Technical Associate, Toxicology
Location: Hyderabad, India
Job Category: Chemistry & Scientific Standards
Job Type: Full-time
Req ID: TECHN002660
Job Overview:
The Technical Associate in Toxicology supports the standard-setting activities of the USP-NF. This hands-on, non-supervisory role is responsible for evaluating literature related to the safety of dietary supplements and herbal medicines. The incumbent helps determine the suitability of these products for inclusion in the USP-NF monograph development process by conducting literature searches, analyzing data, and writing reports.
Key Responsibilities:
Literature Search & Analysis:
Perform literature searches on the safety and toxicology of botanicals and dietary ingredients.
Analyze and synthesize literature data, focusing on safety and toxicological assessments.
Quality Assessment & Coordination:
Conduct quality assessments of studies used in the admission evaluation of dietary supplements and herbal medicines.
Coordinate with cross-functional teams to ensure efficient workflows throughout the standard-setting process.
Publication & Reporting:
Contribute to the publication of admission evaluation summaries for the Dietary Supplement Compendium (DSC).
Write clear and concise reports on the safety of botanicals and other dietary ingredients.
Other Duties:
Perform any other related duties as required by the team or organization.
Qualifications:
Education & Experience:
M. Pharm (Pharmacology and/or Toxicology), MSc (Toxicology/Clinical Research), or a related discipline with 0-1 year of relevant experience in botanicals, dietary ingredients, or chemical safety assessment.
Skills & Expertise:
Basic understanding of toxicological principles and guidelines.
Ability to perform literature searches, analyze data, and interpret findings.
Strong written and verbal communication skills, essential for sharing information with both scientific and non-technical staff.
Ability to establish and nurture relationships with colleagues from diverse backgrounds.
Additional Desired Preferences:
Basic knowledge of clinical studies, OECD toxicological guidelines, pharmacokinetics, and regulatory opinions/information (e.g., EMA, EFSA, GRAS).
Familiarity with databases used to extract toxicological information on chemicals and botanicals.
Basic knowledge of pharmacognosy or natural product chemistry.
Understanding of global regulatory guidance on dietary supplements nomenclature and labeling.
Fundamental knowledge of hazard and risk assessment of chemicals.
Ability to prioritize tasks and manage multiple projects simultaneously.
Adaptability to changing work plans based on organizational needs.
Effective interpersonal communication, writing, listening, and presentation skills.
Benefits:
USP offers a comprehensive benefits package to support the well-being of employees, including healthcare options, retirement savings, and company-paid time off.
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