Sr. Bioanalytical Chemist

Battelle • Columbus, OH

5d • $81,600 - $116,300 • Hybrid

About The Position

Battelle is hiring a Sr. Bioanalytical Chemist, identified in the job summary as Bioanalytical Chemist III, to deliver scientific solutions supporting research, development, and regulatory programs. The role designs and executes complex analytical studies, develops and validates bioanalytical methods, solves technical challenges, and communicates scientific findings to clients and project teams. The Life Sciences Research team supports discovery, safety, and efficacy work through its facilities and technical, development, and regulatory capabilities. The position is 80% onsite, with work at both the Columbus, Ohio, and West Jefferson, Ohio locations.

The chemist performs qualitative and quantitative analyses of biological, organic, and inorganic samples using advanced techniques, including LC-MS/MS and GC-MS. The position interprets complex data, maintains quality and regulatory compliance, prepares scientific documentation, collaborates with clients and internal teams, and provides technical guidance to junior staff. The role may also support project leadership, proposals, and evaluation of emerging technologies.

Battelle offers a comprehensive benefits package, a flexible compressed work schedule for most team members, and work flexibility that may include a hybrid arrangement depending on team and position needs. The posted salary range is $81,600 to $116,300.

Requirements

• Bachelor’s degree in a related field with 5 years of experience, a master’s degree in a related field with 2 years of experience, a PhD, or an equivalent combination of education and 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, including 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 and wear required personal protective equipment.
• Willingness to participate in medical screening and random drug testing programs as required.

Nice To Haves

• 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.

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 advanced analytical techniques.
• Prepare, extract, clean up, and analyze samples using LC-MS/MS, GC-MS, and related instrumentation.
• Apply knowledge of analyte behavior, metabolism, and biotransformation to method development and data interpretation.
• Analyze complex analytical data and produce accurate, reliable, scientifically defensible results.
• Establish acceptance criteria and perform technical data reviews.
• Draw conclusions, troubleshoot analytical challenges, and recommend improvements to 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 scientific documentation.
• Engage with clients to understand technical needs, share project updates, discuss results, and recommend next steps.
• Lead or support research and technical projects, coordinating work to meet scope, budget, and schedule requirements.
• Collaborate with scientists, project managers, quality personnel, regulatory teams, and clients.
• Maintain client communication and participate in technical discussions and project reviews.
• Identify and evaluate emerging technologies, analytical approaches, and laboratory capabilities.
• 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 complete laboratory records and follow quality systems, safety requirements, and standard operating procedures.
• Follow laboratory safety procedures when working with hazardous materials and biological samples.
• Provide technical guidance, training, and mentorship to junior scientists and laboratory staff.
• Support proposal development with technical contributions, scope development, and project estimates.
• Present scientific findings to clients, project teams, and professional audiences through reports and presentations.

Benefits

• Comprehensive and competitive benefits package.
• Flexible compressed work schedule for most team members, with every other Friday off.
• Enhanced work flexibility, including a hybrid arrangement depending on team and position needs.
• Paid time off.
• Medical, dental, and vision coverage with wellness incentives and benefits.
• Optional supplemental benefits.
• Coverage for partners, gender-affirming care and health support, and family formation support.
• 401(k) retirement savings plan, with a 5% employer contribution for most employees and matching contributions.
• Tuition assistance for higher education.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level