Colgate-Palmolive Life Sciences Associate Job In Regulatory Affairs
Colgate-Palmolive Life Sciences Associate Job In Regulatory Affairs. BSc or MSc Life Sciences Jobs. Interested and eligible applicants can check out all of the details on the same below
Name of the Post – Associate – Regulatory Affairs
Travel Required? – No Travel
Date – May 22, 2022
Remote working option during the current situation
Relocation Assistance Offered Within Country
# 134782 – Mumbai, Maharashtra, India
Summary –
- This position will handle and maintain product compliance during the whole life cycle, for any category of products, specifically for products marketed in the USA and Canada. This position will report to the Team Lead, Regulatory Operations.
Key Responsibilities –
- Work closely with and support the Regional Regulatory Affairs Department in new product registration and life-cycle management of CP portfolio, including but not limited to, product renewals, variations, notifications and/or new license applications.
- Support the regulatory strategy defined at the Regional and/or Global level, and report regularly the progress to the Regional Regulatory Affairs Department with relevant important metrics, particularly in terms of timelines, the status of encouraging data required from other functions and dossier preparation.
- Compile documents and information required for high quality and successful submissions, license renewals and annual registrations, and maintenance of product registration dossiers for Authorities and Notified Bodies.
- Provide support for State and EPA registrations per US requirements, Drug and Device annual establishment registrations, and Voluntary Cosmetic Registration Program activities.
- Assist in the preparation of Regulatory Standard Operation Procedures, and in keeping track of revision dates.
- Assist in preparing core dossiers for multiple region filings to be modified for submission as needed at the regional level.
- Forward regulatory bundle to the country authority or external consultant/external lab/ partnership (where applicable).
- Update and maintain product registration and ingredients archives, databases and tracking tools.
- Assist with artwork approval with regards to confirmation of INCI lists, registration numbers, review of product labelling and promotional material to ensure compliance with proof of claims.
- Stay ahead of updates and changes with International Standards related to products and processes to ensure compliance.
Requirements –
- BS degree in Pharmacy or Life Sciences or relevant education. Advanced degree preferred.
- At least 1-3 years of validated experience in regulatory affairs, quality or product development in the pharmaceutical, medical devices or similar FMCG industries.
- Understanding of registration and regulatory requirements in the USA (federal and state) and Canada.
- Knowledge of industry practices, techniques and standards.
- Excellent digital literacy, which includes working with Google Suite, electronic databases, eCTD software, MS Office applications, Adobe Acrobat Standard or Professional, SAP, DMS, and Authority Regulatory databases and portals for handling changes and submissions.
- Good written and verbal communicator with excellent interpersonal skills.
- Good planning and organizing skills.
- Good excellent teammate and collaborative.
- Ability to work under tight deadlines and meet timelines.
- Proficiency in spoken and written English is mandatory.
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