Sarvotham Care Freshers | Regulatory Affairs Executive -apply Now

Sarvotham Care

Sarvotham Care Freshers | Regulatory Affairs Executive -apply Now

Sarvotham Care Freshers | Regulatory Affairs Executive -apply Now

Sarvotham Group is a leading Contract Development and Manufacturing Organization (CDMO) in India, serving the healthcare industry since 1982. The company specializes in nutraceuticals, probiotics, over-the-counter pharmaceuticals, and herbal formulations. Sarvotham Care emphasizes research and development and operates state-of-the-art manufacturing facilities in Baddi, Himachal Pradesh (SEZ), and Suchitra, Hyderabad, ensuring world-class production processes for its multinational clientele.

Application Link

Position Name : Regulatory Affairs Executive

Organization : Sarvotham Care

Qualification: B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Experience: 0 YEARS / Freshers – 1 Year

Salary: 25,000 – 35,000 /month

Location:  Hyderabad, Telangana, India

As a Regulatory Affairs Executive at Sarvotham Care, you will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, and preparing dossiers. You will handle various aspects of regulatory affairs to ensure that healthcare products meet all necessary regulatory standards.

Qualifications

  • Skills: Regulatory Documentation, Regulatory Requirements, Regulatory Compliance, Dossier Preparation, Regulatory Affairs expertise
  • Soft Skills: Attention to detail, strong analytical skills, excellent communication and collaboration skills, ability to work in a fast-paced and dynamic environment
  • Knowledge: Familiarity with FDA regulations and guidelines
  • Experience: Previous experience in the healthcare industry is a plus
  • Education: Bachelor’s degree in Pharmaceutical Sciences or a related field
  • Application Link

Are You a Good Fit for This Job?

To determine your fit for this role, consider the following:

  1. Experience: Do you have experience in regulatory documentation, compliance, and dossier preparation?
  2. Education: Do you hold a Bachelor’s degree in Pharmaceutical Sciences or a related field?
  3. Skills: Are you familiar with FDA regulations and guidelines, and do you have strong analytical and communication skills?

Positioning Yourself for the Job

  1. Highlight Relevant Experience: Emphasize your experience in regulatory documentation, compliance, and dossier preparation. Provide specific examples of projects or tasks you have managed successfully.
  2. Showcase Analytical Skills: Demonstrate your attention to detail and analytical capabilities through examples of how you ensured compliance and met regulatory requirements in your previous roles.
  3. Emphasize Collaboration: Highlight your ability to work in a team and collaborate effectively with cross-functional teams to meet regulatory standards.

Application Link

https://chat.whatsapp.com/DO9PMPj2H3K4SikyHri52x

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This Post Has One Comment

  1. Brahmanapalle pooja

    I am good fit for this role. I have 2 years experience in regulatory affairs.
    Skills :
    1. Dossiers preparation for ROW countries ( like Moldova ,srilanka,Cambodia,Iran,…..etc)
    2. Preparation of CTD ,eCTD
    3. Review of MFRs
    4. Review of specification,test methods of finished products
    5. Handling of chance controls and QMS
    6. Handling of regulatory documents
    7. Retrieval and archival of the documents..etc

Comments are closed.