Pharmaceutical Sciences Job at USP – Apply For Scientist Role
Scientist I, CDL
Hyderabad, IND
Job Category: Chemistry & Scientific Standards
Job Type: Full-Time
Req ID: SCIEN002525
Description
Brief Job Overview
This is a non-supervisory position in the Compendial Development Laboratory (CDL) within Global Laboratory Operations. The incumbent will be responsible for performing analytical method development and validations for USP/NF monographs and maintaining safety and GLP environment in the lab. This position is a component of USP’s core business, and the incumbent is expected to support monograph modernization initiatives.
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 Scientist-I has the following responsibilities:
- Engage in project planning, execution, method development, and validation of projects according to set standards such as USP general chapters, guidelines, SOPs, and protocols.
- Apply technical and scientific expertise in analytical method development and validation of small molecule projects.
- Prepare project plans, reports, laboratory notebook/Laboratory management system (LMS), and compile project data as per requirement.
- Adhere to GLP and safety practices while working in the lab.
- Practice Diversity, Equity, Inclusion, and Belonging principles at USP India.
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 chemistry with 1-3 years of experience.
- Possess a fine understanding of USP/NF monographs/general chapters/general notices.
- Exposure to GMP/GLP/QMS environment and documentation procedures and champions data integrity.
- Should be capable of performing analytical method developments and method validations using modern techniques and protocols.
- Good analytical skills in handling method developments and validations for drug substances and drug products.
- Awareness of ISO/IEC 17025 is desirable.
Additional Desired Preferences
Desired preferences are to showcase any additional preferred levels of expertise to perform the role. Reminder: any items listed in this section are not requirements nor disqualifiers for candidate consideration.
- Master’s degree in chemistry or Pharmaceutical Sciences with 1-3 years of experience in a relevant field.
- Must have hands-on experience in working with chemical methods and handling instruments like HPLC, GC, IC, ICP-OES/MS, FT-IR, UV-Visible, AAS, and KF.
- Should have a fair understanding of GLP regulations and be exposed to external regulatory audits.
- Should possess technical knowledge in the areas of drug substances, drug products, and different dosage forms.
- Technical and analytical skills required including the ability to interpret technical information.
- Exceptional breadth of Pharma industry experience.
- Excellent technical writing and oral communication skills required.
- Must be able to communicate effectively with diplomacy and enthusiasm.
Supervisory Responsibilities: NA
Link to Original Notification to apply: Apply here
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