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Sr. Analytical Scientist

Job in Trumbull, Fairfield County, Connecticut, 06611, USA
Listing for: Unilever
Full Time position
Listed on 2026-02-15
Job specializations:
  • Science
    Research Scientist, Data Scientist
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Sr. Analytical Scientist page is loaded## Sr. Analytical Scientist locations:
Trumbull, CTtime type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
February 26, 2026 (13 days left to apply) job requisition :
R-1174937
** OUR BUSINESS
** Established in 2018, Unilever’s US-centric Wellbeing Collective business is a collective of fast-growing, science-backed companies powering a lifestyle of wellbeing designed for a lifetime of possibilities. Comprised of Liquid I.V., Nutrafol, OLLY, Onnit, Smarty Pants, Welly and Equilibra (in Italy), the Wellbeing Collective operates with a start-up mindset and is supporting consumers on their proactive wellbeing journey by bringing innovative products to the market.  

Unilever identified Wellbeing Collective as a key growth space for the future and has built the business through a clear M&A criteria and growth strategy to €1bn+ turnover, delivering double-digit, volume-led growth quarter after quarter.  You will be part of the Global team which is responsible for launching WBC’s brands across the world. This cross functional team has end to end responsibility for international expansion of the brands in a fast-paced environment.

If you are excited. about the prospect of bringing disruptive brands across the world this role is for you    
** JOB DESCRIPTION OVERVIEW
** Analytical Scientist, in the R&D setting will be responsible for leading Analytical work streams for operating companies within WBC category. The role will have heavy interactions and coordination across cross functional teams in operating companies - product development team, quality, regulatory and external contract labs to ensure timely delivery of the objectives.

** KEY

ACCOUNTABILITIES
** Collaborate with operating companies to support with following analytical method related work streams to:
* Collaborate with contract laboratories to outsource analytical method development and validation activities for active ingredients such as botanicals and chemical markers in complex matrices, leveraging industry trends to identify new markers.
* Develop protocols or scopes of work for method development, validation, verification, and troubleshooting, ensuring alignment with industry and Wellbeing Business Category (WBC) standards and guidelines as necessary for matrix optimization.
* Review relevant formulation inputs and apply validated scientific methodologies across all phases of the study.
* Oversee the life cycle and operational aspects of analytical methods, including logistics, study initiation, sample management, testing, data analysis, reporting, invoicing, study closure, and sample disposal.
* Analyze method validation data to inform conclusions, address matrix-specific challenges through troubleshooting, and lead method optimization using systematic gap analysis.
* Design and conduct analytical investigations, providing root cause analysis as needed.
* Support calculations for product formulation, specifications, and research and development requirements.
* Facilitate analysis of FP, in-process and raw material samples for various products and matrices, including investigational support.
* Ensure timely execution of key project deliverables, and accurate recording, reporting, and interpretation of data related to method development, validation, and transfer for new products—such as gummies, soft gels, capsules, powders, tablets, or liquids—within the Wellbeing category.
* Assist in resolving analytical challenges within the business, supporting investigations of out-of-specification or trending results as required. Maintain comprehensive documentation of all collected data, establishing and adhering to analytical documentation practices.
* When needed support for Stability study workflows along with formulators or basis different projects requirements.
* Comply with Good Manufacturing Practices (GMP), Safety, Health, and Environmental (SHE) requirements, and all applicable regulations. Complete assigned SHE is training in a timely manner, perform daily tasks according to global SHE policies, report any observed unsafe acts or conditions, and participate in designated safety-related processes and…
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