AdmissionNotice

Piramal Group Recruitment 2022-23 for Executive Regulatory Affairs Post in Mumbai

Full Time JOB SECTOR: Pharma Sector JOB SECTOR:-Health Sector OWNERSHIP:-Private
  • Full Time
  • JOB SECTOR: Pharma Sector
  • JOB SECTOR:-Health Sector
  • OWNERSHIP:-Private
  • Mumbai

Website Piramal Group

LAST DATE FOR APPLY: NOT DISCLOSED

Job Vacancy in Piramal Group

Application’s are Invited by Piramal Group, Pharma Job , Piramal Group has adopted a dual strategy of both organic and inorganic expansion during the course of its three decades of existence. Piramal Group persistently pursues inclusive growth while adhering to moral and values-based policies since it is driven by its core beliefs.

Interested and qualified applicants for the Executive Regulatory Affairs Post in MumbaiĀ who fulfilling the criteria may submit or apply their application according to the prescribed format along with the details CV as per Norms. For any query or full details visit their official websites https://www.piramal.com/

And If you are a fresher/experienced remember always a well-written application/resume would be of great value. Before you start to writing you application letter, at first know what the company is looking for and whether you are a right fit to the company culture or norms in the given below:

DATE OF JOB POST:

12/12/2022

NAME OF THE POST:

Executive Regulatory Affairs

LOCATION:

Mumbai

QUALIFICATION & EXPERIENCE:

Overall 2 to 5 work experience in managing Medical Regulatory affairs in Pharma / Consumer / OTC industry industry

Well versed with Regulations – DNC Act, DPCO, ASCI, UCPMP, FSSAI , Ayush

Communication & interpersonal skill

JOB DESCRIPTION:

Create a Medreg (Medical Regulatory) strategy and yearly operating plan, and put them into action.
Create monitoring systems to obtain information on medical and regulatory trends.
Analyze and share this data to aid in the development of corporate strategy.
Maintain communication with internal stakeholders to guarantee OTIF project delivery
Create procedures for exports and product registrations as necessary
establishing SOPs, specifications, success KRAs, and monitoring stakeholders’ adherence to medical regulatory standards

 

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