
1001 - 5000 employees
Environmental Consulting • Pharma/Biopharmaceutical • Medical Device
Pace® Labs is a nationwide network of laboratories and professional services that provides analytical and environmental testing, life‑sciences CDMO/CRO and central laboratory services, building‑science and laboratory support, and emergency response for contamination and outbreak events. The company delivers environmental sampling and testing (air, water, soil, PFAS, Legionella, VOCs, metals, radiochemistry, etc. ), GMP analytical testing and formulation/clinical manufacturing support for pharma and biopharma, medical device testing and regulatory/compliance consulting, plus instrument, cleanroom and facility services to regulated industries.
🔥 17 minutes ago
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1001 - 5000 employees
Environmental Consulting • Pharma/Biopharmaceutical • Medical Device
Pace® Labs is a nationwide network of laboratories and professional services that provides analytical and environmental testing, life‑sciences CDMO/CRO and central laboratory services, building‑science and laboratory support, and emergency response for contamination and outbreak events. The company delivers environmental sampling and testing (air, water, soil, PFAS, Legionella, VOCs, metals, radiochemistry, etc. ), GMP analytical testing and formulation/clinical manufacturing support for pharma and biopharma, medical device testing and regulatory/compliance consulting, plus instrument, cleanroom and facility services to regulated industries.
• Provide SDS authoring and regulatory compliance support as it applies to our client’s products • Research, author, and review chemical hazard assessments, hazard profiles, product labels, safety data sheets, and other compliance support as requested • Author safety data sheets, both U.S. and international SDS experience preferred • Review/author hazard communication and other product labels • Regulatory literature/data reviews of products and raw materials • Other regulatory compliance projects as needed
• Bachelor’s degree or higher in Chemistry • 5+ years of experience in chemical regulatory, including SDS authoring • Ability to interpret global product regulatory and hazard communication concepts • Working knowledge of GHS, OSHA, Prop65, TSCA, and other applicable regulations • Consumer label experience is a plus • Independently works within specific computer systems and databases • Can manage multiple client projects, including set up, data collection, and on-time delivery of requested deliverables • Excellent written and verbal communication skills with experience working in a client facing role
• 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
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