Research Career @ Colgate-Palmolive | Associate Post for Pharma Candidates

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Colgate-Palmolive

Colgate-Palmolive is a leading global consumer products company, tightly focused on Oral Care, Personal Care, Home Care and Pet Nutrition. Colgate sells its products in over 200 countries and territories around the world under such internationally recognized brand names as Colgate, Palmolive, Speed Stick, Lady Speed Stick, Softsoap, Irish Spring, Protex, Sorriso, Kolynos, elmex, Tom’s of Maine, Sanex, Ajax, Axion, Fabuloso, Soupline and Suavitel, as well as Hill’s Science Diet, Hill’s Prescription Diet and Hill’s Ideal Balance.

Job Title:   Sr. ASSOCIATE – REGULATORY AFFAIRS

Job Description:  

  • Collaborate with Regulatory Affairs (RA) Managers on programs and activities within all regions to align on priorities and product registrations.
  • Manage RA Associates supporting roles by coordinating the efforts of the operational regulatory team based in India.
  • Manage global registration database and prepare documentation for registrations required for products manufactured in North America and distributed in other regions.
  • Support the regulatory strategy defined at Regional and/or Global level, and report regularly the progress to Regional RA Department with relevant KPIs, particularly in terms of timelines, status of supportive data required from other functions and dossier preparation.
  • Maintain and update the master registration tracking tool with existing, new and pending registration information.
  • Compile required documents from source countries for high quality and successful submissions, license renewals, annual registrations and maintenance of product registration dossiers for authorities.
  • Upload and publish electronic Common Technical Document (eCTD) sequences for drug and medicinal products for select regions.
  • Ensure Regulatory Assessments are completed in a timely manner.
  • Assist RA Regions with artwork approvals.
  • Manage preparation of core dossiers for multiple region filings to be modified for submission as needed at the regional level.
  • Ensure content, organization and overall quality of all regulatory documents and samples are adequate and complies with local/regional regulatory requirements, commitments and agreements.
  • Manage dossier and document storage for country registrations for easy reference.
  • Assist with artwork approval with regards to confirmation of INCI lists, registration numbers, review of product labeling and promotional material to ensure compliance with proof of claims.
  • Keep abreast of updates and changes with International Standards related to products and processes to ensure compliance. Provide feedback to country specific RA Managers

Qualifications:  

  • BS degree in Pharmacy or Life Sciences or relevant education.  Advanced degree preferred
  • At least 3-5 years of relevant experience in regulatory affairs, quality or product development in pharmaceutical, medical devices or similar FMCG/CPG companies.
  • Understanding of registration and regulatory requirements.
  • Knowledge of industry practices, techniques and standards.
  • Knowledge/understanding/experience in the following legislations and field would be an added value
  • Cosmetics/Home Care
  • Medical Devices/Medicinal Productss/Complimentary Medicine
  • Disinfectants

Application Instructions

Are you interested in working for Colgate-Palmolive? You can apply to work with us using this online application. Attach all relevant documents such as a cover letter and resume or CV. Applications received by e-mail are not considered in the selection process.

Become part of our team. We look forward to your application.

Equal Opportunity Employer
Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, or any other characteristic protected by law.

Apply Online

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