Regulatory Affairs Intern

4 days ago

Prahlad Nagar Ahmedabad Gujarat, India Maven Profcon Services LLP Full time

Job Description:
As a **Medical Device Regulatory Affairs Intern**, you will work alongside experienced regulatory professionals, gaining hands-on experience in regulatory submissions, compliance research, and documentation for medical devices.

Key Responsibilities:

- Assist in preparing regulatory documentation for product registrations and submissions.
- Conduct research on international medical device regulations (EU MDR, US FDA, etc.).
- Support the compilation and maintenance of technical files and regulatory reports.
- Review and update regulatory compliance databases.
- Assist in writing and editing regulatory documents, reports, and summaries.
- Coordinate with cross-functional teams to gather necessary regulatory information.
- Monitor regulatory changes and updates to ensure compliance.

**Requirements**:

- Currently pursuing or recently completed a degree in Biomedical Engineering,Biotechnology or Regulatory Affairs, or a related field.
- Strong interest in medical device regulatory affairs and compliance.
- Excellent research and analytical skills.
- Strong written and verbal communication skills.
- Attention to detail and ability to manage multiple tasks.

**Job Type**: Internship
Contract length: 6 months

Pay: ₹5,000.00 - ₹8,000.00 per month

Schedule:

- Day shift

Ability to commute/relocate:

- Prahlad Nagar, Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (required)

Work Location: In person

  • Regulatory Affairs Executive

    6 days ago

    Ahmedabad, Gujarat, India vital group Full time

    **Job Opening: Regulatory Affairs Executive | Vital Group** Location: SG Highway, Ahmedabad **Experience**: 1-3 years (Pharma Industry) **Key Responsibilities**: - Preparation and submission of dossiers, CTD/ACTD, and regulatory documents. - Handling regulatory queries and compliance requirements. - Coordination with internal teams to ensure timely...

  • Regulatory Affairs

    2 weeks ago

    Ahmedabad, India Maven Profcon Services Full time

    **Experience**: 0 - 5 Yrs. **Qualification**: MS-Regulatory affairs, Diploma in Regulatory Affairs, M Pharmacy, B.E Biomedical engineering, M.sc Biotechnology, M.sc Microbiology & graduation/post-graduation in any related scientific discipline **Job Profile**: As a Regulatory Affairs executive, you shall: - Prepare technical documentation for various...

  • Regulatory Affairs Executive

    18 hours ago

    Ahmedabad, India Prime Placement Full time

    Position: Regulatory Affairs Assistant - Cosmetic Industry Department: Regulatory Affairs Experience Required: 0-2 years Location: Santej, Ahmedabad Salary Range: 2.2 LPA - 3 LPA Roles & Responsibilities: 1. Handling Legal Documents and Regulatory Affairs: - Assist in the preparation, review, and submission of regulatory documents. - Maintain and...

  • Regulatory Affairs Executive

    1 week ago

    Sola, Ahmedabad, Gujarat, India DF Pharmacy Full time

    **Job Role: Regulatory Affairs (RA) Head (Male preferred)** **Responsibilities**: - Oversee regulatory submissions, compliance, and approvals for products. - Ensure adherence to international and local regulatory requirements. - Develop and implement regulatory strategies to support business objectives. - Lead communication with regulatory authorities and...

  • Regulatory Affairs Executive

    2 days ago

    Jagatpur, Ahmedabad, Gujarat, India Pharmaceutical Distributor Full time

    **Introduction**: We are seeking a Regulatory Affairs Executive to join our team. In this role, you will be responsible for getting new products approval from the regulated market. In-depth knowledge of US FDA, EMA, and ICH regulatory frameworks, eCTD/ACTD dossier preparation, compilation and submission. Familiar with regulatory tools like Extedo, Lorenz,...

  • Regulatory Affairs Executive

    7 days ago

    Navrangpura, Ahmedabad, Gujarat, India Bexcode Services Full time

    **Regulatory Affairs Executive Job Description** **Job Summary**: The Regulatory Affairs Executive will work with product development and manufacturing management to ensure that the product development process meets all applicable regulatory requirements. **Duties/Responsibilities**: - Works in the regulatory affairs department on assigned projects. -...

  • Regulatory Affairs Executive

    2 weeks ago

    Ahmedabad, Gujarat, India WEST-COAST PHARMACEUTICAL WORKS LTD Full time

    **Job Title**: Regulatory Affairs Executive **Department**: Regulatory Affairs (RA) **Location**: Sola, Ahmedabad **Job Summary**: **Key Responsibilities**: - **Preparation and Compilation**: - Prepare registration dossiers in CTD, ACTD, or country-specific formats as per regulatory requirements. - Arrange and organize registration documents according...

  • Regulatory Affairs Executive

    6 days ago

    Ahmedabad, Gujarat, India SUNTARA COSMETICS Full time

    **Responsibilities** - Review formulations and claims and provide regulatory guidance to ensure full compliance to regulations including mandatory standards. - Oversight of the preparation and filing of regulatory documents with the FDA and international regulatory bodies; setting the standards for and reviewing all submissions to assure adequacy and...

  • Regulatory Affairs Executive

    3 days ago

    Ahmedabad, Gujarat, India Vital Group Full time ₹ 12,000 - ₹ 14,90,645 per year

    Job Opening: Regulatory Affairs Executive | Vital GroupLocation: SG Highway, AhmedabadExperience: 1–3 years (Pharma Industry)Key Responsibilities:Preparation and submission of dossiers, CTD/ACTD, and regulatory documents.Handling regulatory queries and compliance requirements.Coordination with internal teams to ensure timely submissions.Support in product...

  • International Regulatory Affairs Manager-Ahmedabad

    3 days ago

    Ahmedabad, Gujarat, India Claps Industries Full time US$ 60,000 - US$ 1,20,000 per year

    We are hiring an International Regulatory Affairs Executive/Manager with expertise in regulatory documentation, CTD dossiers & query handling. Immediate joiners preferred. Candidates with 1+ year experience may also apply. Join our growing team