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Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.

Scientist III, Analytical Chemistry

Pace® Life Sciences | Oakdale, MN | Full-time | Onsite | Monday-Friday, 8:00 a.m.-5:00 p.m.

Compensation: $85,000-$95,000 per year

The salary range reflects multiple factors, including geographic location, relevant experience, education, skills, internal equity, market conditions, budget considerations, and organizational compensation guidelines. Final compensation may vary based on these factors.

Scientist III, Analytical Chemistry

Join Pace® Life Sciences as a Scientist III in Oakdale, MN, and use your advanced analytical chemistry experience to support pharmaceutical development in a GxP-regulated laboratory. In this full-time, onsite role, you will perform complex laboratory testing, develop and validate analytical methods, interpret data, troubleshoot instrumentation and methods, and help deliver reliable results that support client programs from development through commercialization.

Make an Impact. Build a Career.

Pace® Life Sciences delivers a comprehensive suite of contract CMC development, CTM manufacturing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries. Operating across a network of CDMO sites, GMP analytical testing laboratories, and manufacturing support centers, we partner with clients to efficiently advance programs from early development through commercialization.

Our experienced industry experts and continued investment in state-of-the-art facilities reflect our commitment to quality, speed, and reliability. United by a shared purpose, we bring meaningful value to patients, healthcare professionals, and health businesses worldwide by delivering services that support a safer, healthier future.

What You’ll Do:

This role is primarly focused on supporting both marketed pharmaceutical products and working with clients to commercialize new drug products. 

• Perform complex analytical testing using techniques such as HPLC, UPLC, LC-MS, GC, GC-MS, UV/Vis, FTIR, spectroscopy, dissolution, and supplementary wet chemistry in accordance with SOPs and GxP requirements.

• Lead analytical method development, optimization, and validationactivities to ensure methods are suitable for intended use and compliant with regulatory requirements.

• Analyze and interpret data, troubleshoot analytical issues, and prepare clear summaries, technical reports, and documentation of experimental results.

• Document procedures, observations, results, deviations, and investigations accurately in laboratory notebooks, LIMS, and other required systems.

• Lead and facilitate OOS and OOT investigations, help identify root causes, and support corrective and preventive actions.

• Author, review, and revise test methods, validation protocols, SOPs, and related technical documents.

• Collaborate with project teams, quality partners, and laboratory colleagues to meet client expectations.

• Follow all safety requirements, GxP standards, and internal quality policies.

• Provide technical guidance, training, and mentorship to junior scientists and laboratory personnel as needed.

What You’ll Bring:

• Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field.

• 8-10 years of relevant experience in a GxP-regulated laboratory environment.

• Hands-on experience with advanced analytical techniques, including HPLC, UPLC, GC, GC-MS, and LC-MS.

• Strong application of GLP, GMP, or GxP guidances in a laboratory setting.

• Experience with analytical method development, optimization, and validation. 

• Proficiency in data analysis, chromatographic interpretation, troubleshooting, and technical report writing.

• Familiarity with LIMS and other laboratory software.

• Excellent attention to detail, problem-solving skills, and ability to manage multiple priorities and deadlines.

• Strong written and verbal communication skills with the ability to collaborate effectively in a team environment.

• Proficiency with Microsoft Office, including Word, Excel, and PowerPoint.

• Experience providing technical guidance, mentoring, training, or informal leadership is strongly preferred.

Physical and Mental Requirements:

The physical demands described here are representative of those required to successfully perform the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. This role requires mobility to work in a laboratory and office setting; use of standard office and laboratory equipment; stamina to sit for extended periods; ability to exert up to 20 pounds of force occasionally and/or up to 10 pounds frequently to lift, carry, push, pull, or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person and by phone.

Working Environment:

Responsibilities include working in both laboratory and office settings. The role may involve exposure to chemicals, fumes, gases, noxious odors, and related items which are typical of a controlled laboratory environment.

Keywords: Scientist III, Analytical Scientist, Analytical Chemistry, Pharmaceutical Sciences, Chemist, GxP, GMP, GLP, HPLC, UPLC, GC, GC-MS, LC-MS, Spectrometry, Dissolution, UV/Vis, FTIR, Method Development, Method Validation, LIMS, OOS, OOT, Life Sciences, Oakdale MN.

Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.

Benefits
When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.

Equal Opportunity Employer

Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.