MSc Chemistry Laboratory Scientist Vacancy @ USP – Apply Online
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Job Title: Scientist I – Compendial Development Laboratory
Location: Hyderabad, India
Basic Qualifications
- Master’s Degree in Chemistry with 1-3 years of experience. Possess a fine understanding of USP/NF/FCC monographs/general chapters/general notices. Exposure to GMP/GLP/QMS environment and documentation procedures and champions data integrity.
- Should be capable of performing analytical method developments and method validations using modern techniques and protocols. Good analytical skills in handling method development and Validations for Drug substances, Drug products, Food ingredients and food products.
- Should have exposure to GMP/GLP environment and documentation procedures. Awareness of ISO/IEC 17025 is desirable.
Preferred Qualifications
- Master’s Degree in Chemistry (Analytical / Organic) or Pharmaceutical Sciences with 1-3 years of experience. Excellent technical writing and oral communication skills are required.
- Must be able to communicate effectively with diplomacy and enthusiasm. Technical and analytical skills are required including the ability to interpret technical information.
- Must have hands-on experience in working with chemical methods and handling instruments like HPLC, UHPLC, LC-MS, GC, GC-MS, FTIR, and UV-Visible. Should have a fair understanding of GLP regulations and be exposed to external regulatory audits.
Summary of the Position:
This is a non-supervisory position in the Compendial Development Laboratory (CDL) within Global Laboratory Operations. The incumbent will be responsible for performing analytical method development and validations for USP/NF monographs and maintaining safety and GLP environment in the lab. This position is a component of USP’s core business, and the incumbent is expected to support monograph modernization initiatives.
Roles and Responsibilities
- Search relevant literature for the USP/NF monograph modernization projects.
- Responsible for the complete lifecycle of the monograph modernization/development project (initiation, execution, reporting, & completion).
- Responsible for method development and validations (DS/DP/Excipients), using chromatography (HPLC, GC) techniques.
- Should have worked on chromatography (HPLC, GC) techniques.
- Should have experience of method development and validations (DS/DP/Excipients).
- Responsible for design, review, and execution of method development experiments and performing method validation in accordance with laid down procedure.
- Responsible for the preparation of method validation protocols and reports.
- Engage in project planning, execution, method development, and validation according to set standards as USP general chapters, guidelines, SOPs, and protocols.
- Plan individually the project requirements and their completion within the timelines by coordinating with the supervisor and team.
- Responsible for regular maintenance of assigned instruments.
- Ensure that the calibrations of the equipment are performed as per the schedule.
- Responsible for review of IQ/OQ/PQ documents of instruments.
- Indent the required glassware, chemicals, and columns for the CDL projects.
- Maintain GLP & safety procedures while working in Lab.
Benefits
USP provides you with the benefits you need to protect yourself and your family today and tomorrow. From company-paid time off, and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial wellbeing are protected.
Apply Online
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