Freshers Chemistry Job Opening – Apply Online at USP
Looking for a Technical Associate or Scientist I role at USP? This is an exciting opportunity to work in the Compendial Development Laboratory (CDL) in Hyderabad, contributing to analytical method development and validation for pharmaceuticals. If you have a Master’s in Chemistry or Pharmaceutical Sciences, apply now!
About the Company
United States Pharmacopeia (USP) is a global, independent, scientific nonprofit organization that sets public quality standards for medicines, dietary supplements, and food ingredients. With a mission to improve global health, USP works with regulatory agencies, pharmaceutical companies, and healthcare organizations to ensure the quality, safety, and efficacy of medical products worldwide. USP’s Compendial Development Laboratory (CDL) in Hyderabad plays a crucial role in pharmaceutical testing, method development, and validation, supporting global drug quality initiatives.
Job Description
Job Posting: Technical Associate / Scientist I, CDL
Location: Hyderabad, IND
Job Category: Chemistry & Scientific Standards
Job Type: Full-Time
Req ID: SCIEN002662
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 a 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 an 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.
Responsibilities of Technical Associate/S-I
- 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 pharmaceuticals.
- Prepare and review project plans, reports, laboratory notebooks/Laboratory Management System (LMS), and compile project data as required.
- 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:
Experience for Technical Associate
Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 0-1 years of experience in the relevant field.
Experience for S-I
Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 1-3 years of experience in the relevant field.
Skill set required for USP Technical Associate Job
- Possess a fine understanding of USP/NF monographs, general chapters, and general notices.
- Exposure to GMP/GLP/QMS environment and documentation procedures, and champions data integrity.
- Capable of performing analytical method development and validations using HPLC and GC techniques and protocols.
- Analytical skills in handling method development and validations for drug substances, drug products.
- Should have exposure to GMP/GLP environment and documentation procedures.
- Awareness of ISO/IEC 17025 is desirable.
Additional Desired Preferences
- Exceptional breadth of pharmaceutical industry experience.
- Excellent technical writing and oral communication skills required.
- Must be able to communicate effectively with diplomacy and enthusiasm.
- Technical and analytical skills required, including the ability to interpret technical information.
- Must have hands-on experience in working with chemical methods and handling instruments like UHPLC, FTIR, KF and UV-Visible.
- Should have a good understanding of GLP regulations and exposure to external regulatory audits.
Supervisory Responsibilities: NA
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
Keywords: Technical Associate, Scientist I, CDL, Chemistry, Scientific Standards, USP, Analytical Method Development, GLP, Pharmaceutical Sciences, Freshers Chemistry Job Opening – Apply Online at USP
