Qureos Mentor

U.S. Pharmacopeia

<div><div><p><b>Description</b></p>
<p>At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.</p>
<p>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&mdash;regardless of background&mdash;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.</p>
<p><b>Brief Job Overview</b></p>
<p>This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.</p>
<p><b>How will YOU create impact here at USP?</b></p>
<p>As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.</p>
<p>Additionally, USP&rsquo;s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.</p>
<p>The Scientist-II has the following responsibilities:</p>
<ul><li><div>Executes all testing and analysis of data with excellence and essentially no errors.</div></li>
<li><div>
Supporting Verification, GPH, PQM, stability and other departmental teams in terms of testing whenever needed.</div></li>
<li><div>
Responsible for sample archival, sample tracking and chemical inventory tracking in the laboratory.</div></li>
<li><div>
Coordination with supervisor to ensure completion of the projects allotted to the team.</div></li>
<li><div>
Completing the project as per the timelines and troubleshoot the scientific aspects of the projects on need basis.</div></li>
<li><div>
Responsible for performing the calibration of the equipment as per the schedule.</div></li>
<li><div>
Responsible for preparing, executing, and completing IQ/OQ/PQ of new instruments.</div></li>
<li><div>
Ensuring that the chemicals and column etc. are available for the projects and forward the purchase requisitions.</div></li>
<li><div>
Taking up any additional responsibilities assigned by Supervisor from time to time.</div></li>
<li><div>
Ensure all lab safety and GLP practices are maintained in the lab and participate actively in the internal and external audits and certification.</div></li>
</ul>
<p><b>Who is USP Looking For?</b></p>
<p>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:</p>
<p>The candidate must have strong analytical chemistry knowledge with the ability to analyze, interpret and report effectively on data from a variety of analytical instrumental tests (e.g., HPLC, GC, Wet analytical techniques, spectroscopic techniques). Well-developed organizational and interpersonal skills. Able to establish and nurture relationships with individuals of varying backgrounds, cultures and learning styles.</p>
<ul><li>Master&rsquo;s degree in chemistry or Pharmacy.</li>
</ul>
<p>Experience:</p>
<ul><li><div>3 to 6 years with relevant laboratory experience.</div></li>
<li><div>
Proven track record of consistently delivering projects on time and with high quality for API&rsquo;s.</div></li>
<li><div>
Expert in chromatographic analysis, particularly in HPLC.</div></li>
<li><div>
Proficient in other related analytical instrumentation such as Water determination, Loss on drying, Residue on Ignition, Titrations, Spectroscopic analysis (UV, IR etc.,).</div></li>
<li><div>
Knowledge of pharmaceutical testing requirements and test protocols involving compendial methods for reference materials (USP compendia, ICH guidelines, FDA regulations etc.).</div></li>
<li><div>
Must possess effective communication skills, both written and verbal.</div></li>
<li><div>
Expert in Empower software with knowledge on Audit trails and Custom fields.</div></li>
<li><div>
Must possess good technical and analytical skills to independently resolve or troubleshoot issues.</div></li>
<li><div>
Should have a strong understanding of GLP regulations and exposure to external regulatory audits.</div></li>
</ul>
<p><b>Additional Desired Preferences</b></p>
<ul><li><div>Knowledge in other related analytical instruments (GC, Thermal, Elemental analysis, Mass analyzers etc.), Electronic Laboratory Notebook, ERP, QR coding system will be an added advantage.</div></li>
<li><div>
Understanding monograph procedures and participating in compendial methods for reference materials (USP, FCC, NF, etc.).</div></li>
<li><div>
Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&amp;D, or a contract pharmaceutical analytical laboratory testing organization is a plus.</div></li>
<li><div>
Awareness of GLP regulations, QMS, ISO/IEC 17025 and exposure to external regulatory audits is desirable.</div></li>
<li><div>
Ability to embrace and lead change. Extremely adaptable.</div></li>
</ul>
<p><b>Supervisory Responsibilities</b></p>
<p>None, this is an individual contributor role.</p>
<p><b>Benefits</b></p>
<p>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.</p>
<p>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.</p></div></div><p></p>
<br><p></p><div><p>Who is USP?</p><p>
The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide.
</p><p>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.
</p><p>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 work&mdash;an 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.</p></div>

Scientist II, RSL

<div><div><p><b>Description</b></p>
<p>At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.</p>
<p>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&mdash;regardless of background&mdash;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.</p>
<p><b>Brief Job Overview</b></p>
<p>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/General Chapters and maintaining safety and GLP environment in the lab. This position is a component of USP&rsquo;s core business, and the incumbent is expected to support monograph modernization initiatives.</p>
<p><b>How will YOU create impact here at USP?</b></p>
<p>As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.</p>
<p>Additionally, USP&rsquo;s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.</p>
<p>The Scientist IV has the following responsibilities:</p>
<ul><li><div>Engage in project planning, execution, method development and validation of projects according to set standards as USP general chapters, guidelines, SOPs and protocols.</div></li>
<li><div>
Apply technical and scientific expertise in analytical method development and validation of pharmaceuticals.</div></li>
<li><div>
Prepare and review the project plans, reports, laboratory notebook/ Laboratory management system (LMS) and compile project data as per requirement.</div></li>
<li><div>
Adhere to GLP and safety practices while working in the Lab.</div></li>
<li><div>
Practice Diversity, Equity, Inclusion, and Belonging principles at USP India.</div></li>
</ul>
<p><b>Who is USP Looking For?</b></p>
<p>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:</p>
<ul><li><div>Master&rsquo;s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 8-10 years of experience.</div></li>
<li><div>Strong knowledge in designing, executing, and interpreting extractables and leachables studies for packaging systems, medical devices, and drug products.</div></li>
<li><div>
Familiarity with regulatory requirements for E&amp;L in pharmaceutical and medical device sectors.</div></li>
<li><div>
Must have hands on experience in working with chemical methods and handling instruments like LC-MS, GC-MS.</div></li>
<li><div>
Strong expertise in mass spectrometry, including hands-on experience with HRMS, is required.</div></li>
<li><div>
Proficient in interpreting data using advanced mass spectrometry software tools.</div></li>
<li><div>
Understanding of USP/NF monographs/general chapters/general notices.</div></li>
<li><div>
Exposure to GMP/GLP/QMS environment and documentation procedures and champions the data integrity.</div></li>
<li><div>
Should be capable of performing analytical method developments and method validations using modern techniques and protocols.</div></li>
<li><div>
Good analytical skills in handling method development and Validations for Drug substances and Drug products.</div></li>
<li><div>
Should have exposure to GMP/GLP environment and documentation procedures.</div></li>
<li><div>
Awareness of ISO/IEC 17025 is desirable.</div></li>
</ul>
<p><b>Additional Desired Preferences</b></p>
<p>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.</p>
<ul><li><div>Exceptional breadth of pharmaceutical industry experience.</div></li>
<li><div>
Excellent technical writing and oral communication skills required.</div></li>
<li><div>
Must be able to communicate effectively with diplomacy and enthusiasm.</div></li>
<li><div>
Hands on experience in working with chemical methods and handling instruments like HPLC, GC, FTIR, UV-Visible.</div></li>
<li><div>
Technical and analytical skills required including the ability to interpret technical information.</div></li>
<li><div>
Should have good understanding of GLP regulations and exposed to external regulatory audits.</div></li>
</ul>
<p><b>Supervisory Responsibilities</b></p>
<p>None, this is an individual contributor role.</p>
<p><b>Benefits</b></p>
<p>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.</p>
<p>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.</p></div></div><p></p>
<br><p></p><div><p>Who is USP?</p><p>
The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide.
</p><p>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.
</p><p>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 work&mdash;an 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.</p></div>

Scientist IV, Compendial Development Laboratory (Extractables and Leachables)

<div><div><p><b>Description</b></p>
<p>At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.</p>
<p>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&mdash;regardless of background&mdash;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.</p>
<p><b>Brief Job Overview</b></p>
<p>This is a non-supervisory position to support development of Reference materials. The successful applicant in this role will work on projects including Analytical Method Development for in process samples for synthetic lab. The successful candidate will also perform a variety of non-routine and routine analytical tests, maintains safety &amp; GLP environment in the lab including evaluation of reference standards, development/validation (as per requirement) of official methods, stability studies and research projects in analytical department</p>
<p><b>How will YOU create impact here at USP?</b></p>
<p>As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.</p>
<p>Additionally, USP&rsquo;s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.</p>
<p>The Scientist III has the following responsibilities:</p>
<ul><li><div>[55%] Support to reaction monitoring, scale up and final analysis of samples as per monograph / in-house procedures including method development if required. Prepare development reports for Synthetic Support projects. Involve in project acceptance. Execute projects per the approved test protocols if assigned.</div></li>
<li><div>
[15%] Prepare, execute, and complete IQ/OQ/PQ of new instruments. Indent the required glass ware, chemicals, and columns for the ARD projects. Maintain GLP &amp; implement safety procedures while working in Lab. Perform other Projects whenever free from ARD activities. Perform other duties as assigned.</div></li>
<li><div>
[10%] Responsible for preparation of SOPs, protocols, reports, etc. Ensure the projects requirements by coordinating with the Purchasing department. Responsible for preparation of the records and documents. Ensure that the calibrations of the equipment&rsquo;s are performed as per the schedule</div></li>
<li><div>
[10%] Preparation and planning for ISO-9001 certification/recertification by participating actively, verification of protocols and related documents and take an active role in the internal as well as external QA audits and address the audit issues in a timely manner. Taking up any other additional responsibilities assigned by supervisor on a proactive basis and allotting additional responsibilities to the reporting staff in consultation with the supervisor. Participates in USP cross-functional teams as appropriate.</div></li>
<li><div>
[10%] Practice Diversity, Equity, Inclusion, and Belonging principles at USP India.</div></li>
</ul>
<p><b>Who is USP Looking For?</b></p>
<p>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:</p>
<ul><li><div>MSc. in Analytical Chemistry / Organic Chemistry/M. Pharm, having 6-8 years' experience in Analytical Research and Development or Ph.D. with 1-3 years of experience in Analytical Research and Development</div></li>
<li><div>
Must have hands on experience in working with chemical methods and handling instruments like HPLC, GC, FTIR, UV-Visible, wet chemistry, etc.</div></li>
<li><div>
Experience in analytical testing and development with focus on process analytical chemistry. Exposure to GMP/GLP environment and documentation procedures required.</div></li>
<li><div>
A comprehensive understanding of the science involved in the development of synthetic organic molecules and analytical chemistry.</div></li>
<li><div>
Ability to perform analytical method developments and method validations as and when required.</div></li>
<li><div>
Excellent technical writing and verbal communication skills are required.</div></li>
<li><div>
Good interpersonal skills and proven ability to function in a team-oriented environment are necessary.</div></li>
</ul>
<p><b>Additional Desired Preferences</b></p>
<ul><li><div>Knowledge of handling LCMS, GCMS, IC and ICP-MS will be an added advantage.</div></li>
<li><div>
General chapter information, ELN, Empower and NuGenesis will be added advantage.</div></li>
<li><div>
Able to communicate effectively with both internal and external customers. Preferably familiar with electronic notebook documentation of experimental procedures.</div></li>
<li><div>
Skilled in evaluation and interpretation of data; Ability to multi-task.</div></li>
<li><div>
Skilled in anticipating, troubleshooting, and solving technical problems.</div></li>
<li><div>
Takes personal responsibility to ensure work is delivered on time and is of the highest quality.</div></li>
</ul>
<p><b>Supervisory Responsibilities</b></p>
<p>NA</p>
<p><b>Benefits</b></p>
<p>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.</p>
<p>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</p></div></div><p></p>
<br><p></p><div><p>Who is USP?</p><p>
The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide.
</p><p>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.
</p><p>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 work&mdash;an 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.</p></div>

Scientist III, ARD

Join U.S. Pharmacopeia and explore 3   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

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Scientist II, RSL

Scientist IV, Compendial Development Laboratory (Extractables and Leachables)

Scientist III, ARD