Sr. Bioanalytical Chemist

Battelle; Columbus (OH); On-site; USD 82,000 - 116,000; Full time

Benefits offered by this job

Compressed work schedule

Hybrid work arrangement

Paid time off (PTO)

Medical, dental, and vision coverage

401(k) retirement plan

Job summary

Battelle is seeking a Bioanalytical Chemist III to design and execute complex analytical studies, develop and validate bioanalytical methods, and communicate findings to clients and project teams. The role supports discovery, safety, and efficacy programs, with 80% onsite presence at Columbus, OH and West Jefferson, OH locations.

The team operates under GLP/SOP frameworks, emphasizes data quality and regulatory compliance, and offers a hybrid work option while maintaining a strong emphasis on

Qualifications

• Bachelor’s degree with 5 years of experience or master’s degree with 2 years or PhD in related field.
• Experience with chromatographic systems coupled to mass spectrometry (LC-MS and/or GC-MS).
• Experience operating, maintaining, calibrating, and troubleshooting advanced MS instrumentation.
• Strong experience in quantitative chemical analysis and bioanalytical method development and validation.
• Excellent analytical and technical reporting skills.

Responsibilities

• Develop, validate, optimize, and apply bioanalytical methods for exploratory, nonclinical, and regulated studies.
• Perform qualitative and quantitative analyses of biological, organic, and inorganic samples using LC-MS/MS, GC-MS and related instrumentation.
• Prepare protocols, study plans, technical reports, and documentation conveying procedures and results.
• Engage with clients to understand technical needs and discuss results and next steps.
• Lead or support research projects, coordinating activities to meet scope, budget, and schedule.

Skills

Quantitative analysis

Bioanalytical methods development

Data interpretation

Analytical problem solving

Education

Bachelor’s degree in related field

Master’s degree in related field

PhD in related field

Tools

LC-MS/MS

GC-MS

Shimadzu

SCIEX

Agilent

MassHunter

Job description

Job Summary

Join our team as a Bioanalytical Chemist III and play a key role in delivering high-quality scientific solutions that support research, development, and regulatory programs. In this role, you will design and execute complex analytical studies, develop and validate bioanalytical methods, solve technical challenges, and communicate scientific findings to clients and project teams. The Life Sciences Research team provides fast, accurate answers for discovery, safety and efficacy with our world-class facilities and ability to meet unique technical, development and regulatory needs for our clients. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. This position is 80% onsite with time at both our Columbus, OH and West Jefferson, OH locations.

Responsibilities

• Develop, validate, optimize, and apply bioanalytical methods to support exploratory, nonclinical, and regulated studies.


• Perform qualitative and quantitative analyses of biological, organic, and inorganic samples using advanced analytical techniques.


• Conduct sample preparation, extraction, cleanup, and analysis using LC-MS/MS, GC-MS, and related instrumentation.


• Apply knowledge of analyte behavior, metabolism, and biotransformation to method development and data interpretation.


• Analyze and interpret complex analytical data to generate accurate, reliable, and scientifically defensible results.


• Establish appropriate acceptance criteria and perform technical data reviews.


• Draw conclusions, troubleshoot analytical challenges, and recommend solutions to improve study outcomes and laboratory efficiency.


• Troubleshoot instruments and methods, document investigations, and implement corrective actions.


• Ensure data quality, accuracy, and compliance with project requirements and quality objectives.


• Prepare protocols, methods, study plans, technical reports, and other documentation that clearly conveys procedures, results, and conclusions.


• Engage directly with clients to understand technical needs, share project updates, discuss results, and recommend next steps.


• Lead or support research and technical projects, coordinating activities to meet scope, budget, and schedule requirements.


• Collaborate with scientists, project managers, quality personnel, regulatory teams, and clients to achieve project objectives.


• Maintain effective communication with clients and participate in technical discussions and project reviews.


• Identify and evaluate emerging technologies, analytical approaches, and laboratory capabilities that support business growth and innovation.


• Prepare, review, and maintain technical reports, study records, and scientific documentation.


• Ensure compliance with GLP requirements, SOPs, laboratory quality standards, and applicable regulatory guidelines.


• Maintain accurate, complete laboratory records and follow applicable quality systems, safety requirements, and standard operating procedures.


• Follow all laboratory safety procedures and requirements when working with hazardous materials and biological samples.


• Provide technical guidance, training, and mentorship to junior scientists and laboratory staff.


• Support proposal development through technical contributions, scope development, and project estimates.


• Present scientific findings to clients, project teams, and professional audiences through reports and presentations.

Key Qualifications

• Bachelor’s degree in related fields with 5 years of experience or master’s degree in related field with 2 years of experience or PhD; or an equivalent combination of education and or experience in a related field.


• Demonstrated experience with chromatographic systems coupled to mass spectrometry, including LC-MS and/or GC-MS platforms.


• Experience operating, maintaining, calibrating, and troubleshooting advanced mass spectrometry instrumentation.


• Strong experience in quantitative chemical analysis and bioanalytical method development and validation.


• Excellent analytical, problem-solving, written communication, and technical reporting skills.


• Ability to analyze complex datasets, identify trends, and resolve technical issues.


• Effective verbal communication and interpersonal skills, with the ability to interact professionally with clients and colleagues.


• Ability to manage multiple priorities, work independently, and contribute effectively in a team environment


• U.S. citizenship and/or U.S. person status as required for project and export control requirements.


• Ability to work in a BSL-2 laboratory environment and wear required personal protective equipment.


• Willingness to participate in medical screening and random drug testing programs as required.

Preferred Qualifications

• Experience working in GLP or other regulated laboratory environments.


• Knowledge of GLP, ISO, EPA, FDA, or related regulatory requirements.


• Experience with Shimadzu, SCIEX, or Agilent analytical instrumentation.


• Experience using Watson™, MassHunter™, or similar analytical software platforms.


• Knowledge of metabolism, biotransformation, pharmacokinetics, or related biological processes.


• Experience supporting client-sponsored research, contract research, or government-funded programs.


• Experience leading technical discussions or serving as a scientific point of contact for clients.

Compensation Data

Battelle is committed to fair and equitable compensation practices. The salary range for this role is $81,600 - $116,300, in addition to our comprehensive benefits package. A candidate’s salary is determined by various factors, including but not limited to education, relevant work experience, skills, and certifications. Salary ranges may vary based on geographic location and market conditions.

Benefits: Live an Extraordinary Life

• Balance life through a compressed work schedule: Most of our team follows a flexible, compressed work schedule that allows for every other Friday off - giving you a dedicated day to accomplish things in your personal life without using vacation time.


• Enjoy enhanced work flexibility, including a hybrid arrangement: You have options for where and when you work. Our Together with Flexibility model allows you to work 60% in-office and 40% remote, with Monday and Tuesday as common in-office days, dependent on team and position needs.


• Take time to recharge: You get paid time off to support work-life balance and keep motivated.


• Prioritize wellness: Stay healthy with medical, dental, and vision coverage with wellness incentives and benefits plus a variety of optional supplemental benefits.


• Better together: Coverage for partners, gender-affirming care and health support, and family formation support.


• Build your financial future: Build financial stability with an industry-leading 401(k) retirement savings plan. For most employees, we put in 5 percent whether you contribute or not, and match your contributions on top of that.


• Advance your education: Tuition assistance is available to pursue higher education.

A Work Environment Where You Succeed

For brilliant minds in science, technology, engineering and business operations, Battelle is the place to do the greatest good by solving humanity’s most pressing challenges and creating a safer, healthier and more secure world.

You will have the opportunity to thrive in a culture that inspires you to:

• Apply your talent to challenging and meaningful projects


• Receive select funding to pursue ideas in scientific and technological discovery


• Partner with world-class experts in a collaborative environment


• Nurture and develop the next generation of scientific leaders


• Give back to and improve our communities

Vaccinations & Safety Protocols

Battelle may require employees, based on job duties, work location, and/or its clients’ requirements to follow certain safety protocols and to be vaccinated against a variety of viruses, bacteria, and diseases as a condition of employment and continued employment and to provide documentation that they are fully vaccinated. If applicable, Battelle will provide reasonable accommodations based on a qualified disability or medical condition through the Americans with Disabilities Act or the Rehabilitation Act or for a sincerely held religious belief under Title VII of the Civil Rights Act of 1964 (and related state laws).

Battelle is an equal opportunity employer. We provide employment and opportunities for advancement, compensation, training, and growth according to individual merit, without regard to race, color, religion, sex (including pregnancy), national origin, sexual orientation, gender identity or expression, marital status, age, genetic information, disability, veteran-status veteran or military status, or any other characteristic protected under applicable Federal, state, or local law. Our goal is for each staff member to have the opportunity to grow to the limits of their abilities and to achieve personal and organizational objectives. We will support positive programs for equal treatment of all staff and full utilization of all qualified employees at all levels within Battelle.

The above statements are intended to describe the nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, activities and skills required of staff members. No statement herein is intended to imply any authorities to commit Battelle unless special written permission is granted by Battelle's Legal Department.

For more information about our other openings, please visit www.battelle.org/careers