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Senior Scientist I, Analytical Chemistry

Job in Lexington, Fayette County, Kentucky, 40598, USA
Listing for: Kindeva
Full Time position
Listed on 2026-08-07
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Analytical Chemist
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below

Senior Scientist I, Analytical Chemistry

Lexington, KY, USA

Job Description

Posted Wednesday 10 June 2026 at 04:00

Our Work Matters

At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.

Why Kindeva?

  • Collaborative team culture
  • Direct impact on patient care

The Impact You Will Make

Transform Lives Through Scientific Innovation

Join a growing pharmaceutical CDMO where your expertise will directly support the development of innovative drug products that improve patient health worldwide.

As a Senior Scientist, Analytical Chemistry, you will serve as a technical leader within the R&D Analytical Chemistry group, leading analytical strategies that support pharmaceutical product development from early-stage development through commercialization. You will provide scientific leadership in method development, validation, verification, transfer, and troubleshooting activities while partnering with cross-functional teams to advance customer programs and internal development initiatives.

This role is ideal for a scientist who thrives in a fast-paced development environment, enjoys solving complex technical challenges, and is passionate about mentoring others while advancing analytical capabilities within a growing organization.

Our Lexington site continues to experience significant growth across development and manufacturing programs. This position offers the opportunity to lead complex analytical projects, support innovative drug development programs, influence technical strategy, mentor junior scientists, and expand Kindeva's analytical capabilities while working closely with customers and internal development teams.

Responsibilities

Analytical Method Development & Validation

  • Lead the development, optimization, and validation of robust analytical methods for drug substances and drug products in accordance with ICH, USP, and regulatory guidelines.
  • Design and execute complex analytical studies to support formulation development, process development, stability programs, and customer projects.
  • Lead or support technology transfer of analytical methods to internal and external QC laboratories and CMOs.
  • Support qualification of new analytical laboratory equipment.
  • Implement new analytical techniques and instrumentation to expand internal capabilities.
  • Act as a subject matter expert (SME) for analytical technologies, method troubleshooting, and regulatory inspections.

Scientific Leadership & Technical Execution

  • Provide leadership and execution of complex scientific experiments.
  • Utilize creative thinking to generate solutions to complex technical problems.
  • Prioritize personal workload to ensure key objectives are achieved on time and within project expectations.
  • Stay current with advancements in analytical technologies, industry best practices, and regulatory expectations.
  • Mentor and provide technical oversight to junior scientists and analysts, ensuring scientific rigor and compliance with quality standards.

Documentation, Compliance & Regulatory Support

  • Author and review technical documents, including method validation protocols and reports, specifications, analytical development reports, and regulatory submissions (IND, NDA, ANDA, BLA).
  • Prepare and maintain accurate and timely laboratory records in accordance with company policies and regulatory requirements.
  • Ensure compliance with GMP requirements, regulatory expectations, and internal quality systems.
  • Support regulatory inspections, customer audits, and compliance initiatives as required.

Cross-Functional Collaboration & Business Support

  • Collaborate cross-functionally with Formulation Development, Process Development, Quality Assurance, Regulatory Affairs, Manufacturing, and customer teams to ensure successful product development.
  • Represent Analytical Chemistry in project meetings and customer meetings with limited supervision.
  • Contribute to continuous improvement initiatives and innovation within the analytical development function.
  • Support Marketing and Business Development activities through technical presentations, posters, publications, blogs, white papers, and industry conferences.
  • Support cross-functional training and execution of activities within the R&D Product Development & Design Team as needed.

Qualifications

  • PhD in a scientific discipline with 1+ years of relevant experience;
    Master's degree with 3+ years of experience;
    Bachelor's degree with 6+ years of experience; or 9+ years of equivalent experience without a degree.
  • In-depth experience with analytical techniques including HPLC, UPLC, GC, UV, FTIR, spray testing, compendial methods, and related analytical technologies.
  • Demonstrated success in analytical method development, optimization, validation, and troubleshooting under GMP and ICH guidelines.
  • Strong understanding of regulatory requirements and CMC components of pharmaceutical drug development.
  • Experience with stability testing, impurity/degradant characterization, and forced degradation studies.
  • Proven ability to lead technical…
Position Requirements
10+ Years work experience
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