Postdoctoral Scientist

Jobtailor

Town of Newark (WI)

On-site

USD 100,000 - 150,000

Full time

6 days ago
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Job summary

Jobtailor is seeking a PhD-level scientist to lead method development and validation studies using LC-(HR)MS/MS for TK/PK/biomarker assessment in a GLP-compliant environment.

The role requires hands-on MS expertise, protocol development, data interpretation, and dedication to regulatory compliance. Responsibilities include instrument maintenance, QA documentation, and managing project timelines in a bioanalytical services setting.

Qualifications

  • Ph.D. in Analytical Chemistry, Biochemistry, Microbiology, Pharmacology, Food Science, Plant Science or related scientific discipline.
  • Hands-on experience in mass spectrometry.
  • Ability to independently manage one or more method development/validation studies with minimum supervision.
  • Ability to prepare, review, and understand study protocols
  • Ability to evaluate data significance and report findings
  • Ability to prepare study summaries and reports
  • Ability to set up, utilize, and maintain complex instrumentation
  • Ability to maintain regulatory compliance and prepare QA-related documents
  • Ability to address QA audit findings
  • Ability to maintain project schedules and timelines
  • Experience developing, validating, and running LC-(HR)MS/MS assays for TK/PK/biomarker assessment
  • Knowledge of GLP regulations and SOPs
  • Ability to follow GLP regulations and SOPs in bioanalytical service activities

Responsibilities

  • Independently manage one or more method development and validation studies
  • Prepare, review, and understand study protocols
  • Evaluate data significance and report findings
  • Prepare study summaries and reports
  • Set up, utilize, and maintain complex instrumentation
  • Maintain regulatory compliance for each study
  • Prepare QA-related documents and address QA audit findings
  • Maintain project schedules and timelines
  • Develop, validate, and run LC-(HR)MS/MS assays for TK/PK/biomarker assessment
  • Ensure GLP regulations and SOPs are followed in bioanalytical service activities
  • Support QPS’s bioanalytical capabilities for biomarker quantitation

Skills

Mass Spectrometry
LC-(HR)MS/MS
Method Development
Method Validation
Study Protocol Preparation
Data Evaluation
Instrumentation Maintenance
Project Management
Biomarker Quantitation
GLP Regulations
SOP Compliance

Education

Ph.D. in Analytical Chemistry or related scientific discipline

Job description

  • Independently manage one or more method development and validation studies
  • Prepare, review, and understand study protocols
  • Evaluate data significance and report findings
  • Prepare study summaries and reports
  • Set up, utilize, and maintain complex instrumentation
  • Maintain regulatory compliance for each study
  • Prepare QA-related documents and address QA audit findings
  • Maintain project schedules and timelines
  • Develop, validate, and run sensitive, reliable, and efficient LC-(HR)MS/MS assays for TK/PK/biomarker assessment
  • Ensure GLP regulations and SOPs are followed in bioanalytical service activities
  • Support QPS’s bioanalytical capabilities for biomarker quantitation
Requirements
  • Ph.D. in Analytical Chemistry, Biochemistry, Microbiology, Pharmacology, Food Science, Plant Science or related scientific discipline
  • Hands-on experience in mass spectrometry
  • Ability to independently manage one or more method development/validation studies with minimum supervision
  • Ability to prepare, review, and understand study protocols
  • Ability to evaluate data significance and report findings
  • Ability to prepare study summaries and reports
  • Ability to set up, utilize, and maintain complex instrumentation
  • Ability to maintain regulatory compliance and prepare QA-related documents
  • Ability to address QA audit findings
  • Ability to maintain project schedules and timelines
  • Experience developing, validating, and running LC-(HR)MS/MS assays for TK/PK/biomarker assessment
  • Knowledge of GLP regulations and SOPs
  • Ability to follow GLP regulations and SOPs in bioanalytical service activities
Core Competencies

Demonstrates expertise in method development and validation, particularly in LC-(HR)MS/MS assays for TK/PK/biomarker assessment, while ensuring compliance with GLP regulations and SOPs. Proficient in managing complex instrumentation and preparing comprehensive study documentation.

Highest-signal resume keywords
  • Ph.D. In Analytical Chemistry
  • Mass Spectrometry Experience
  • LC-(HR)MS/MS Assay Development
  • Regulatory Compliance Knowledge
  • QA Document Preparation
ATS Optimization Keywords
Hard Skills
  • Method Development
  • Method Validation
  • Data Evaluation
  • Study Protocol Preparation
  • Assay Development
  • Instrumentation Maintenance
  • Project Management
  • Biomarker Quantitation
  • GLP Regulations
  • SOP Compliance
Soft Skills
  • Independent Management
  • Attention To Detail
  • Effective Communication
  • Problem Solving
  • Time Management
Industry Keywords
  • Bioanalytical Services
  • TK/PK Assessment
  • Quality Assurance
  • Regulatory Compliance
  • Audit Findings
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