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Analytical Method Development Scientist Jobs in New York

Senior Scientist

Hauppauge, NY · On-site

$90K - $110K/yr

Senior Scientist (R&D) is responsible for method development, validation, and analytical support activities for dietary supplements/pharmaceutical raw materials and finished products in a ...

Senior Scientist

Hauppauge, NY · On-site

$90K - $110K/yr

Senior Scientist (R&D) is responsible for method development, validation, and analytical support activities for dietary supplements/pharmaceutical raw materials and finished products in a ...

Senior Scientist

Hauppauge, NY · On-site

$90K - $110K/yr

Bonus based on performance Senior Scientist (R&D) is responsible for method development, validation, and analytical support activities for dietary supplements/pharmaceutical raw materials and ...

We are seeking a curious, technically capable R&D Scientist to contribute to the development and ... Proficient in utilizing common analytical methods and characterization techniques to evaluate ...

We are seeking a curious, technically capable R&D Scientist to contribute to the development and ... Proficient in utilizing common analytical methods and characterization techniques to evaluate ...

We are seeking a curious, technically capable R&D Scientist to contribute to the development and ... Proficient in utilizing common analytical methods and characterization techniques to evaluate ...

... and Development Scientist position in Valhalla, NY. The incumbent will conduct and support ... analytical test methodologies and data interpretation • Ability to make significant technical ...

Showing results 41-60

Analytical Method Development Scientist information

See New York salary details

$24

$46

$71

How much do analytical method development scientist jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for analytical method development scientist in New York is $46.03, according to ZipRecruiter salary data. Most workers in this role earn between $34.47 and $53.12 per hour, depending on experience, location, and employer.

What does an analytical method development scientist do?

An Analytical Method Development Scientist is responsible for designing, developing, and validating analytical methods used to test and analyze chemical compounds, pharmaceuticals, or other materials. They ensure that the methods are accurate, reliable, and compliant with regulatory standards. This role involves working with advanced laboratory instruments, troubleshooting analytical issues, and documenting procedures for use in research, quality control, or manufacturing environments.

What are the key skills and qualifications needed to thrive as an analytical method development scientist?

To thrive as an Analytical Method Development Scientist, a strong background in chemistry, analytical techniques, and method validation—often supported by a relevant degree in chemistry or pharmaceutical sciences—is essential. Familiarity with laboratory instrumentation such as HPLC, GC, MS, and software for data analysis, as well as knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for success in this role. These skills ensure reliable method development, regulatory compliance, and effective collaboration within multidisciplinary scientific teams.

What are the typical challenges faced by an analytical method development scientist when transferring methods to quality control or manufacturing teams?

One common challenge for Analytical Method Development Scientists is ensuring that newly developed analytical methods are robust and reproducible when transferred to quality control or manufacturing teams. Differences in equipment, sample matrices, or operator technique can impact results, so thorough method validation and clear documentation are essential. Scientists often work closely with cross-functional teams to provide training, troubleshoot issues, and adapt protocols as needed. Successfully managing these transitions helps maintain product quality and regulatory compliance.

What is the difference between Analytical Method Development Scientist vs Analytical Chemist?

AspectAnalytical Method Development ScientistAnalytical Chemist
Primary FocusDeveloping and validating new analytical methodsPerforming routine analysis and testing
Work EnvironmentResearch labs, R&D departmentsQuality control labs, manufacturing facilities
CredentialsBachelor's or Master's in Chemistry or related field; experience in method developmentBachelor's degree in Chemistry or related field; experience in analytical testing

While both roles involve analytical testing, the Analytical Method Development Scientist primarily focuses on creating and validating new analytical methods, often in research settings. In contrast, the Analytical Chemist typically performs routine testing to ensure product quality in manufacturing or quality control labs.

What are popular job titles related to Analytical Method Development Scientist jobs in New York?

For Analytical Method Development Scientist jobs in New York, the most frequently searched job titles are:

What job categories do people searching Analytical Method Development Scientist jobs in New York look for?

The top searched job categories for Analytical Method Development Scientist jobs in New York are:

Infographic showing various Analytical Method Development Scientist job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $95,749 per year, or $46 per hour.

Process Development Engineer III, Analytical Science: Synthetic and Bioconjugation Scale-Up Tech...

Regeneron Pharmaceuticals

Tarrytown, NY • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 days ago


Key responsibilities

  • Independently design and execute analytical testing, method development, and characterization to enable bioconjugate process development

  • Serve as the subject matter expert to lead and design analytical deliverables, including method development, transfer, training, and troubleshooting

  • Connect, interpret, and communicate complex results into clear, actionable next steps for technical and non-technical audiences to drive timely decisions


Regeneron rating

8.5

Company rating: 8.5 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

19th of 86 rated pharmaceutical


Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Process Development Engineer III to join our Preclinical Manufacturing & Process Development (PMPD) organization's Synthetic and Bioconjugation Scale-up Technologies (SBST) Analytics group, on-site in Tarrytown, NY. In this role, you will serve as the analytical lead to develop fit-for-purpose analytical methods, transfer methods, and provide troubleshooting support to advance a diverse bioconjugate pipeline.

This position offers the opportunity to lead and implement analytical deliverables, working closely with bioconjugation teams and internal/external collaborators (CDMOs) to advance bioconjugate programs from development to commercialization.

When & where:
  • Shift Requirements: Full-time, standard business hours
  • Location: On-site in Tarrytown, NY
  • Flexibility & travel: Minimal to no travel; on-site presence required to support lab operations and collaboration with internal/external CDMO partners
What you'll do:
  • Independently design and execute analytical testing, method development, and characterization to enable bioconjugate process development
  • Serve as the subject matter expert to lead and design analytical deliverables: robust method development, method transfer to internal/external receiving labs, training, and troubleshooting to move programs forward
  • Connect, interpret, and communicate complex results into clear, actionable next steps for technical and non-technical audiences to drive timely decisions
  • Author high-quality documentation (e.g., procedures, development and characterization reports, ELN entries) in a timely manner to support program timelines
  • Drive, build, and improve business workflows: documentation standardization, data digitization, and sample management
  • Maintain compliance with lab and environmental safety requirements and promote a safe lab environment
  • Proactively scout, evaluate, and implement new or improved technologies for high-throughput analytics and real-time decision-making
  • Lead equipment upkeep and troubleshooting, maintain an organized workspace, and proactively plan for lab resources
  • Mentor and support peers and junior team members (direct and/or indirect via matrix)
The environment and physical rhythms of this role:
  • This is a hands-on, on-site laboratory role serving as analytical lead across bioconjugate programs, requiring close collaboration with internal teams and external CDMO partners and comfort navigating complex, ambiguous problems.
  • Flexibility to thrive in a fast-paced, highly collaborative environment while independently driving projects forward is required.
Let's find out if we're a fit:Must-haves:
  • B.S. with 10+ years of relevant experience, M.S. with 7+ years, or recent Ph.D. with 0-3 years of relevant experience in chemistry, biochemistry, biology, chemical engineering, or a related field
  • Hands-on experience with analytical method development for antibody, bioconjugate, and/or synthetic molecules (e.g., small molecule, PEG, peptides, and/or siRNA), such as electrophoresis, HPLCs, LC-MS, UV spectroscopy, plus associated software (e.g., Empower)
  • Hands-on experience transferring methods to internal/external labs, and troubleshooting
  • Demonstrated experience serving as an analytical lead for bioconjugate programs, collaborating effectively with internal teams and external CDMOs
  • Strong written and verbal communication skills, including the ability to present data clearly to diverse audiences
  • Experience drafting analytical methods, development, and characterization reports to support regulatory filing
  • Ability to work independently and collaboratively across cross-functional teams to persuade and drive data-based decisions
  • Demonstrated initiative, learning agility, and a growth mindset in a fast-paced environment
Preferred / nice-to-haves:
  • Customer-centric mindset in providing analytical support across different phases of drug development
  • Experience simplifying complex technical messages for varied audiences
Thrive today. Grow tomorrow.
  • Student Loan Paydown program & Tuition Reimbursement
  • Family Care Benefits
  • Relocation Assistance
  • Inclusion, Culture and Well-Being programs (including physical & mental health)

#pmpd

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$109,900.00 - $179,300.00

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