BPharmacy Jobs in Regulatory Affairs at Colgate-Palmolive
Colgate-Palmolive is seeking a skilled Regulatory Associate in Mumbai, Maharashtra, to support product registrations, regulatory compliance, and life-cycle management for a diverse portfolio spanning cosmetics, medical devices, home care, and medicinal products. This role offers an opportunity to work with a global leader trusted in over 200 countries, ensuring products meet regulatory standards while contributing to a healthier future.
- Job Position: Regulatory Associate
- Location: Mumbai, Maharashtra, India
- Job ID: #168693
About the Company
Colgate-Palmolive is a global leader in consumer products, operating in over 200 countries with renowned brands in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Guided by values of Caring, Inclusivity, and Courage, the company is dedicated to building a healthier future for people, pets, and the planet.
Job Description
The Regulatory Associate will assist with regulatory affairs activities for the India Extended Hub, managing product registrations, ensuring compliance, and supporting life-cycle maintenance for cosmetics, medical devices, home care products, medicinal products, and other categories. Reporting to the Regulatory Affairs Lead, this role involves executing regulatory strategies, preparing submissions, maintaining product dossiers, and ensuring compliance with local and global standards.
Key Responsibilities
- Support regulatory affairs programs for new product registrations and life-cycle management.
- Assist in implementing regional/global regulatory strategies and reporting progress with KPIs.
- Compile documents for submissions, renewals, and maintenance of product registration dossiers.
- Prepare and submit regulatory applications to authorities for timely approvals.
- Maintain product registration archives, ingredient databases, and tracking tools.
- Assist in preparing SOPs and ensure document archiving for compliance purposes.
- Review and approve product artwork as required.
- Stay updated on relevant regulatory guidelines and developments.
- Collaborate with the Regulatory Operations team for the timely execution of tasks.
- Contribute to regulatory training plans and participate in key regulatory meetings.
Qualifications
Required:
- Bachelor’s degree in Pharmacy, Life Sciences, or equivalent.
- Minimum 3 years’ experience in regulatory affairs, quality, or product development in pharma, medical devices, FMCG, or CPG sectors.
- Knowledge of registration and regulatory requirements in India, as well as familiarity with other hub countries, is a plus.
- Proficiency with databases, eCTD software, MS Office, Google Suite, SAP, and regulatory portals.
Preferred:
- Strong communication, planning, and organizational skills.
- Fluency in English.
- Experience with medicinal products and medical devices.
