Neurocrine Biosciences Inc. Posted September 10, 2026

Senior Scientist, Analytical Development (Large Molecule)

US CA San Diego, United States Full time
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Neurocrine Biosciences Inc. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Who We Are:

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit  neurocrine.com , and follow the company on  LinkedIn ,  X , Facebook and YouTube . ( *in collaboration with AbbVie )

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 6+ 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 4+ years of experience; OR

PhD in Analytical Chemistry or related discipline and 2+ 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

Neurocrine Biosciences is an EEO/Disability/Vets employer.

We are committed to building a workplace of belonging, respect, and empowerment , and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don’t line up to exactly what we have outlined in the job description.

_

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.

Job details

Seniority
Senior
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
US CA San Diego, United States
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 489 comparable Senior Manufacturing & CMC roles across 75 biopharma companies.

489Comparable roles tracked
477Currently active
75Companies hiring similar roles
31Countries represented

Salary context

207 of 489 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $130,800/yr – $179,000/yr
Lowest disclosed · Associate Director, Digital Scientific Workflows · Merck $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Senior Principal Scientist, Upstream Process Development Group Lead · Merck $190,800/yr – $300,300/yr
Peer group range $0 – $245,550 (median $150,600)

Where these roles are based

Top locations among the 489 comparable roles

United States325
India38
Netherlands20
Ireland16
United Kingdom9
Singapore8

+ 25 more countries

Seniority mix

489 of 489 peers have a known seniority level

Senior323
Principal92
Associate Director74

Therapeutic area mix

2 of 489 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease2

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.