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Stellar IT Solutions LLC seeks a detail‑oriented Lab Scientist to support analytical chemistry testing and facility activities onsite. You will operate HPLC, LC‑MS, GC, spectroscopy, and Karl Fischer titration, perform method development, and ensure data integrity and safety.
The role emphasizes documentation, controlled document management, and collaboration within the Technical Operations team to meet project timelines and quality standards.
Lab Scientist – Analytical Chemistry, Technical Operations
Duration: 6+ Month Contract
We are seeking a detail‑oriented and highly organized Lab Scientist to join our Technical Operations team. This onsite role will support analytical chemistry laboratory testing and facility activities, including instrumentation operation, sample management, controlled documentation, and laboratory maintenance. The ideal candidate will bring strong analytical chemistry expertise, hands‑on experience with laboratory instrumentation, and a commitment to data integrity, safety, and continuous improvement.
Operate and maintain analytical instrumentation (HPLC, LC‑MS, GC, spectroscopy, Karl Fischer titration).
Perform routine analyses, method development, and validation activities.
Troubleshoot instrument and laboratory issues; coordinate maintenance as needed.
Draft, review, and maintain controlled documents (SOPs, analytical methods, forms, work instructions).
Ensure accurate, compliant documentation aligned with quality standards.
Manage laboratory record retention, filing, storage, and archival activities.
Coordinate laboratory logistics to support testing schedules and project timelines.
Follow and promote laboratory safety procedures.
Support continuous improvement initiatives across laboratory operations.
Bachelor’s degree in Chemistry or related scientific discipline.
3–5 years of laboratory or technical operations experience in an analytical environment.
Hands‑on experience with analytical techniques and instrumentation (HPLC, LC‑MS, GC, spectroscopy, Karl Fischer titration).
Strong knowledge of laboratory documentation practices and controlled‑document management.
Experience in pharmaceutical, biotechnology, or regulated laboratory environments.
Knowledge of GMP and data integrity principles.
Experience authoring and maintaining SOPs and quality records.
Strong written and verbal communication skills.
Excellent organizational and time‑management abilities.
Ability to work independently and collaboratively in a team environment.
High attention to detail and accuracy.
Strong problem‑solving skills with a proactive approach.
Commitment to following procedures, quality requirements, and safety standards.
Regular handling of chemicals, reagents, and analytical instrumentation.
Ability to stand, walk, and perform routine laboratory tasks for extended periods.