challenges
  • Working knowledge of cGMP expectations applicable to analytical development of drug substance and drug product
  • Knowledge of applicable FDA, EMA, and ICH regulatory expectations and guidance


#LI-LS1

The annual base salary we reasonably expect to pay is $130,800.00-$179,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

About Neurocrine Biosciences, Inc.

Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company dedicated to discovering, developing and delivering life-changing treatments for people with serious, challenging and under-addressed neurological, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis* and uterine fibroids*, with three pivotal and five early-stage clinical programs in multiple therapeutic areas. (*in collaboration with AbbVie)
Learn more about Neurocrine Biosciences, Inc.
Size
900 employees
Market Cap
$11.6 billion
Industry
Net Income
$407.3 million
5 Year Trend
+137.5%
Revenue
$1 billion
NASDAQ

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