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scientific associate director - pharmacokinetics and drug metabolism (small molecule adme lab lead) Jobs in Hyderabad

scientific associate director - pharmacokinetics and drug metabolism (small molecule adme lab lead)

senior research scientist

PI Health Sciences Ltd

<div>
 
 About the job
 
 
 
 
 
 
 Senior Research Scientist : Synthesis R&amp;D
 
 
 
 
 
 
 
 Purpose of the Role:
 
 
 
 To contribute to early-stage drug discovery programs by designing and synthesizing novel small molecules that meet client objectives. The role supports hit-to-lead and lead optimization efforts through data-driven medicinal chemistry strategies, with the goal of delivering high-quality drug candidates in a collaborative CRO environment.
 
 
 
 
 
 
 Key Responsibilities:
 
 
 
 
 Strategic &amp; Scientific:
 
 
 <ul>
 <li>
 Design and synthesize novel chemical entities (NCEs) guided by SAR and target profile.
 </li>
 <li>
 Contribute to lead identification and optimization in FTE or integrated drug discovery (IDD) projects.
 </li>
 <li>
 Collaborate with cross-functional teams (e.g., biology, ADME, computational chemistry) to advance candidate selection.
 </li>
 <li>
 Analyze biological and ADME data to refine compound design strategies.
 </li>
 </ul>
 
 
 Operational:
 
 
 <ul>
 <li>
 Plan and execute multistep organic syntheses with minimal supervision.
 </li>
 <li>
 Characterize compounds using NMR, LCMS, HPLC, and other analytical tools.
 </li>
 <li>
 Maintain detailed and accurate experimental records (ELN/lab notebooks).
 </li>
 <li>
 Deliver high-purity compounds on time to meet client/project goals.
 </li>
 </ul>
 
 
 Collaboration &amp; Communication:
 
 
 <ul>
 <li>
 Actively participate in team meetings, project reviews, and client discussions.
 </li>
 <li>
 Coordinate with analytical and biology teams for data turnaround and integration.
 </li>
 <li>
 Present experimental results and SAR insights to internal and external stakeholders.
 </li>
 </ul>
 
 
 Compliance &amp; Documentation:
 
 
 <ul>
 <li>
 Follow lab safety protocols and maintain GLP/GMP (where applicable).
 </li>
 <li>
 Ensure adherence to SOPs and maintain project documentation for IP protection and client reporting.
 </li>
 </ul>
 
 
 
 
 
 Qualification &amp; Experience:
 
 
 <ul>
 <li>
 M.Sc. with 3&ndash;8 years of relevant experience in a CRO environment.
 </li>
 <li>
 Proven expertise in synthetic organic chemistry and medicinal chemistry principles.
 </li>
 <li>
 Experience in client-facing discovery projects is strongly preferred.
 </li>
 </ul>
 
 
 
 
 
 Key Skills &amp; Competencies:
 
 
 <ul>
 <li>
 Deep understanding of SAR, pharmacophores, and drug-likeness criteria.
 </li>
 <li>
 Strong skills in synthetic planning, reaction optimization, and troubleshooting.
 </li>
 <li>
 Excellent communication and data presentation abilities.
 </li>
 <li>
 Ability to multitask and work effectively in a high-paced, collaborative environment.
 </li>
 </ul>
 
 
</div>

Research And Development Scientist

US Pharmacopeia

<div>
 
 Description
 
 
 
 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.
 
 
 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.
 
 
 
 Brief Job Overview
 
 
 
 This is a professional, highly technical, non-supervisory position that supports the food ingredients program unit team (PUT) within USP&rsquo;s Global Science and Standards Division (GSSD). The incumbent reports to a local management position at the India site as well as functionally reporting to a management position in the Foods PUT in the US. The incumbent will support the development and technical stewardship of Food Chemicals Codex (FCC) standards, other scientific products, outreach and awareness (in India, US, and internationally), and internal strategic initiatives. These activities require the ability to identify and critically evaluate published information on chemical analysis of food ingredients, regulatory and safety reviews of foods, and data and supplier documents to support development of standards and guidance documents. The successful candidate may develop proposals, coordinate, and lead specific technical studies related to food analysis. The incumbent may present technical talks to academics, the food industry, and regulators to advocate for the work of the program, to solicit feedback, and to support program goals related to awareness and capacity building. The incumbent will work collaboratively with industry stakeholders, the Food Ingredients Expert Committee, the PUT, and other USP program units and departments.
 
 
 
 How will YOU create impact here at USP?
 
 
 
 
 The Sr. Scientist I/II Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Provide scientific expertise to USP&rsquo;s Foods PUT with a focus on identifying, developing, and supporting food standards and other fit-for-purpose solutions.
 </li>
 <li>
 Perform critical evaluation of technical data related to food quality and purity including working closely with internal and external laboratories on analytical method development, validation, and data analysis.
 </li>
 <li>
 Works with USP staff, the USP Food Ingredient Expert Committee (FI EC), subcommittees (SC), and Expert panels (EP), external stakeholders as related to Food Ingredient monograph and RS development.
 </li>
 <li>
 Supports in the preparation of data packages and briefing materials to present to the FI EC and other expert bodies; manages projects appropriately and ensures impeccable work-product delivery.
 </li>
 <li>
 Foster collaboration and communication with other USP program units and departments,
 </li>
 <li>
 Keep abreast of global trends and developments in related scientific fields and share learnings with managers and colleagues.
 </li>
 <li>
 Communicate effectively with stakeholders from industry, academia, scientific organizations, and regulatory agencies.
 </li>
 <li>
 Assist and guide Expert Committees and related expert bodies to support the development of FCC standards and other program products.
 </li>
 <li>
 Performs other related duties in support of the Foods Program Unit as assigned.
 
 
 </li>
 </ul>
 
 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
 
 
 <ul>
 <li>
 Senior Scientist I: Ph.D. in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 7-10 years or MS in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 11-13 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted.
 </li>
 <li>
 Senior Scientist II: Ph.D. in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 10-13 years or MS in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 13-15 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted
 </li>
 <li>
 Candidates must have experience related to food safety, food quality, or analytical chemistry as well as outstanding written and verbal communication skills in English.
 </li>
 <li>
 Ability to review, analyze, and interpret and report on data from various analytical tests such as from HPLC, GC, LC/MS, GC/MS, IR, Raman, UV-Vis, NMR, ICP-MS, AA, etc.
 </li>
 <li>
 Experience in developing, validating, using, or evaluating food analytical methods
 </li>
 <li>
 Ability to communicate effectively and diplomatically with technical and non-technical stakeholders
 </li>
 <li>
 Experience in working directly in or with the food industry, such as experience with food quality systems, regulatory affairs, and supply chain management
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Ability to manage and prioritize multiple concurrent, complex projects with minimal direction and a history of successful timely project management
 </li>
 <li>
 Experience applying food regulations from local or international regulatory bodies, and collaborating with scientific standards organizations is a plus
 </li>
 <li>
 Ability to rapidly and expertly assess complex technical issues in a fast-paced environment
 </li>
 <li>
 Ability to embrace change. Adaptable, willing to learn, strong interpersonal and technical presentation skills; strong knowledge of MS Office and related products.
 </li>
 <li>
 Ability to operate independently where appropriate, yet understands when to escalate issues and how to establish effective working relationships
 </li>
 <li>
 Ability to work well with diverse employees and customers in a cooperative and friendly manner
 </li>
 <li>
 Able work flexible hours when needed
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 None, this is an individual contributor role.
 
 
 
 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.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Senior Scientist I /Senior Scientist II, Documentary Standards ( Foods)

<div>
 
 Description
 
 
 
 
 Who is USP?
 
 
 
 The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world&rsquo;s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide.
 
 
 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.
 
 
 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.
 
 
 
 Brief Job Overview
 
 
 
 This is a professional, highly technical, non-supervisory position that supports the Excipients program unit team (PUT) within USP&rsquo;s Global Science and Standards Division (GSSD). The incumbent reports to a local management position at the India site as well as functionally reporting to a management position in the Excipients PUT in the US. The incumbent will support the development and technical stewardship of NF standards, other scientific products, outreach and awareness (in India, US, and internationally), and internal strategic initiatives. Key responsibilities include support for the development of missing Excipient monographs and significant revision of the existing Excipient monographs and associated reference standards (RS) in the
 
 USP-NF
 
 that will contribute to USP&rsquo;s success for bridging the gap in introducing missing excipient monographs and keeping existing excipient monographs current. The incumbent will utilize his or her technical expertise, knowledge of excipient compendial monograph standard development process and current regulatory guidelines, and strong organizational and communication skills to ensure timely development of high-quality monographs and associated reference standards. The Science EXC PUT works closely with several other departments including Strategic Customer Development (SCD)/Standard Acquisition (SA), Compendial Operation, Global Laboratory Operations (GLO), Regions Program Operation (RPO) &ndash; Industry Program, and Global External Affairs (GEA).
 
 
 
 How will YOU create impact here at USP?
 
 
 
 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.
 
 
 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.
 
 
 
 The Senior Scientist I/II Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Works with USP staff, relevant USP Excipient Expert Committee(s) (EC), subcommittees (SC), and Expert panels (EP), external stakeholders as related to Excipient monograph and RS development.
 </li>
 <li>
 Supports in the preparation of data packages and briefing materials to present to the Excipients EC/SC/EP; manages projects appropriately and ensures impeccable work-product delivery.
 </li>
 <li>
 Participates in USP EC/SC/EP meetings, scientific conferences/meetings, outreach visits and other events sponsored by USP and/or pharmaceutical industry, trade associations, and regulatory agencies and provides supporting scientific expertise at EC/SC/EP meetings, internal and external meetings, scientific symposia, industry forums.
 </li>
 <li>
 Standard setting responsibilities include:
 </li>
 <li>
 Prepares data summary packages, briefing materials and other technical documents for correspondence with EC/CS/EP.
 </li>
 <li>
 Manages action items from monthly EC /SC/EP telecom meetings.
 </li>
 <li>
 Tracks and reports frequently on the status of assignments to management.
 </li>
 <li>
 Facilitates the accomplishment of key departmental metrics.
 </li>
 <li>
 Assists in writing manuscripts for publication by USP (e.g., PF proposals, stimuli articles) or in peer-reviewed journals.
 </li>
 <li>
 Applies knowledge of current trends in public health to prepare information for Expert Committee to facilitate decision-making.
 </li>
 <li>
 Performs other related duties in support of the Excipients &ndash;Science Program Unit as assigned.
 
 
 </li>
 </ul>
 
 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
 
 
 <ul>
 <li>
 Scientist I: Ph.D. in Organic Chemistry, Analytical Chemistry, Biochemistry or allied filed and 7-10 years or MS in Organic Chemistry, Analytical Chemistry or Biochemistry or allied field and 11-13 years, respectively, of relevant experience.
 </li>
 <li>
 Scientist II: Ph.D. in Organic Chemistry, Analytical Chemistry, Biochemistry or allied field and 10-13 years or MS in Organic Chemistry, Analytical Chemistry or Biochemistry or allied field and 13-15 years, respectively, of relevant experience.
 </li>
 <li>
 Candidates must have experience related to excipient composition, quality, or analytical chemistry as well as outstanding written and verbal communication skills in English.
 </li>
 <li>
 Ability to review, analyze, and interpret and report on data from various analytical tests such as from HPLC, GC, LC/MS, GC/MS, IR, Raman, UV-Vis, NMR, ICP-MS, AA, etc.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Should possess strong technical knowledge in the areas of complex molecules/compounds such as polymers, fats, oils, waxes and plants.
 </li>
 <li>
 Must be able to share technical information with non-technical or non-scientific staff, and to communicate effectively with representatives from pharmaceutical companies, government, and academic institutions. Ability to rapidly assess technical complications to identify, define, and solve technical issues
 </li>
 <li>
 Well-developed organizational, interpersonal communications, negotiation, writing, and strong listening and presentation skills.
 </li>
 <li>
 Proficient with pharmaceutical testing requirements and test protocols involving USP-NF compendial methods development for Excipient monographs.
 </li>
 <li>
 The ability to influence without direct authority.
 </li>
 <li>
 Results driven demonstrated with successful outcomes.
 </li>
 <li>
 Project Management skills and ability to prioritize tasks and manage multiple projects simultaneously.
 </li>
 <li>
 Able to operate independently where appropriate yet understands when to escalate issues and how to establish effective working relationships.
 </li>
 <li>
 Ability and desire to work well with diverse employees and customers in a cooperative and friendly manner.
 </li>
 <li>
 Ability to handle multiple priorities in a fast-paced environment.
 </li>
 <li>
 Able to work flexible hours when needed.
 </li>
 <li>
 Prior experience in a scientific based industry.
 </li>
 <li>
 Excellent written and verbal communications skills
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 None, this is an individual contributor role.
 
 
 
 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.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Sr Scientist I/ Sr. Scientist II, Documentary Standards (Excipients)

<div>
 
 Description
 
 
 
 
 Who is USP?
 
 
 
 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.
 
 
 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 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.
 
 
 
 Brief Job Overview
 
 
 
 This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent work collaboratively in the reference standard/ARM development program within the Global Biologics department. The incumbent will participate in the development of replacement and new reference standards /ARM in support of USP&rsquo;s mission and core business. The incumbent will also focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in timely manner.
 
 
 
 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 Sr. Scientist -I (RSS) Has The Following Responsibilities
 
 
 
 Roles and Responsibilities
 
 
 <ul>
 <li>
 Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies.
 </li>
 <li>
 Works to draft protocols, reports and address scientific and technical queries from internal and external stakeholders in timely manner pertaining to reference standards/ARMs
 </li>
 <li>
 Oversees and facilitates the development of standards and solutions to address analytical challenges associated with biological medicines.
 </li>
 <li>
 Supports day to day operations of the Stability (CSU) program covering the USP Biologics RS catalog inventory.
 </li>
 <li>
 Reviews RS testing history and drafts test protocols for collaborative studies and CSU studies and submits to labs based on designated testing requirements and schedules.
 </li>
 <li>
 Liaisons and Assists laboratories to ensure collaborative testing/CSU testing is completed accurately and in timely manner.
 </li>
 <li>
 Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use.
 </li>
 <li>
 Compiles current and historical Stability testing data assessment and prepare stability trend reports.
 </li>
 <li>
 Maintains and updates various databases documenting laboratory data and program determinations on suitability and Stability interval updates.
 </li>
 <li>
 Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Quality Assurance and Reference Standard Evaluation with investigation of unexpected stability testing results
 </li>
 <li>
 Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps.
 </li>
 <li>
 Prepare, present and discuss regular work updates with Team Lead and other team members
 </li>
 <li>
 Reviews protocols and/or reports of other Scientists as assigned by manager.
 
 
 </li>
 </ul>
 
 Who is USP Looking For?
 
 
 
 
 Preferred Qualifications
 
 
 
 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:
 
 
 <ul>
 <li>
 Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc.
 </li>
 <li>
 Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development.
 </li>
 <li>
 Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays.
 </li>
 <li>
 Excellent technical writing, presentation and oral communication skills are required.
 </li>
 <li>
 Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders.
 
 
 </li>
 </ul>
 
 Sr. Scientist I
 
 
 
 <ul>
 <li>
 Ph.D. degree in Biochemistry, Analytical Chemistry or Biological Sciences . Minimum of 7 to 10 years of post-educational work experience in recombinant therapeutic proteins, peptides and carbohydrates.
 </li>
 <li>
 in Biochemistry, or Biological Sciences with minimum of 11 to 13 years of commensurate industrial experience.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Knowledge of USP products and services is highly desirable.
 </li>
 <li>
 Operates collaboratively at all levels of the organization in a highly technical environment.
 </li>
 <li>
 Must be able to work in a fast-paced environment and respond to shifting priorities.
 </li>
 <li>
 Well-developed interpersonal, negotiation, conflict-resolution and listening skills.
 </li>
 <li>
 Must possess the ability to multi-task and to work effectively with a team.
 </li>
 <li>
 Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality.
 </li>
 <li>
 Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred.
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 No
 
 
 
 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.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Senior Scientist I, Documentary Standards(Biologics, Large Molecules)

<div>
 
 Description
 
 
 
 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 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.
 
 
 
 Brief Job Overview
 
 
 
 
 This is a hands-on, non-supervisory, non-laboratory role that serves as the liaison between the biopharmaceutical industry, regulatory agencies, USP departments and USP Expert Committees. The Documentary Standard Sr. Scientist facilitates the development of USP standards used by the global pharmaceutical industry. In this role, the incumbent will provide expertise, leadership, and guidance to USP Expert Committees and Expert Panels in the areas of mAbs, therapeutic proteins, peptides, oligonucleotides, antibiotics, gene therapy and vaccines, by facilitating the exchange of highly technical information and working collaboratively to improve and promote public health.
 
 
 
 <ul>
 <li>
 Identifies opportunities for new standards and solutions to address analytical challenges associated with the next generation of biological medicines.Develops strategies and processes for the elaboration of a steady pipeline of standards to support the analytical evaluation of different classes of biotherapeutics.
 </li>
 <li>
 Develops relationships with key stakeholders from academia, industry and regulatory communities to engage in collaborations in early pipeline development projects. Leads collaborations with academic and stakeholder groups.
 </li>
 <li>
 Collaborates with the biologics program unit team to gather insights based on internal and external data and perform analyses to inform on opportunities for further exploration. Communicates and maintains working relationships with other USP departments, as applicable.
 </li>
 <li>
 Plans and oversees necessary laboratory work for feasibility and proof of concept studies. Evaluates and analyzes scientific reports and identifies next steps and key challenges. Engages and builds relationships with internal and external laboratories to participate in round robin studies or in support of feasibility and proof of concept studies.
 </li>
 <li>
 Partners with the standards production team leads for eventual handoff leading to planning and initiation of standards development projects.
 </li>
 <li>
 Collaborates with internal groups to develop application notes, training materials, and online content to support standards.
 </li>
 <li>
 Leads expert panels and industry working groups; recruits and engages with members, defines project scope, and designs and advances work with input from external stakeholders and USP departments.
 </li>
 <li>
 Serves as representative of USP at professional scientific meetings organized by USP and other organizations. Gives public presentations on USP matters (as assigned).
 </li>
 <li>
 Stays ahead of current trends and developments in related scientific fields, particularly in the area of monoclonal antibodies and/or therapeutic proteins.
 
 
 </li>
 </ul>
 
 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
 
 
 <ul>
 <li>
 Ph. D. degree in Analytical Chemistry, Biochemistry, Biology, or a relevant field. A base of 7-10 years of relevant experience with bioanalytical development in the pharmaceutical industry.
 </li>
 <li>
 MS. level candidates with minimum of 11-13 years of commensurate industrial experience.
 </li>
 <li>
 Combination of fundamental work experience and education may be substituted
 </li>
 <li>
 Experience in process development, analytical characterization, and chemistry and manufacturing control (CMC) for biotherapeutics.,Strong experience in the areas of characterization and analysis of biopharmaceuticals,
 </li>
 <li>
 Experience in method development and characterization of biological products, impurities, and raw materials using a variety of physicochemical techniques and biological assays.
 </li>
 <li>
 Experience in method development, qualification and/or validation, method transfer, and development of system suitability criteria.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Knowledge of reference standards related to biopharmaceutical products/industry. Experience with reference materials manufacturing and development is a plus.
 </li>
 <li>
 Knowledge of national and international regulatory filings approaches. Familiarity with regulatory guidance documents from WHO, FDA, ICH and other international organizations.
 </li>
 <li>
 Demonstrated research, technical, and analytical skills, as well as the ability to take highly technical scientific information and make recommendations.
 </li>
 <li>
 Strong writing skills and experience drafting technical reports related to material characterization, method development and reference standard evaluation.
 </li>
 <li>
 Expertise in analytical methods applicable to biotherapeutics. Experience in analysis of proteins, peptides or oligonucleotides would be a plus. Experience in immunogenicity testing is also a plus.
 </li>
 <li>
 Demonstrated stakeholder collaboration experience, with the ability to develop and manage internal and external relationships and contacts.
 </li>
 <li>
 Ability to establish and nurture relationships with individuals of varying backgrounds and learning styles.
 </li>
 <li>
 Excellent presentation and communication skills (written and oral).
 </li>
 <li>
 Ability to communicate technical information with non-technical or non-scientific staff, and to interact effectively with representatives from pharmaceutical companies, government, and academic institutions.
 </li>
 <li>
 Project Management skills. Must have ability to prioritize and manage multiple, concurrent projects with often long-life cycles.
 </li>
 <li>
 Effective at operating independently where appropriate yet understands when to escalate issues and how to establish effective working relationships.
 </li>
 <li>
 Able to perform in a fast-paced environment with changing deadlines and priorities. Ability to manage and prioritize multiple, concurrent projects.
 </li>
 <li>
 Experience and knowledge of the USP-NF is preferred.
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 None, this is an individual contributor role.
 
 
 
 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.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Senior Scientist I, Documentary Standards (Pipeline Biologics)

Golden Opportunities

<div>
 
 Job Description
 
 
 
 Define, build, and lead a team of Data Scientists and Data analysts Discover areas in operations that can be automated through machine learning Demonstrate through technical knowledge on Statistical modeling, Probability and Decision theory, Operations Research techniques and other quantitative modeling techniques Understand the business reality behind large sets of data and develop meaningful solutions comprising of analytical solutions Work closely with internal stakeholders and align them with respect to your focus area Innovate by adapting new modeling techniques and procedures Implementing and operating stable, scalable data flow solutions from production systems into end-user facing applications/reports.
 
 
 
 Skills Required
 
 
 
 RoleData Scientist
 
 
 Industry TypeIT/ Computers - Software]
 
 
 Functional AreaIT-Software
 
 
 Required Education
 
 
 Employment TypeFull Time, Permanent
 
 
 Key Skills
 
 
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 DATA SCIENCE
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 MACHINE LEARNING
 
 
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 Other Information
 
 
 Job CodeGO/JC/1384/2025
 
 
 Recruiter NameRamya V
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Data Scientist - GO/JC/1384/2025

PepsiCo

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 Overview
 
 
 
 The Data Science Senior Analyst (Lead Data Scientist) is part of the Data Impact Benelux team. This team is responsible for supporting the Benelux commercial data strategy and ecosystem through developing and implementing advanced analytics solution and a comprehensive business intelligence roadmap. The team works closely with the marketing &amp; commercial ecosystem to ensure all commercial data are leveraged in the most optimal way.
 
 
 
 Responsibilities
 
 
 
 As the lead data scientist, this individual will be responsible for development and deployment of data science modeling frameworks using Statistical modeling (Machine Learning as appropriate) for sDNA and cDNA for BENLUX markets e.g., prediction of store potential, store segmentation, assortment optimization, asset deployment, audience profiling, etc.
 
 
 The position exists to unlock competitive advantage in go-to-market and execution through cutting edge data science, advanced analytics, and AI techniques, with a focus on OT, TT and AFH for BENLUX. The focus of this role is ensuring the successful implementation of data science solutions that deliver. The role holder will also leverage best practice to help to establish a reusable data science ecosystem.
 
 
 
 Qualifications
 
 
 
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 Bachelor's or advanced degree in a quantitative field for instance a Master&rsquo;s degree or PhD in data science or math (e.g., Computer Science, Mathematics, Statistics, Data Science) or equivalent experience
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 7 years + of relevant advanced analytics experience in Marketing or Commercial in either Retail, or CPG industries. Other B2C domains can be considered
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 Proven experience with medium to large size data science projects
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 Advanced knowledge of key data science techniques:
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 Combining data from multiple sources through APIs, Semantic Web, etc.
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 Data preparation and feature engineering
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 Supervised / Unsupervised learning
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 Collaborative Filtering
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 Location Analytics &amp; Intelligence
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 Proficiency in programming languages such as Python, R, or SQL.
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 Good to have experience with data processing frameworks (e.g., Hadoop, Spark)
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 Good to have understanding of data engineering principles, data integration, and ETL processes.
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 Excellent problem-solving skills and the ability to translate business needs into data-driven solutions.
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 Strong communication and interpersonal skills, with the ability to effectively convey complex concepts to both technical and non-technical stakeholders.
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 </ul>
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Sales Analyst

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