Title: Principal / Senior Principal Scientist - Spectroscopy Location: Piscataway, NJ, US Department: Research & Development Job Description: Travel Required?: Travel - up to 10% of time Hybrid No Relocation Assistance Offered Job Number #173393 - Piscataway, New Jersey, United States Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name! Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values—Caring, Inclusive, and Courageous—we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all. As a Principal Scientist you will serve as a central technical resource supporting the entire global Colgate-Palmolive portfolio by developing and validating state-of-the-art analytical platforms to characterize complex product matrices. Operating within the global R&D organization, you will act as the technical arbiter of "Truth," ensuring that every chemical claim made by Marketing is backed by statistically rigorous, peer-reviewed-quality data. This role offers an exciting opportunity to spearhead Lab 4.0 digital transformations, run advanced competitive teardowns, and defend the company's intellectual property. Your primary objective will be to provide flawless analytical characterization that guarantees formulation parity, regulatory compliance, and consumer safety across all product categories. Responsibilities - Advanced Method Development: Designs and validates novel analytical protocols for active and critical inactive ingredients, stabilizers, and sensory molecules using high-resolution LC/GC MS and NMR technologies. - Crisis Chemistry & Forensic Analysis: Leads proactive monitoring and "Rapid Response" forensics for trace contaminants, conducting root-cause analysis on stability failures or manufacturing deviations to ensure safety amid supply chain shifts. - Deformulation & Competitive Intelligence: Conducts competitive product teardowns to break down rival formulations to their base molecules, utilizing non-targeted analysis (NTA) workflows to structurally identify unknown components, and evaluates optimized ingredients from new suppliers to ensure absolute formulation parity. - Claim Substantiation & Legal Defense: Partners with Marketing and Legal teams to transform analytical results into "Visual Science" for claim validation, ensuring all methods meet AOAC, USP, or ISO standards to remain legally unassailable. - Lab 4.0 & Digital Transformation: Evaluates high-throughput tools, oversees the implementation of MS Imaging platforms, and collaborates with Digital R&D to build automated data processing pipelines, feeding mass spec chemometric and big data into predictive Machine Learning models. - Sustainable Packaging Interface: Develops standardized methodologies including ultra-trace extractables and leachables (E&L) screening to investigate chemical interactions between formulas and new sustainable or recycled packaging materials to ensure zero migration of impurities. Required Qualifications - PhD in Analytical, Organic, or Medicinal Chemistry - 10 years of advanced laboratory experience. - Expert-level knowledge of High-Resolution LC-MS and GC-MS for content quantification and structure elucidation. - Technical proficiency in spectroscopic techniques including FTIR, Raman, and NMR as supporting tools for understanding molecular interactions within a formula. - Proven experience working within a GxP (GLP/GMP) regulated environment with a strong understanding of data "Chain of Custody" protocols. Preferred Qualifications - Specialized experience in Microbiome Analytics, including metabolomics or analyzing bacterial metabolites in complex biological samples. - Demonstrated background in "Green Chemistry" analytics, such as assessing the biodegradability of surfactants or the purity of post-consumer recycled packaging. - Strong collaborative capacity to translate complex analytical big data into actionable business strategies for cross-functional stakeholders. - Proven ability to support IP activities and patent filings by providing detailed molecular characterization data for new entities. Compensation and Benefits Salary Range $124,000.00 - $180,000.00 USD Pay is determined based on experience, qualifications, and location. Salaried employees may also be eligible for discretionary bonuses, profit-sharing, and long-term incentives for Executive-level roles. Benefits: Salaried employees enjoy a comprehensive benefits package, including medical, dental, vision, basic life insurance, paid parental leave, disability coverage, and participation in the 401(k) retirement plan with company matching contributions subject to eligibility requirements. Additional benefits include a minimum of 15 vacation/PTO days (hourly employees receive a minimum of 120 hours) and 13 paid holidays (vacation days are prorated based on the employee's hire date within the calendar year). Paid sick leave is adjusted based on role and location in accordance with local laws. Detailed information regarding paid sick leave entitlements will be provided to employees upon hiring and may be subject to adjustments based on changes in legislation or company policies. Our Commitment to Inclusion Our journey begins with our people—developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self, is treated with respect, and is empowered by leadership to contribute meaningfully to our business. Equal Opportunity Employer Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law. Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form should you require accommodation. For additional Colgate terms and conditions, please click here. #LI-Hybrid

Role Description Agile Decision Sciences LLC is looking for a Clinical Data Manager 4 to support our growing Center for International Blood & Marrow Transplant Research (CIBMTR) team. - Manage the delivery of high-quality data from project start-up and planning to project execution and project closeout on several projects. - Independently perform project specific quality control and quality assurance tasks on all projects. - Ensure consistency, accuracy, and adherence to federal regulations, Good Clinical Practice, Good Clinical Data Management Practices, as well as SOPs and Working Instructions. - Manage patient protocol information and review protocol, incorporating protocol-specific guidelines into the review of clinical trial data on several projects simultaneously. - Contribute to the design of the databases and forms, ensuring they meet requirements for entry and reporting of clinical data of varying complexity. - Test new processes and systems for the management of data in clinical trials. - Test clinical trial databases and data entry screens assuring compliance with protocol and institutional processes and procedures. - Process, track, and validate data accurately and on time, in accordance with data processing and entry instructions. - Perform data abstraction and data entry on several different protocols into multiple clinical research databases. - Develop and extract patient clinical data reports for publications and presentations. - Possess proficiency with clinical databases and report tools. - Identify project specific reports and assist in the development of these reports. - Prepare, review, and submit clinical data to monitoring agencies. - Maintain client communication regarding data management project status and review key project questions with clients. - Demonstrate a significant amount of initiative, autonomy, and proficiency in all areas above. - Train, mentor, and coach other clinical data managers. Qualifications - A bachelor’s degree. - 2-4 years of experience in a related or applicable field, or an equivalent combination of education and experience. Benefits - Competitive pay and benefits packages. - Health care, dental, vision, life insurance. - 401(k). - Education assistance. - Paid time off including PTO, holidays, and any other paid leave required by law. EEO Statement ASRC Federal and its Subsidiaries are Equal Opportunity employers. All qualified applicants will receive consideration for employment without regard to race, gender, color, age, sexual orientation, gender identification, national origin, religion, marital status, ancestry, citizenship, disability, protected veteran status, or any other factor prohibited by applicable law.

• SOSi is seeking a Data Governance & Metadata Scientist to support mission requirements for a structured approach to further develop, integrate, and sustain a scalable, federated data ecosystem that enhances interoperability, governance, and mission-driven analytics for a DoD customer. • The contractor shall establish and maintain metadata governance frameworks, ensuring compliance with DoD data management policies and interoperability with Data Catalog. • The contractor shall develop automated metadata tagging processes to improve data discoverability, classification, and lineage tracking within the Common Intelligence Picture (CIP) platform. • The contractor shall implement and manage data governance workflows, ensuring integration with OpenLineage, Unity Catalog, and GIS metadata standards. • The contractor shall submit the Metadata & Data Governance Compliance Report, detailing lineage tracking, classification policies, and security enhancements.

• Track database set-up, testing, maintenance and data entry • Communicate with clients, project teams and vendors on data management matters • Review study documents, design and develop project specific guidelines and instructions • Design eCRF, Data Management and Data Validation Plans and test EDC databases • Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation • Code medical data • Track and report metrics leading to database lock • Coordinate the processing, dispatch and archiving of CRFs/queries • Maintain Clinical Data Management working files • Perform database QC checks, prepare and attend audits • Train site staff and project teams on CRF completion and data management topics