Job Title:  Associate Scientist

Relocation Assistance Offered Within Country
Job Number #165952 - Mumbai, Maharashtra, India

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.
 

Roles & Responsibilities

We are looking for (Sr.) Associate Scientist - Analytical Sciences to join our high-reaching team at our IGTeD center. The incumbent in this role will be responsible for end to end planning & implementation of planned analytical science initiatives in partnership with local & global analytical & product development teams for Oral care categories for India GTeD while being compliant to defined safety, quality & regulatory norms.

Key Responsibilities

• Coordinate with global R&D sites to provide end to end support for stability testing in partnership with global and local analytical and product development teams. 

• Perform testing and report the results of routine analysis, new product formats using Analytical Instrumentation in a cGMP environment.

• Transfer analytical methods and new technologies in consultation with the operational manager and provide analytical support and training for troubleshooting samples.

• Expertise in and proficient in the use of key analytical equipments - HPLC, GC, Ion Chromatography, other laboratory equipment

• Develop, optimize and validate analytical methods. Solve problems and apply troubleshooting to analytical instrumentation. Maintain, calibrate, qualify and troubleshoot instrumentation. Maintain accurate, up to date and concise laboratory records.

Key Stakeholders

Internal: I&S, Technical services, Supply chain, Quality/EHS,  Microbiology, manufacturing units and suppliers.

External: Global R&D, Manufacturing sites , analytical group & Quality Team.

Operational Excellence

• Demonstrate proficiency in knowledge in the identified scientific field. Keep tabs on the latest technical developments and breakthroughs by drawing on industry contacts, scientific literature, conferences, and patent filings. Build on technical expertise, growing it in complementary directions. Use technical expertise and creativity to proactively identify potential problems and address them using appropriate resources.

• Share internal and external technical knowledge discoveries, ideas, and vision with colleagues through documentation, presentations, publications, and patents.

• Drive initiatives to simplify and improve technical processes. Translate technical attributes into simple, Use statistical approaches to experimental design to increase learning with the least amount of time and with minimum resources.

• Be 100% compliant to all Product Safety, Quality and Regulatory requirements to operate with cost efficiency and speed. Practice good documentation practices and ALCOA+ principles. 

Qualification & Requirements

• Able to handle assigned business programs independently with minimum supervision.

•  Should be able to give & seek feedback on an   on-going basis by using Colgate’s mentor program and initiatives

• M.Sc.(Analytical Science, Bioanalystical, Organic Chemistry or similar qualification)/ Masters in Pharmacy 

• Solid understanding and expertise in chromatography (HPLC/GC) and proficient with Openlab software, compliance to 21 CFR Part11 for Electronic records (Chromatography operating software) 

• Worked as analytical scientist with a large multinational pharma/FMCG organization with experience in stability testing

• Minimum 2 years of experience, in which min 1 yr. of experience must be a direct hand on HPLC/GC in a cGMP environment

• Support analytical method validation, required degradation studies, prepare method validation documentation and report generation

• Maintaining knowledge of current testing methods as applicable to stability studies, knowledge of ICH/WHO/FDA guidelines and cGMP requirements, ALCOA+ principles and stability testing is a must.

• Detailed knowledge of eLN and LIMS will be an added advantage

• Technology Fundamental, Technology Innovation, Product Safety, Regulatory and Quality, Execution Perfection, Analysis & Decision Making, Problem Solving and Business Presentation skills

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Our Commitment to Diversity, Equity & Inclusion
Achieving our purpose starts with our people — ensuring our workforce represents the people and communities we serve —and creating an environment where our people feel they belong; where we can be our authentic selves, feel treated with respect and have the support of leadership to impact the business in a meaningful way.

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.

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