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Senior Scientist, BioAnalytical Services

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Exton (Chester County)

On-site

USD 75,000 - 115,000

Full time

22 days ago

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Job summary

An established industry player is seeking a Senior Scientist to lead bioanalytical services. This role involves validating innovative scientific methods and performing high-volume sample analyses using advanced LC-MS/MS techniques. Candidates should possess a Ph.D. or equivalent experience, with a strong foundation in analytical chemistry and excellent communication skills. Join a dynamic team where your contributions will directly impact drug development and clinical trials. This position offers a competitive salary and comprehensive benefits, including health and dental insurance, a 401(k) plan, and more. If you're passionate about scientific excellence and teamwork, this opportunity is for you.

Benefits

Health Insurance
Dental Insurance
401(k) Plan
Life Insurance

Qualifications

  • Ph.D. or Master's in relevant field with extensive lab experience.
  • Strong understanding of analytical methods and regulatory compliance.

Responsibilities

  • Validate scientific methods and run bioanalytical assays.
  • Manage multiple projects and ensure regulatory compliance.
  • Train and mentor junior staff in GLP regulations.

Skills

Experimental Design
Data Analysis Software
Communication Skills
Team Collaboration
LC-MS/MS Assays

Education

Ph.D. in Analytical Chemistry
Master’s Degree
Bachelor’s Degree

Tools

Sciex Analyst Software
Watson LIMS

Job description

Job Title: Senior Scientist

Department:

Bioanalytical Services

Position Type: Full-time

Location: Exton, PA

Company Overview:

Frontage Laboratories Inc. is an award-winning, full-service CRO/Contract Research Organization with over 25 state-of-the-art laboratories across the US, Canada, and China. Our core competencies include drug metabolism, pharmacokinetics/pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Roles and Responsibilities:
  1. Validate unique scientific methods, assays, techniques, reports, etc. and run sensitive, reliable, and efficient LC-MS/MS bioanalytical assays for TK/PK assessment.
  2. Perform high-volume sample analysis, data analysis, quality control, and data interpretation.
  3. Maintain project schedules and timelines.
  4. Communicate project status, timelines, and data effectively with Principal Investigators, addressing any issues that arise.
  5. Handle method development and routine sample analysis projects concurrently, coordinating study activities to ensure efficiency and quality.
  6. Manage multiple projects simultaneously.
  7. Coordinate with Project Management and QC teams for timely sample analysis and results assessment.
  8. Assist in preparing study summaries and reports.
  9. Ensure regulatory compliance for each study and address QA audit findings.
  10. Maintain tools, computer programs, and SOPs needed for studies; research literature for new techniques and procedures to enhance capabilities.
  11. Assist in training and mentoring junior scientific staff, ensuring adherence to GLP regulations and SOPs.
  12. Set up, utilize, and maintain complex instrumentation while following safety precautions.
Qualifications and Skills:
  1. Understanding of experimental design, planning, data collection, and analysis software.
  2. Experience with Sciex Analyst software and Watson LIMS is a plus.
  3. Proven ability to work effectively in a team environment with excellent communication skills.
  4. Educational requirements:
    • Ph.D. in Analytical Chemistry, Biochemistry, Pharmacology, or related field with 1-2+ years of experience, OR
    • Master’s degree with 4+ years of experience, OR
    • Bachelor’s degree with 6+ years of experience.
Salary and Benefits:

We offer a competitive compensation and benefits package, including health and dental insurance, a 401(k) plan, life insurance, and more.

Equal Opportunity Employment:

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, disability, veteran status, or other protected characteristics.

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