LCMS Bioanalytical Scientist I at Pharmaron
Germantown, MD 20876, USA -
Full Time


Start Date

Immediate

Expiry Date

29 Oct, 25

Salary

80000.0

Posted On

30 Jul, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Position: LCMS Bioanalytical Scientist I
FLSA Status: Exempt
Salary Range: $80k - $100k
Location: Germantown, MD

JOB OVERVIEW:

Pharmaron Germantown is seeking an LCMS Bioanalytical Scientist I to join our fast-paced, collaborative bioanalytical team. In this role, you’ll support LC-MS/MS method development, validation, and sample analysis activities that directly contribute to advancing clinical and preclinical research.
This is an exciting opportunity for a driven scientist who thrives in a dynamic, growth-oriented environment and is looking to make an impact in the drug development process.

Responsibilities
  • Collaborates with the lead scientist in overseeing the execution of LC-MS/MS assay development, validation, and sample analysis activities.
  • Generates, reviews, and interprets data using Laboratory Information Management Systems (Watson) in alignment with FDA and ICH bioanalytical method validation guidance.
  • Responsible for training binder self-review and completion of initial and refresher trainings as required by Pharmaron (Germantown) Lab Services Inc SOP.
  • Contributes to the training, mentoring, and performance monitoring of junior staff.
  • May serve as line manager for Associate Bioanalytical Scientists.
  • Acts as responsible person for scheduling, maintenance, and calibration of laboratory equipment, ensuring operational excellence.
  • Leads and/or participates in department-initiated process improvements, as required.
  • Prepares or reviews standard operating procedures for use by the company, ensuring they meet GLP/GCP and FDA requirements.
  • Always complies with the Laboratory Safety Policy and company SOPs unless otherwise defined in study-specific plans.
  • Provides support in sourcing project-specific consumables, reference materials, and control plasma.
  • Participates in preclinical and clinical data management, including data transfers and QA audit response support.
  • Assists with onboarding activities and initial training of new hires.
Loading...