PLS Scientist - BioPharma
Listed on 2026-07-01
-
Pharmaceutical
Pharmaceutical Science/ Research, Drug Discovery -
Research/Development
Pharmaceutical Science/ Research, Research Scientist, Drug Discovery, Biotech Research
Location: Saint Paul
Senior Scientist / Scientist 3
Shift: Monday through Friday, 8:30 AM - 5:00 PM
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.
This is a full-time, onsite, Senior Scientist / Scientist 3 position located in Oakdale, MN, Monday through Friday, 8:30 a.m.
- 5:00 p.m.
Compensation: $80,000 - $90,000 per year
The salary for this position reflects a variety of factors. Compensation will be determined based on the candidate's geographic location, relevant experience, education, skills, and alignment with internal equity. Market conditions, budgetary considerations, and organizational compensation guidelines may also influence the final offer.
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.
Job SummaryThe Scientist III / Senior Scientist will lead the design, optimization, and validation of analytical methods that support product development, regulatory submissions, and commercial readiness for biopharmaceuticals in a GMP environment.
Job Responsibilities- Lead the development, optimization, and qualification/validation of analytical methods for biopharmaceutical drug substances and drug products, including peptides, oligos, proteins, mAbs, etc.
- Serve as a technical expert for bioanalytical techniques, specifically ELISA, plate-based assays, SDS-PAGE, cell-based assays, qPCR, ddPCR, Sanger Sequencing, CE, cIEF, and similar.
- Design scientifically sound method development strategies aligned with ICH Q2(R2) and evolving regulatory expectations for biologics. Stay current with evolving regulatory expectations (ICH, USP, EP) and implement best practices.
- Author and review method development reports, validation protocols, validation reports, and laboratory methods.
- Provide scientific leadership during investigations, troubleshooting, and method lifecycle management.
- Mentor and train junior scientists and contribute to building a culture of scientific excellence and continuous improvement.
- Present data to and collaborate with client organizations.
- Bachelor's degree in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline with 8-10 years of relevant laboratory experience.
- Master's Degree in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline with 4-7 years of relevant laboratory experience.
- Ph.D. in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline with 1-4 years of relevant laboratory experience.
- Demonstrated expertise in bioanalytical method development and validation for biologics.
- Strong hands-on experience with key biopharmaceutical analytical platforms
- Familiarity with GMP, ICH guidelines, and regulatory expectations for biologics
- Excellent technical writing skills and experience
- Strong communication, leadership, and project management capabilities.
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…
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).