The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide.
Post : Scientist I, Verification Program
Job Description
Brief Job Overview
This is non-supervisory role involves conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) utilizing suitable methods. The Scientist will enhance the laboratory's scientific proficiency and work ethic by offering extensive technical support and knowledge. Proficient in numerous common laboratory techniques, the Scientist is capable of providing valuable observations and insights into challenging projects. The individual in this role will furnish technical aid to the Verification Program by executing analytical tests and preparing comprehensive summary reports.
Job Description
• Conducts Verification projects (Dietary supplements/Dietary Ingredients) by performing individual analytical tests assigned by the Team Leader.
• Completes projects within designated timelines and priorities.
• Demonstrates a robust scientific approach to laboratory analysis.
• Regularly utilizes personal experience, academic training, and technical insights, including emerging sciences, to address complex technical issues within the laboratory.
• Compiles project reports and responds to QA observations.
• Executes all testing and data analysis with precision, minimizing errors.
• Shows a strong commitment to continuous learning and personal development.
• Proposes and implements new approaches or processes to enhance laboratory operations.
• Influences project direction positively by aligning own work with the overall direction of laboratory projects.
• Assists with additional testing programs and laboratory maintenance tasks as required.
• Ensures compliance with Good Laboratory Practices (GLP) and safety systems in the laboratory.
• Maintains equipment calibration according to the schedule.
• Coordinates the procurement of chemicals, columns, glassware, etc., in advance, in coordination with lab operations and the purchase department, considering project deadlines.
• Adheres to US Pharmacopeia (USP) mission, policies, and procedures.
• Cultivates positive relationships with Quality Assurance (QA), Human Resources (HR), Purchase, Accounting, IT, and other departments.
• Participates actively in the preparation and planning for ISO-9001 & ISO-17025 certification/recertification, including taking an active role in internal QA and external audits and addressing audit issues promptly.
• Supports Global Public Health (GPH), Reference Standard Laboratory (RSL), and other departmental teams as required for analytical testing, review, execution, and approval
Candidate Profile
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
• Master’s degree in pharmacy or Analytical chemistry.
• Minimum 1 to 3 years with relevant laboratory experience.
• Previous engagement in a high-volume pharmaceutical manufacturing QC laboratory or a contract pharmaceutical analytical testing laboratory, specifically pertaining to pharmaceutical dosage forms such as oral and liquid
• Strong preference for candidates with expertise in HPLC operation using Empower software, as well as proficiency in dissolution analysis.
Additional Information
Experience : 1 to 3 years
Qualification : MSc or M.Pharm
Location : Hyderabad, IND
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Verification Program
End Date : 30th December 2024
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