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Senior Analytical Scientist Jobs (NOW HIRING)

Senior Analytical Chemist

Olive Branch, MS ยท On-site

$80K - $95K/yr

Senior Analytical Chemist / Quality Control Manager (Working Manager) Location: Olive Branch, MS ... Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to ...

Senior Analytical Chemist

Fishers, IN ยท On-site

$113K - $132K/yr

Senior Analytical Chemist| Req ID: 17219 | HR Contact: Elizabeth Bertapelle | Location: Building ... Data Analysis and Reporting - Interpret complex scientific data, draw relevant conclusions, and ...

Analytical Sr Scientist What you will do Let's do this! Let's change the world! In this vital role you will work closely with a team of analytical chemists, organic chemists and formulators ...

Analytical Sr Scientist What you will do Let's do this! Let's change the world! In this vital role you will work closely with a team of analytical chemists, organic chemists and formulators ...

Senior Analytical Chemist

Warrington, PA ยท On-site

$87K - $106K/yr

We believe the best scientific innovations are built through collaborations. The Senior Analytical Chemist primary responsibility is independent development of analytical methods that are suitable ...

The R&D Analytical Scientist serves as a technical resource for Eurofins Environment Testing ... Prepares reports and recommendations for senior laboratory management. * Assists with set up of and ...

... Senior Scientist. The Scientist I works primarily within liquid chromatography - including both ... Analyze chromatographic and spectroscopic data using vendor software (ChemStation, MassHunter ...

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Senior Analytical Scientist information

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$55.5K

$119.5K

$174K

How much do senior analytical scientist jobs pay per year?

As of Aug 8, 2026, the average yearly pay for senior analytical scientist in the United States is $119,503.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,500.00 and $150,000.00 per year, depending on experience, location, and employer.

What does a senior analytical scientist do?

As a Senior Analytical Scientist, you can expect to lead method development, validation, and troubleshooting activities, as well as oversee complex analytical projects from start to finish. Your daily responsibilities might include analyzing samples, interpreting data, preparing technical reports, and mentoring junior scientists. Collaboration is common with cross-functional teams such as quality assurance, product development, and manufacturing, ensuring comprehensive solutions to scientific challenges. This role requires balancing hands-on laboratory work with project management duties to deliver reliable results that support organizational goals.

What is a senior analytical scientist?

A Senior Analytical Scientist is a highly experienced professional responsible for developing, validating, and implementing analytical methods to support research, product development, and quality control. They analyze complex data, ensure compliance with regulatory standards, and troubleshoot technical issues in laboratory settings. Additionally, they often lead teams, mentor junior scientists, and collaborate with cross-functional departments to drive innovation and improve processes.

What skills and qualifications are needed to be a senior analytical scientist?

To thrive as a Senior Analytical Scientist, you need advanced knowledge in analytical chemistry, method development, and data interpretation, usually supported by a Ph.D. or master's degree in a scientific field. Familiarity with laboratory instrumentation such as HPLC, GC-MS, and validation software, along with certifications like GLP/GMP training, is highly valued. Strong problem-solving skills, attention to detail, effective communication, and leadership ability help individuals excel in team-based laboratory environments. These skills and attributes ensure accurate data analysis, method robustness, and successful project delivery in compliance-driven industries.

More about Senior Analytical Scientist jobs
What cities are hiring for Senior Analytical Scientist jobs? Cities with the most Senior Analytical Scientist job openings:
What are the most commonly searched types of Analytical Scientist jobs? The most popular types of Analytical Scientist jobs are:
What states have the most Senior Analytical Scientist jobs? States with the most job openings for Senior Analytical Scientist jobs include:
Infographic showing various Senior Analytical Scientist job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 90% Full Time, 5% Part Time, and 4% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $119,503 per year, or $57.5 per hour.

Senior Scientist, Analytical CMC

Eikon Therapeutics

Millbrae, CA โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Job description

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
Position
The Senior Scientist, CMC Analytical Lead provides analytical leadership for drug substance and drug product programs from IND-enabling studies through clinical development, registration, and commercial readiness. This role leads phase-appropriate analytical strategy across CMC activities, partnering closely with CMC, Quality, Regulatory, Supply Chain, and external CRO/CDMO organizations to ensure high-quality analytical deliverables that support program milestones and regulatory submissions. While the position includes hands-on analytical support, its primary focus is providing program-level leadership, cross-functional coordination, risk assessment, and oversight of analytical development activities. As part of a growing CMC Analytical team, this role offers the opportunity to make a meaningful impact on development programs while advancing into broader analytical leadership.
About You
You are a scientifically curious, collaborative analytical scientist with experience supporting drug substance and drug product development across the CMC lifecycle. You bring strong technical expertise in analytical method development, troubleshooting, transfer, and validation, along with a solid understanding of phase-appropriate CMC, GMP, and regulatory expectations. You excel at managing multiple priorities, translating scientific data into practical, phase-appropriate decisions, communicating complex scientific concepts to cross-functional teams, and collaborating with cross-functional stakeholders and external CRO/CDMO partners to advance analytical strategies and program deliverables.
What You'll Do
  • Serve as the CMC Analytical Lead for assigned drug substance and drug product programs, coordinating analytical activities, tracking deliverables, communicating risks, and supporting program milestones in collaboration with senior technical and cross-functional stakeholders.
  • Support analytical method development, troubleshooting, qualification, transfer, and validation for drug substance, intermediates, raw materials and drug product, as appropriate for the stage of development.
  • Provide hands-on or laboratory-facing analytical support for non-GMP sample analysis for creation of CoA, method development, troubleshooting, investigation support, data interpretation, and resolution of technical issues during development, transfer, validation, release, or stability testing.
  • Provide scientific oversight of CRO/CDMO analytical activities, including review of methods, protocols, reports, deviations, investigations, data summaries, and timelines to ensure quality, scientific soundness, and phase-appropriate execution.
  • Contribute to phase-appropriate analytical control strategies, including specifications, method readiness, reference standards, impurity control, stability strategy, shelf-life planning and stability trending, and justification of analytical approaches with guidance from senior CMC, Quality, Regulatory, and program stakeholders as appropriate.
  • Collaborate with Research, Drug Substance, Drug Product, Regulatory Affairs, Quality Assurance, Manufacturing, Supply Chain, and Clinical Operations to ensure analytical deliverables support development, clinical supply, regulatory filings, and program decision-making.
  • Author, review, and contribute to analytical technical documents and regulatory submission content, including development reports, qualification or validation protocols and reports, specifications, stability summaries, shelf-life assessments, INDs, IMPDs, NDAs, and responses to regulatory questions.
  • Proactively identify analytical risks, propose mitigation strategies, communicate recommendations clearly, and provide technical guidance to junior staff or external collaborators as appropriate.

Qualifications
  • Degree in analytical chemistry, chemistry, pharmaceutical sciences, or a related discipline, with typical overall experience of Ph.D. 5+ years, M.S. 14+ years, or B.S. 16+ years, including directly relevant experience in analytical development, or CMC analytical support for clinical and/or commercialization stages; 5-6+ years of directly relevant experience is expected for M.S.-level candidates and 10+ years for B.S.-level candidates. Equivalent combinations of education and relevant experience may be considered.
  • Experience supporting DS and/or DP analytical development from clinical through registration.
  • Working knowledge of key analytical techniques, including HPLC/UPLC, dissolution, GC, LC-MS, KF, spectroscopy, solid-state, and compendial methods.
  • Hands-on experience with method development, troubleshooting, qualification, transfer, and/or validation in pharmaceutical or regulated lab settings.
  • Understanding of phase-appropriate CMC, GMP/non-GMP, quality, and regulatory expectations for methods, validation, impurities, stability, shelf-life, and specifications.
  • Strong communication, collaboration, organization, and problem-solving skills, with ability to manage priorities and explain scientific rationale clearly.
  • Experience representing analytical development on cross-functional CMC teams from IND-enabling through later-stage development highly preferred.
  • Experience with analytical control strategy, specifications, stability, shelf-life, trending, or regulatory submission content highly preferred.
  • Experience overseeing CRO/CDMO or external lab activities highly preferred.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
  • 401k plan with company matching
  • Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
  • Mental health and wellness benefits
  • Weeklong summer and winter holiday shutdowns
  • Generous paid time off and holiday policies
  • Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
  • Enhanced parental leave benefit
  • Daily subsidized lunch program when on-site

The expected salary range for this role is $154,000 to $185,850 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.