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Method Development Scientist Jobs in New Jersey (NOW HIRING)

Tris Pharma

AR&D Scientist I/II

Monmouth Junction, NJ · On-site

Prepares analytical method development reports, technical protocols/reports and scientific packages for internal and external useCreates and reviews ARD SOPs, as neededSafely and properly disposed of ...

Element Solutions

R&D Scientist

Piscataway, NJ · On-site

We are seeking a curious, technically capable R&D Scientist to contribute to the development and ... Methodical and detail-oriented , valuing accuracy and reproducibility. * Collaborative , enjoying ...

Element Solutions Inc

R&D Scientist

Piscataway, NJ

We are seeking a curious, technically capable R&D Scientist to contribute to the development and ... Methodical and detail‑oriented , valuing accuracy and reproducibility. * Collaborative , enjoying ...

Legend Biotech USA, Inc.

Legend Biotech is seeking a Scientist I, Analytical Development as part of the Research and ... Author and review methods, protocols, and reports.Maintain reagent inventory and order materials as ...

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All JobsMethod Development Scientist JobsMethod Development Scientist Jobs in New Jersey

Method Development Scientist information

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$20

$39

$62

How much do method development scientist jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for method development scientist in New Jersey is $39.25, according to ZipRecruiter salary data. Most workers in this role earn between $28.80 and $46.88 per hour, depending on experience, location, and employer.

What is a method development scientist?

Method Development Scientists are professionals who design, develop, and validate analytical methods used to test and measure chemical, biological, or physical properties in various samples. They work primarily in laboratories within industries such as pharmaceuticals, biotechnology, and environmental science. Their role ensures that testing methods are accurate, reliable, and compliant with regulatory standards, which is crucial for product development, quality control, and safety assessment.

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

To thrive as a Method Development Scientist, you need a solid background in analytical chemistry, experience with experimental design, and at least a bachelor's or master's degree in chemistry or a related field. Expertise with analytical instrumentation such as HPLC, GC, and mass spectrometry, as well as familiarity with regulatory guidelines and data analysis software, is typically required. Strong problem-solving skills, attention to detail, and effective communication help you excel when troubleshooting and collaborating with cross-functional teams. These skills and qualifications are crucial for developing robust, reliable methods that support quality control, regulatory compliance, and innovation in scientific research.

What are some typical challenges a method development scientist might encounter during the development of new analytical methods?

A Method Development Scientist often faces challenges such as optimizing analytical procedures for sensitivity and specificity, troubleshooting instrument or sample issues, and ensuring methods are robust enough for routine use. Balancing regulatory compliance with innovative approaches can also be demanding, especially when adapting methods to complex or novel sample matrices. Collaboration with cross-functional teams, such as QC, R&D, and regulatory affairs, is key to overcoming these challenges and ensuring successful method validation and transfer.

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

AspectMethod Development ScientistAnalytical Chemist
Primary FocusDesigning and optimizing new analytical methodsPerforming routine analysis and testing
Work EnvironmentResearch labs, product developmentQuality control labs, manufacturing support
Required CredentialsBachelor's or Master's in Chemistry or related fieldBachelor's or Master's in Chemistry or related field
Industry UsagePharmaceuticals, biotech, chemicalsPharmaceuticals, food, cosmetics

While both roles require a background in chemistry and similar credentials, a Method Development Scientist focuses on creating and refining new analytical methods, often in research and development settings. An Analytical Chemist typically performs routine testing and analysis to ensure product quality. The roles are complementary but differ mainly in scope and focus within the industry.

What does a method development scientist do?

A method development scientist designs, optimizes, and validates laboratory procedures to ensure accurate and reliable analytical testing. They often work with techniques such as chromatography or spectroscopy and use specialized software, following regulatory guidelines to develop new methods or improve existing ones. Their work supports quality control, research, and regulatory compliance in industries like pharmaceuticals and biotech.

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

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

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

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

Method Development Scientist jobs near you
Infographic showing various Method Development Scientist job openings in New Jersey as of August 2026, with employment types broken down into 60% Full Time, and 40% Contract. Highlights an 100% In-person job distribution, with an average salary of $81,645 per year, or $39.3 per hour.

Scientist, Analytical Method Development - Radiopharmaceuticals

Sk Life Science, Inc.

Paramus, NJ • On-site

Full-time

Re-posted 19 days ago

Job description

Overview
The Scientist, Analytical Method Development for Radiopharmaceuticals, is responsible for the development, optimization, validation, and transfer of analytical methods supporting radiopharmaceutical products across early- and late-stage development. This role requires strong technical expertise in analytical chemistry and a solid understanding of the unique challenges associated with radiopharmaceuticals, including short half-life materials, radioactive impurities, and time-critical testing. The position sits within CMC organization and works closely with Quality, Manufacturing, and external partners to ensure robust, compliant, and transferable analytical methods.
Responsibilities
Analytical Method Development
  • Working with CDMOs, develop, optimize, and qualify analytical methods to support radiopharmaceutical drug substance and drug product development
  • Design methods suitable for radioactive materials, accounting for decay, sensitivity, speed, and radiation safety considerations
  • Apply a range of analytical techniques, including but not limited to HPLC/UPLC, radio-HPLC, GC, TLC, radio-TLC, spectroscopy, and wet chemistry methods

Method Validation & Transfer
  • Author and execute method qualification, validation, and verification protocols in accordance with ICH and regulatory expectations
  • Lead or support analytical method transfer to internal QC laboratories, CDMOs, and external testing sites
  • Troubleshoot method performance issues during transfer and routine testing, ensuring method robustness and reproducibility

Radiopharmaceutical-Specific Testing
  • Support testing of precursors and radiolabeled finished drug products, including identity, purity, potency, and impurity profiling
  • Collaborate with Radiation Safety Officers (RSO) to ensure compliant handling and testing of radioactive materials
  • Develop rapid and fit-for-purpose methods suitable for short half-life products and just-in-time manufacturing models

Documentation & Regulatory Support
  • Prepare and review technical reports, method SOPs, validation reports, and specifications
  • Contribute to CMC sections of regulatory submissions (IND, CTA, IMPD, NDA/BLA) related to analytical methods
  • Support regulatory interactions, audits, and inspections by providing analytical expertise and documentation

Cross-Functional Collaboration & Continuous Improvement
  • Partner with CMC, Process Development, Manufacturing, Quality, and Clinical teams to align analytical strategies with development timelines
  • Support investigation of OOS/OOT results and implement corrective actions as needed
  • Drive continuous improvement initiatives in analytical efficiency, data integrity, and method lifecycle management

Qualifications
Required
  • Bachelor's degree in Chemistry, Biology, Life Sciences, or a related discipline
  • Minimum of 7 years of experience in the pharmaceutical or biotechnology industry
  • 2-3 years of direct experience working with radiopharmaceutical products
  • Strong hands-on experience in analytical method development and characterization
  • Demonstrated experience with analytical method transfer to internal or external laboratories

Preferred
  • Advanced degree (Master's or Ph.D.) in Chemistry, Pharmaceutical Sciences, or a related field
  • Experience supporting regulatory submissions involving radiopharmaceuticals
  • Familiarity with GMP environments and data integrity requirements (e.g., ALCOA+)

Key Competencies
  • Strong analytical and problem-solving skills with attention to detail
  • Ability to work effectively in fast-paced, time-sensitive environments
  • Excellent technical writing and documentation skills
  • Strong collaboration and communication skills across cross-functional teams
  • Commitment to quality, compliance, and scientific rigor

Apply