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Lab Scientist

Job in Hazelwood, Haywood County, North Carolina, 28738, USA
Listing for: Stellar IT Solutions LLC
Full Time position
Listed on 2026-08-03
Job specializations:
  • Quality Assurance - QA/QC
  • Research/Development
    Lab Tech / Assistant, Pharmaceutical Science/ Research, Biotech Research
Salary/Wage Range or Industry Benchmark: 85000 - 110000 USD Yearly USD 85000.00 110000.00 YEAR
Job Description & How to Apply Below
Location: Hazelwood

Lab Scientist – Analytical Chemistry, Technical Operations

Duration: 6+ Month Contract

Position Summary

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.

Key Responsibilities Analytical Laboratory

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.

Documentation & Quality Systems

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.

Laboratory Operations

Coordinate laboratory logistics to support testing schedules and project timelines.

Follow and promote laboratory safety procedures.

Support continuous improvement initiatives across laboratory operations.

Required Qualifications

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.

Preferred Qualifications

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.

Working Conditions

Regular handling of chemicals, reagents, and analytical instrumentation.

Ability to stand, walk, and perform routine laboratory tasks for extended periods.

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