Colgate-Palmolive Released Work From Home Job Opportunity For Pharmacy or Life Science Grduates

Colgate-Palmolive Released Job Openings On 24/05/2022.Colgate-Palmolive Company is an American multinational consumer products company headquartered in Park Avenue, Midtown Manhattan, New York City. It specializes in the production, distribution and allocation of household, health care, personal care and veterinary products.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Colgate-Palmolive s Group Recruitment 2021 are provided below. Interested and eligible candidates can  submit application along with resume. 

Vacancy Details:

Colgate-Palmolive Recruiting BS degree in Pharmacy or Life Sciences or relevant education. Advanced degree preferred with Minimum 1-3 yrs. of experience for Associate – Regulatory Affairs Position.Complete Details for the Associate – Regulatory Affairs as follows.

Important Details :

• Location :Mumbai(Remote working option during the current situation)
• No of Vacancies:Not Disclosed by Recruiter
• Details of Salary:Not Disclosed by Recruiter
• Opening date for online Application: 24/05/2022
• Mode of application :Online
  
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

Related Job :Alkem Laboratories Walk-In On 29th May 2022 For B.Pharma,M.Pharma,12th,ITI,Diploma- Unable To Attend Walk In Mail Resume 

For more Latest pharma jobs https://pharmajobscooin.wordpress.com/

Job Description/Skills Required

• 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 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, 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 labeling and promotional material to ensure compliance with proof of claims.

Click here for Official notification and Apply