U.S. Pharmacopeial Convention Jobs

Job Information

The U.S. Pharmacopeial Convention (USP) Scientist I, ARD in Hyderabad, India

Description

Roles and Responsibilities

  • Perform literature search, plan, and execute compendial procedures as per protocols, guidelines, and established SOPs under the supervision of senior member.

  • Ensure the projects requirements are met by coordinating with other team members and thesupervisor

  • 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 ProceduresRoles and Responsibilities

  • Perform literature search, plan, and execute compendial procedures as per protocols, guidelines, and established SOPs under the supervision of senior member.

  • Ensure the projects requirements are met by coordinating with other team members and thesupervisor

  • 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

Basic Qualifications

  • Sc. 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.

Job Category Chemistry & Scientific Standards

Job Type Full-Time

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