Job Summary Quasar Instruments is seeking a motivated Validation & Applications Chemist for a fulltime, in-person position to support validation implementation, training, and laboratory R D. This role is ideal for an individual who enjoys both customer interaction and hands-on analytical laboratory work, including analytical method development, validation, troubleshooting, and experimental research using mass spectrometry and other analytical instrumentation (e.g., LC-MS/MS, GC-MS, ICP-MS, QTOF, and related platforms Primary Responsibilities (60-70%)
- Customer Applications & Validation Secondary Responsibilities (20-30%)
- In-House Laboratory Support & R D Support Growth & Advanced Responsibilities (10-20%)
- Method Development The ideal candidate for this position is highly adaptable and able to thrive in dynamic laboratory and customer environments.
Because client validation and onsite support can change rapidly, this role requires someone who is flexible, solutions-oriented, and comfortable adjusting priorities in real time. This position requires approximately 30-40% travel, including customer site visits lasting approximately 1-2 weeks at a time. Duties/Responsibilities Travel approximately 30-40% to customer laboratory sites to provide hands-on customer training and perform validation experiments. Work directly with client laboratory personnel to coordinate and execute validation studies, troubleshoot instrument and laboratory workflow issues, and guide customers through the validation process from initiation through successful completion. Prepare reagents, stock solutions, calibrators, controls, troubleshooting samples and other materials required for validation and research activities. Accurately document validation studies, experiments, training activities, and laboratory records in accordance with company procedures. When not traveling, support internal team operations by assisting with validation activities, data review, troubleshooting, assay optimization, workflow improvements, and other research and development initiatives. Prepare stock solutions, calibrators & controls, and other laboratory materials to support client validation studies, off-site and on-site implementations, and field applications activities. Generate technical reports, validation documentation, and internal project updates. As competency is demonstrated, responsibilities will expand to include the method development on mass spec-based instrumentation. Perform other duties as assigned. Required Skills/Abilities Excellent verbal and written communication skills with a strong customer-focused and professional mindset Strong organizational, analytical, and problem-solving skills with attention to detail Ability to adapt quickly and pivot in changing customer, laboratory, and project environments Ability to manage multiple projects, priorities, and deadlines in a fast-paced environment Ability to think critically, work outside traditional approaches, and confidently handle situations with limited direction Ability to learn new workflows, systems, instrumentation, and processes quickly Ability to work independently at customer sites with minimal supervision while collaborating effectively across departments Ability to remain calm, flexible, and productive under pressure Strong initiative, accountability, and willingness to take ownership of challenges through resolution Flexibility with travel schedules, including changing travel dates, extended onsite support, and overnight travel as business needs require Proficiency with Microsoft Office Suite or related software Education and Experience Bachelor's degree in chemistry, biology, or related scientific field required Minimum of 1 year of hands-on LCMS, GCMS, or other mass spectrometry experience, with theoretical knowledge of mass spectrometry, analytical chemistry, or clinical urine toxicology. Experience working in a laboratory environment with strong attention to quality, compliance, and documentation practices Demonstrated proficiency with standard laboratory equipment, reagents, and laboratory safety practices, including pipettes, centrifuges, PPE, SDS documentation, and handling of organic and aqueous materials Preferred Experience with Agilent or other analytical instrumentation platforms (e.g., LC-MS/MS, GC-MS, ICP-MS, QTOF, HPLC, GC), including method optimization, data review, and troubleshooting. Experience supporting or performing analytical method validations in clinical, environmental, forensic, pharmaceutical, research, or other regulated laboratory environments. Experience with quality systems or regulatory requirements, such as
COLA, CLIA, CAP, ISO
17025 or Laboratory Developed Tests (LDTs), is preferred. Previous customer-facing, onsite laboratory support, technical training, applications, or field service/field applications experience.
Job Type:
Full-time Pay:
$55,000.00
00 per year
Benefits:
Dental insurance Employee assistance program Health insurance Health savings account Life insurance Paid time off Retirement plan Vision insurance
Education:
Bachelor's (Preferred)
Experience:
Microsoft Office:
1 year (Required) Time management: 1 year (Required) Analysis skills: 1 year (Required) Ability to
Commute:
Colorado Springs, CO 80919 (Preferred) Ability to
Relocate:
Colorado Springs, CO 80919: Relocate before starting work (Preferred) Willingness to travel: 25% (Required)
Work Location:
In person
