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Principal Research Scientist at BioPharma Services
Job Description & How to Apply Below
In this full-time onsite role, you will oversee method development while ensuring compliance with GLP standards. Your responsibilities include coordinating complex projects, providing technical guidance, and engaging with regulatory agencies on Deficiency Letters. You'll also be responsible for project feasibility studies and generating analytical reports for submission to regulatory bodies.
Key Responsibilities:
• Conduct bioanalytical method development using LC-MS/MS
• Provide technical oversight to research scientists
• Coordinate and organize large complex projects
• Assist in responding to Deficiency Letters from regulatory bodies
• Document and report study deviations promptly
Requirements:
• MSc or Ph.D. in Analytical Chemistry or related field
• Minimum 5 years relevant experience with LC-MS/MS
• Strong knowledge of GLP and regulatory compliance
• Excellent communication and organizational skills
• Ability to work safely and comply with health precautions
Bring your expertise in LC-MS/MS to lead innovative research solutions at Bio Pharma Services Inc.
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