U.S. Pharmacopeial Convention (USP) Hiring ARD Chemistry Scientist
The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed, and consumed worldwide. Check out all the details
Job Title: Scientist I, ARD
Location: Hyderabad, India
Basic Qualifications
- MSc. in Analytical Chemistry / Organic Chemistry, from a well-recognized University in India or abroad and required not less than 1-3 years’ experience in Analytical lab.
- Must have hands on experience in working with chemical methods and handling instruments like HPLC, GC, FTIR, UV-Visible, wet chemistry, etc.
- Good technical writing and verbal communication skills are required. Good interpersonal skills and proven ability to function in a team-oriented environment are necessary. Understanding of GMP / ISO-IEC 17025 Guidelines is a requirement
Preferred Qualifications
- Proficient with pharmaceutical testing requirements involving compendial methods for reference materials.
- Expert in HPLC and GC analysis and troubleshooting, proficient in other related analytical instrumentation (IR, KF, UV, and thermal analysis techniques etc.).
- Working knowledge of computer applications, such as MS Word and MS Excel are required.
- Good interpersonal skills and proven ability to function in a team-oriented environment are necessary.
- Proven track record of consistently delivering projects on time and with high quality.
- Prior experience in a high-volume pharmaceutical ARD laboratory or contract pharmaceutical analytical laboratory testing organization is a plus.Takes personal responsibility for delivery of projects to customers.
Roles and Responsibilities U.S. Pharmacopeial Convention (USP)
- Perform literature search, plan, and execute compendial procedures as per protocols, guidelines, and established SOPs under the supervision of senior members.
- Ensure the requirements of the project are met by coordinating with other team members and the supervisor
- Ensure the project updates are provided to the supervisor on weekly basis.
- Engage in project planning, execution, method development, and analysis of test samples according to set standards as USP general chapters, guidelines, SOPs, and protocols.
- Monitor each stage of development closely and coordinate with the supervisor to complete the projects within time.
- Responsible for archival of projects
- Ensure that the calibrations of the equipment are performed as per the schedule and assist in preparation, execution, and completion of IQ/OQ/PQ for new instruments.
- Support lab ERP coordinator to maintain the inventory of chemicals and LC columns.
- Work professionally and collaboratively with fellow lab scientists and other relevant departments in the development of reference standards.
- Identify and implement solutions to technical problems related to the development and analysis of the data.
- Implement and maintain key quality systems such as deviations, investigations, and CAPAs. Maintain GLP & safety procedures while working in Lab, in addition to ISO 9001 – ISO/IEC 17025 requirements.
- Ensure to follow USP Policies and ProceduresRoles and Responsibilities
- Perform literature search, plan, and execute compendial procedures as per protocols, guidelines, and established SOPs under the supervision of senior members.
- Ensure the requirements of the project are met by coordinating with other team members and the supervisor
- Ensure the project updates are provided to the supervisor on weekly basis.
- Engage in project planning, execution, method development and analysis of test samples according to set standards as USP general chapters, guidelines, SOPs, and protocols.
- Monitor each stage of development closely and coordinate with supervisor to complete the projects within time.’
- Responsible for archival of projects
- Ensure that the calibrations of the equipment’s are performed as per the schedule and assist in preparation, execution, and completion of IQ/OQ/PQ for new instruments.
- Support lab ERP coordinator to maintain the inventory of chemicals and LC columns.
- Work professionally and collaboratively with fellow lab scientists and other relevant departments in the development of reference standards.
- Identify and implement solutions to technical problems related to the development and analysis of the data.
- Implement and maintain key quality systems such as deviations, investigations, and CAPAs. Maintain GLP & safety procedures while working in Lab, in addition to ISO 9001 – ISO/IEC 17025 requirements.
- Ensure to follow USP Policies and Procedures
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