SPS Careers

Make an impact. Build a career. At Pace®, we’re committed to continuously moving science forward; to innovate and advance sustainable practices that improve the health and safety of our communities and lives. Ask any of us, and you’ll hear the same thing repeated again and again: we work here because what we do positively impacts the world.   If you’re curious, driven and inspired by the idea of doing important work with real-world impact, there’s no better place to build your career.   Find your place at Pace® Join us as a CMC Regulatory Affairs Specialist, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®.   The CMC Specialist will utilize their experience to assist in the preparation and review of documents for submission to the FDA, including formal FDA meeting requests and briefing packages, CMC components of investigational new drug (IND) applications, related progress reports, and amendments, and expedited approval programs. The CMC specialist will also perform regulatory strategy and gap analyses of clients’ materials to assess their needs as they move their drug through clinical development to marketing approval. The CMC specialist is expected to provide detailed feedback and advice into applications where clients have gaps or questions in their CMC methodology which may result in a clinical hold from the reviewing agency.   Note: Postion is Remote Note: This is an evergreen posting for future positions with Pace. If you would like to be considered during the next round of hirings and have the qualifications, please apply.

Make an impact. Build a career. At Pace®, we’re committed to continuously moving science forward; to innovate and advance sustainable practices that improve the health and safety of our communities and lives. Ask any of us, and you’ll hear the same thing repeated again and again: we work here because what we do positively impacts the world.   If you’re curious, driven and inspired by the idea of doing important work with real-world impact, there’s no better place to build your career.   Find your place at Pace® Join us as a Computer Systems Validation Specialist, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®.   This individual will support computer system validation functions on client projects.  Apply expertise cross functionally when required and demonstrates transferrable knowledge of computer system validation concepts.    Note: This is an evergreen posting for future positions within our team.  If you would like to be considered during the next round of hirings and have the qualifications, please apply

Here at Pace, our Technical Field Services (TFS) provides unique opportunities for your career to flourish. By working in diverse settings, building strong customer partnerships, and exceeding their needs. TFS team members are constantly learning and improving our processes. With over 40 years of lab operations experience, we serve a range of industries, instruments, and facilities nationwide -- meaning our team has unparalleled access to a plethora of shared knowledge powered by supportive leadership. If you're looking for a close-knit team of analytical thinkers and a dynamic, hands-on work experience, look no further. Apply to learn more about the various departments, current open positions, and competitive benefits including bonus incentives.   Here are some of our service departments within TFS!   Analytical Equipment Services   Working in our Analytical Equipment Services team allows chemists to perform hands-on work and interact directly with our clients. We specialize in servicing instrumentation such as GC, GC/MS, LC, LC/MS, IC, and Dissolution. While the instrumentation is complex, TFS has an extensive training program for new employees, as well as ongoing training to maintain the capabilities of our service staff.   Facility Qualification Services   The Facility Qualification Services (FQS) team offers exciting opportunities to perform qualification services and cleanroom certification testing in a variety of industries including medical device, life science, pharmaceuticals, defense, and other high-tech industries. No degree is needed for these roles and this team provides a unique training program that includes an escalating pay scale as you continue to learn about the industry. Opportunities for project bonus incentives!   Metrology Services   The Metrology team works in many different industries performing calibrations on lab equipment such as thermometers, centrifuges, and balances.     Different positions within TFS:   - Analytical Instrument Specialist - Cleanroom Certification Technician - Calibration Technician - Senior Facility Qualification Technician  TFS Locations - Minneapolis, MN - Houston, TX - Salem, NH - Mount Juliet, TN - Indianpolis, IN - Chicago, IL - Philidelphia, PA   Apply using this position today for a chance at exponential growth and a like-minded community invested in your success within TFS.         

Supports clients GxP Document Control function for all departments within research and development and manufacturing operations.   Note: This is an evergreen posting for future positions within our team.  If you would like to be considered during the next round of hirings and have the qualifications, please apply.

This individual will support the validation functions on client projects.  Apply expertise cross functionally when required and demonstrates transferrable knowledge of validation concepts.    Note: This is an evergreen posting for future positions within our team.  If you would like to be considered during the next round of hirings and have the qualifications, please apply.

Candidate will aid in the design, preparation, implementation, and management of client quality systems. Review of existing systems, document review, general consulting and auditing for programs needed to comply with regulatory requirements of FDA and other regulatory authorities worldwide.   Note: This is an evergreen posting for future positions within our team.  If you would like to be considered during the next round of hirings and have the qualifications, please apply.