USP Scientist Job MPharma & Analytical Chemistry – Apply Online
Scientist I, Verification Program
Hyderabad, IND
Job Category: Chemistry & Scientific Standards
Job Type: Full-Time
Req ID: SCIEN002568
Description
Brief Job Overview
This is a non-supervisory role that 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.
How will YOU create impact here at USP?
In this role at USP, you contribute to USP’s public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments.
Key Responsibilities:
- 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.
Who is USP Looking For?
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 Desired Preferences:
- Proficiency in leading projects to completion with a high level of scientific expertise, including extensive knowledge of pharmaceutical testing requirements and test protocols encompassing compendial methods (USP, BP, EP, etc.).
- Preference for expertise in GC operation with Empower software, as well as proficiency in ICP-OES, ICP-MS and LC-MS with troubleshooting abilities.
- Additionally, adept in operating and troubleshooting other related analytical instrumentation (IR, KF, UV, Ion chromatography, wet analysis, etc).
- Exceptional communication and presentation skills, both verbal and written, with a preference for candidates experienced in the pharmaceutical industry.
- Familiarity with ICH guidelines and FDA regulations, along with experience in compendial procedures and compliance, is highly desired.
- Proficiency in Electronic Laboratory Notebook (ELN) is also preferred.
- Demonstrates a personal commitment to ensuring timely delivery of high-quality work and possesses the skills to anticipate, troubleshoot, and resolve technical challenges.
Supervisory Responsibilities: No
To apply for this position, visit the original notification here.
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