Regulatory Affairs Specialist

3 - 8 years

0 Lacs

Posted:1 day ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Job Title:

Senior Executive / Assistant Manager – Regulatory Affairs

Location:

Mumbai, India (On-site)

Employment Type:

Full-time | Permanent

Experience Required:

3 to 8 years

Industry:

Chemicals | Pharmaceuticals | Food & Beverages

Job Function:

Legal | Quality Assurance | Regulatory Affairs

Salary: up to 9 LPA


About the Role:

Senior Executive / Assistant Manager – Regulatory Affairs


Key Responsibilities:

  • Manage

    REACH registrations

    for new products across EU, Korea, Turkey, and UK, including tonnage upgrades and compliance letters.
  • Handle

    customer questionnaires

    and provide necessary

    declarations and certifications

    related to products and manufacturing sites.
  • Oversee renewal documentation for

    Halal, Kosher, FSSAI, RSPO, NSF

    , and other certifications.
  • Maintain

    water testing reports

    ,

    nutritional analysis

    , and manage

    FSSAI annual return filings

    .
  • Conduct

    internal audits

    under

    ISO 9001:2015

    as a certified internal auditor.
  • Address documentation requests from

    customers and logistics teams

    and resolve regulatory queries.
  • Regularly update company documents,

    certificates

    , and product declarations via

    OneDrive

    .
  • Train new team members on

    ISO standards

    ,

    documentation best practices

    , and

    REACH compliance

    .
  • Contribute to updating company website content (related to regulatory info and certifications).


Qualifications & Skills:

  • 3–8 years of experience in

    regulatory affairs

    ,

    compliance

    , or

    quality documentation

    .
  • Strong command over

    REACH

    ,

    ISO 9001:2015

    ,

    FSSAI

    , and international product certification processes.
  • Excellent

    written and verbal communication

    skills.
  • Strong attention to detail and

    documentation management

    skills.
  • Experience in

    chemical

    ,

    pharmaceutical

    , or

    FMCG

    industries is a plus.
  • Working knowledge of tools like

    MS Office

    ,

    cloud storage (OneDrive)

    , and

    online regulatory portals

    .
  • Why Join Us?

    • Work in a

      fast-growing and export-oriented

      chemical manufacturing company.
    • Gain exposure to

      global regulatory frameworks

      and international client documentation.
    • Be part of a

      compliance-driven, process-oriented culture

      .
    • Opportunity for career advancement within a growing regulatory department.

    How to Apply:

    Submit your updated resume. Shortlisted candidates will be contacted for further discussion.

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