Scientist Iv

**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.). This incumbent is responsible for the timely preparation of procurement specification and collaborative testing protocols for all RS lots, technical assistance for collaborating labs, analytical data review and preparation of summary reports, preparation of 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. 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.

The SIII/SIV position has the following responsibilities:
- Responsible for timely preparation of collaborative testing protocols for new/replacement RS lots, technical assistance for collaborating labs- To review the analytical data received from the Collaborators and to prepare summary reports and RSCEP packages, preparation of packaging and QC testing instructions and assigning periodic re-test intervals. Independently maintains successful scheduling operations, necessary documents, complete and accurate information; and addresses quality issues to ensure availability of reference standards in a complex portfolio.- To Draft product planning documents (PPD), coordinates with labs, and reviews/interprets data from international collaborative studies.- To Coordinates for any additional necessary testing and assists other staff members in addressing the comments.- To provide correct guidance on the interpretation of test data, Proposes and designs studies to obtain necessary data to resolve complaints.- To support Documentary Standard team by peer review of draft monograph- To demonstrate technical understanding to internal and external audiences regarding USP's Reference Standards program.- Engages in conversation about reference standards issues. Addresses general customer technical inquiries and thoroughly investigates customer complaints with mínimal guidance.- Presents information to USP staff and external audiences.- Facilitates additional cross-functional activities with other departmental staff and other USP staff.- Performs other related duties as assigned.

**Who is USP Looking For?**

**Scientist IV**

MSc/MPharm with 8-10 yrs of experience (or) Ph.D. with 3-5 yrs of experience

**Scientist III**:
MSc/MPharm with 6-8 yrs of experience (or) Ph.D. with 1-3 yrs of experience- Ability to read and interpret spectroscopic analyses data (NMR, IR, MS etc.)- Hands on experience on chromatographic techniques (HPLC, GC)- Ability to handle multiple priorities in a fast-paced environment.- Excellent written and verbal communications skills.

**Additional Desired preferences**- Hands on experience spectroscopic analyses data (NMR, IR, MS etc.) and knowledge on chromatographic techniques.- XRD, Polymorphic studies exposure- Stability studies exposure

**Supervisory Responsibilities: NA**

If yes, what is the number of direct reports and their titles?

**Benefits**

USP provides the benefits 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 well-being is protected.

Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.