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Analytical Method Development Scientist Jobs (NOW HIRING)

Medix

Analytical Scientist

Cranbury, NJ · On-site

$40 - $48/hr

Senior Analytical Scientist - Method Development & Validation (CDMO) Location: Cranbury, NJ (100% Onsite) Position Type: Full-Time, Monday - Friday (9:00 AM - 5:00 PM) Compensation: $40.00 - $48.00 ...

Loyal

Principal Scientist, CMC Analytical

Success requires deep expertise in analytical method development and validation, strong data ... Serve as the technical lead and final scientific authority during OOS, OOT, and atypical result ...

New

Altasciences

Senior Analytical Scientist

Harleysville, PA · On-site

$88K - $120K/yr

Lead the development, qualification, validation, and transfer of robust analytical methods ... Evaluate scientific data to draw clear conclusions, guide future work, and communicate findings ...

DISCGENICS INC

Analytical Scientist

Salt Lake City, UT · On-site

The Scientist/Senior Scientist, Analytical Sciences is responsible for the development, optimization, qualification, validation, and execution of analytical methods supporting raw materials, in ...

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

As of Jul 17, 2026, the average hourly pay for analytical method development scientist in the United States is $42.08, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $48.56 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, and why are they important?

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.

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Analytical Method Development Scientist jobs near you
Infographic showing various Analytical Method Development Scientist job openings in the United States as of July 2026, with employment types broken down into 1% Internship, 92% Full Time, 5% Part Time, and 2% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $87,519 per year, or $42.1 per hour.
Senior Scientist, Analytical Sciences

Senior Scientist, Analytical Sciences

AstraZeneca

Santa Monica, CA • On-site

$112K - $168K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

18th of 74 rated pharmaceutical

Job description

We are seeking a collaborative and technical Senior Scientist experienced in cell culture, immunological techniques, multi-parametric flow cytometry and cell-based functional assays as part of bioassay development. The individual will deliver new/optimized analytical methods and evaluate new analytical technologies. The candidate will be responsible to develop cell-based analytical methods aligned with vector and cellular therapy product CQAs to enable process development, product characterization, stability and release testing of novel engineered cell therapy products. The Senior Scientist will work extensively with the Process Development and Quality Control teams. This role is based out of Santa Monica, CA and reports directly to the Director, Product Analytical Sciences.
Responsibilities
  • Provide strategic, technical, and scientific leadership to a highly technical analytical method development team, assign duties, review data, and reinforce regulatory concepts (cGMP).
  • Responsible to advance and implement cell-based bioassay/potency (e.g. cytotoxicity, proliferation, cytokine production) and immunophenotyping by multi-parametric flow cytometry methods from conception through optimization, qualification, and method transfer to Quality Control and/or external partners as part of an analytical control strategy and in support of Process Development.
  • Employ quality by design (QbD) and design of experiment (DOE) approaches to method development to quickly identify robust operating regions within phase-appropriate pre-defined acceptance criteria aimed to meet ICH guidelines.
  • Work with Process Development, executing and documenting analytical methods as part of experimental study plans to progress and characterize novel engineered cell therapy platforms, and occasionally perform routine assays for characterization.
  • Work cross-functionally with Quality partners during technology transfers, assist in drafting qualification/validation protocols/reports.
  • Write, review and edit accurate technical and development reports, CMC sections for regulatory submissions, and SOP/maintenance/user requirements for relevant equipment
  • Participate in group and department meetings, present scientific data, provide expertise in areas of responsibility.
  • Maintain, calibrate and operate analytical equipment and instrumentation that is used routinely in execution of assays.

Required Qualifications and Skills
  • BS/BA in Immunology, Cell Biology, Bioengineering, Analytical Sciences, or a related discipline with 5+ years of relevant hands-on experience or MS/MA with 3+ years of relevant experience or Ph.D. with no prior industry experience
  • Demonstrate knowledge of Process Development of cellular therapy products and Analytical Method Development within a regulated environment
  • First-hand experience in development and qualification of immunoassays, multi-parameter flow cytometry, and cell-based potency methods for release in a QC/regulated environment
  • Demonstrate advanced knowledge in T cell biology and cell signaling pathways
  • Excellent skills in Microsoft Excel, Word and PowerPoint and data analysis software (e.g. Prism, JMP, FlowJo, CytEpert, SoftMax Pro)
  • Ability to think critically and demonstrate troubleshooting and problem-solving skills.
  • Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description.
  • Experience and aptitude in working in a fast-paced laboratory environment with moderate direction and supervision.

Preferred skills
  • Extensive hands-on experience in executing assays and analyzing data using multi-color flow cytometry (10+ colors).
  • Demonstrate knowledge of QbD approaches to analytical method development including gap and risk assessments, DOE and statistical analysis.

#CellTherapy
The annual base pay for this position ranges from $112K to $168K. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
10-Jul-2026
Closing Date
19-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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