Scientist I CDL
Scientist I CDL
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Job Description
Who is USP
The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the worlds top authorities in health and science to develop quality standards for medicines dietary supplements and food ingredients. USPs fundamental belief that Equity Excellence manifests in our core value of Passion for Quality through our more than 1300 hardworking professionals across twenty global locations to deliver the mission to strengthen the supply of safe quality medicines and supplements worldwide.
At USP we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create the partnerships we build and the conversations we foster we affirm the value of Diversity Equity Inclusion and Belonging in building a world where everyone can be confident of quality in health and healthcare.
USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our workan environment where every employee feels fully empowered and valued irrespective of but not limited to race ethnicity physical and mental abilities education religion gender identity and expression life experience sexual orientation country of origin regional differences work experience and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.
Brief Job Overview
This is a nonsupervisory 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 USPs 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 USPs public health mission of increasing equitable access to highquality 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 Technical associate/SI has the following responsibilities:
- Engage in project planning 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:
- Masters Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 01 years of experience in the relevant field.
Experience for SI:
- Masters Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 13 years of experience in the relevant field.
Skill set required:
- 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 handson experience in working with chemical methods and handling instruments like UHPLC FTIR KF and UVVisible.
- 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 companypaid time off and comprehensive healthcare options to retirement savings you can have peace of mind that your personal and financial wellbeing 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 specificwritten agreement with USP
Employment Type
Full-Time
