Scientist; Stability & References
Listed on 2026-08-24
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Scientist (Stability & References)
Scientist for a long-term engagement at one of our Global consumer products clients in Summit NJ. The role is eligible for medical benefits, paid time off including vacation (PTO), and holidays, 401K, and annual performance reviews.
Schedule:
Monday-Friday, Day Shift Compensation: $35-50 an hour Note :
This site is BYOD and candidates are required to supply their own laptop
The Stability Testing & Reference Standards Laboratory Specialist is responsible for supporting the planning, execution, documentation, review, and data management activities associated with stability testing and reference standard programs. This role provides laboratory and LIMS support to ensure stability samples and reference standards are tested according to approved protocols, methods, specifications, schedules, and applicable GMP requirements.
The position will work closely with Quality, Laboratory, Stability, and other cross-functional stakeholders to ensure timely and compliant execution of testing activities, accurate laboratory documentation, appropriate investigation of laboratory events, and reliable data trending.
The individual will be expected to operate in a highly regulated laboratory environment and demonstrate strong attention to detail, sound analytical judgment, data integrity awareness, and adherence to laboratory safety requirements.
Key Responsibilities- Stability & Reference Standard Test Scheduling
- Stability Sample Pulls & Chamber Management
- LIMS Responsibilities
- Analytical Testing
- Laboratory Notebook & Chromatography Review
- LIMS Verification, Approval & Data Trending
- Laboratory Investigation Reports (LIR)
- GMP Documentation & Data Integrity
- Laboratory Safety
- Cross-Functional Collaboration
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Chemical Engineering, or a related scientific discipline.
- Equivalent combination of education and relevant laboratory experience may be considered where permitted.
- 3-7+ years of experience in a pharmaceutical, biotechnology, consumer health, or other regulated laboratory environment, depending on level of assignment.
- Hands-on experience with analytical laboratory testing in a GMP environment.
- Experience with stability testing and/or reference standard programs strongly preferred.
- Experience working with LIMS or comparable laboratory informatics systems.
- Experience reviewing analytical laboratory documentation and chromatographic data.
- Experience with laboratory investigations, deviations, OOS/OOT assessments, or similar quality events preferred.
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