USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
Post : Technical Associate, CDL
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.
Job Description
The Technical Associate has the following responsibilities :
• Engage in project planning, execution, method development and validation of projects according to set standards as USP general chapters, guidelines, SOPs and protocols. Apply technical and scientific expertise in analytical method development and validation of Small molecule projects.
• Prepare the 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.
Candidate Profile
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 0-1 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 the 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 substance and drug products.
• Awareness of ISO ISO/IEC 17025 is desirable.
• Should have fair understanding of GLP regulations and exposed to external regulatory audits.
• Should possess technical knowledge in the areas of Drug substance, Drug products and different dosage forms.
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 disqualifies for candidate consideration.
• 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.
Additional Information
Experience : 0-1 years
Qualification : MSc
Location : Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : CDL
End Date : 10th January 2025
CDL Technical Associate : Apply here
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