USP Pharma Scientist Job Opening! MPharma & PhD Apply
Scientist III, Reference Standards Evaluation
Hyderabad, IND
Job Category: Chemistry & Scientific Standards
Job Type: Full-Time
Req ID: SCIEN002565
Description
Brief Job Overview
This is a hands-on, non-supervisory position responsible for the oversight and successful implementation and completion of all activities pertaining to a portfolio of Reference Standards (RS)/Material Strategy program (CRM/ARM etc.). The incumbent is responsible for the timely preparation of procurement specifications and collaborative testing protocols for all RS lots, providing technical assistance to collaborating labs, reviewing analytical data, preparing summary reports, and drafting packaging and Quality Control testing instructions.
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. Additionally, USP is committed to the professional development of its employees by providing training in inclusive management styles and other competencies to foster engaged and productive work environments.
The SIII position has the following responsibilities:
- Responsible for timely preparation of collaborative testing protocols for new/replacement RS lots and providing technical assistance for collaborating labs.
- Reviewing analytical data received from collaborators, preparing summary reports, and drafting RSCEP packages, packaging instructions, and QC testing instructions while assigning periodic re-test intervals.
- Independently maintaining successful scheduling operations, necessary documentation, complete and accurate information, and addressing quality issues to ensure availability of reference standards in a complex portfolio.
- Drafting product planning documents (PPD), coordinating with labs, and reviewing/interpreting data from international collaborative studies.
- Coordinating any additional necessary testing and assisting other staff members in addressing comments.
- Providing correct guidance on interpreting test data and proposing and designing studies to obtain necessary data to resolve complaints.
- Supporting the Documentary Standard team through peer review of draft monographs.
- Supporting the Material Strategy program (CRM, ARM).
- Demonstrating technical understanding to internal and external audiences regarding USP’s Reference Standards program.
- Engaging in conversations about reference standards issues and addressing general customer technical inquiries. Investigating customer complaints thoroughly with minimal guidance.
- Presenting information to USP staff and external audiences.
- Facilitating additional cross-functional activities with other departmental and USP staff.
- Performing other related duties as assigned.
Who is USP Looking For?
The successful candidate will have a demonstrated understanding of our mission, a commitment to excellence through inclusive and equitable behaviors and practices, the ability to quickly build credibility with stakeholders, and the following competencies and experience:
- MSc/MPharm with 6–8 years of experience.
- Ph.D. with 1–3 years of experience.
Additional Desired Preferences:
- Ability to read and interpret spectroscopic analyses data (NMR, IR, MS, Raman, XRD, etc.).
- Hands-on experience with chromatographic techniques (HPLC, GC, SFC).
- Ability to handle multiple priorities in a fast-paced environment.
- Excellent written and verbal communication skills.
Keywords: Spectroscopic analyses, Chromatographic techniques, Quality Control testing. USP Pharma Scientist Job Opening! MPharma & PhD Apply. Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.
