Regulatory Documentation

5 days ago

Mumbai Central Mumbai Maharashtra, India A A ATTARWALA & GROUP Full time

Job Summary:
regulatory requirements and documentation, specifically in the fragrance industry. The successful

Sheets (SDS), IFRA (International Fragrance Association) allergen reports, and related documents for

queries and provide efficient solutions to support the business.

**Responsibilities**:

- Access and manage regulatory documentation, including SDS, IFRA allergen reports, CLP

(Classification, Labeling, and Packaging), EU GHS, and non-animal testing reports for aroma
- Provide accurate and timely information to internal stakeholders regarding regulatory

requirements, updates, and changes.
- Develop and maintain knowledge of IFRA, EU, and CLP regulations, as well as emerging

regulatory trends in the fragrance industry.
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements for

fragrance products.
- Develop and maintain a comprehensive understanding of fragrance safety assessments,

including skin irritation and sensitization testing.
- Independently answer queries related to regulatory documentation and compliance, providing

solutions to support the business.
- Maintain accurate records, reports, and databases of regulatory documentation and

compliance.
- Develop and maintain relationships with internal stakeholders to ensure regulatory

requirements are met.
- Perform other related tasks as assigned by management.

**Requirements**:

- Education: Bachelor's degree in Life Sciences, Regulatory Affairs, or a related field.
- Experience: 2-3 years of experience in regulatory affairs, specifically in the fragrance industry.
- Knowledge:

- IFRA (International Fragrance Association) guidelines and regulations.
- EU GHS (Global Harmonization System) and CLP (Classification, Labeling, and Packaging).
- Non-animal testing methods and regulations.
- Basic laws and regulations governing fragrances and aroma ingredients, including REACH

(Registration, Evaluation, Authorization, and Restriction of Chemicals) and biocides

directives.
- Safety Data Sheets (SDS) and allergen labeling compliance.
- Familiarity with electronic databases and document management systems, including

SDS databases and online platforms for fragrance safety assessments.

**Skills**:

- Excellent communication, analytical, and problem-solving skills.
- Strong organizational and time management skills, with the ability to prioritize tasks and meet

deadlines.

and Google Drive.
- Ability to work independently, with mínimal supervision, and as part of a team.
- Strong attention to detail, with the ability to maintain accurate records and reports.

Working Conditions:

- This role requires a strong computer-based working environment, with the ability to work

independently and communicate effectively with internal stakeholders.

Note:
This job description is not an exhaustive list of all responsibilities, duties, or requirements. The company

reserves the right to make changes to this job description as necessary.

**Job Types**: Full-time, Permanent

Pay: ₹30,000.00 - ₹40,000.00 per month

**Benefits**:

- Health insurance

Work Location: In person

  • Regulatory Documents Assistant

    13 hours ago

    Mumbai, India Innovaderm Research Full time

    The Regulatory Documents Assistant will establish and maintain the Sponsor electronic or paper Trial Master File (TMF) throughout the life of the trial, and will perform record review of essential documents for accuracy and quality according to ICH-GCP. The Regulatory Documents Assistant is also responsible for the set-up of the Investigator’s Study File...

  • Regulatory Affairs Executive

    2 weeks ago

    Mumbai, Maharashtra, India R. Wadiwala Sec Pvt Ltd Full time

    Designation : Regulatory Affairs Specialist - Qualifications : Bachelor's degree in a scientific discipline, such as pharmacy, biology, or chemistry - Experience : Minimum 2-5 years of experience in regulatory affairs - Salary : Good Hike on Current CTC - Location : Sandhurst Road Mumbai - Head

  • Expert Regulatory Writer

    2 weeks ago

    Mumbai, Maharashtra, India Novartis Full time

    393319BR **Expert Regulatory Writer**: India **About the role** Position Title: Expert Regulatory Writer About the role: Expert Regulatory Writer Location - Hyderabad #LI Hybrid The number of regulatory documents we authored last year. As an Expert Regulatory Writer, you will develop documents which cover all Novartis therapeutic areas and therapies,...

  • Regulatory Affairs Officer

    1 week ago

    Mumbai, Maharashtra, India MEDVARSITY ONLINE LIMITED Full time

    Job Title: Senior Executive - Regulatory Affairs UK/IE/MT Department: Regulatory Affairs Grade Level: P-2 Reports to: Manager / Sr. Manager - Regulatory Affairs Number of Reports: NONE Location: Mumbai **Main purpose of role**: To ensure adequate and prompt life cycle maintenance activities for Marketing Authorization’s (MA) held based on portfolio...

  • Regulatory Affairs Associate

    2 weeks ago

    Mumbai, Maharashtra, India Planet Science Full time

    **About Us**: An established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform **- CLYZO** **Position - Regulatory Affairs Associate.** An organization with a reputed history of 10+ years in the Pharma raw material industry, dealing in excipient products is looking for Regulatory Affair Executive having...

  • Regulatory Manager

    2 weeks ago

    Mumbai, Maharashtra, India Adani Realty Full time

    Job DescriptionResponsibilities- Develop and implement regulatory strategies to ensure compliance with all applicable laws and regulations in the construction industry- Monitor and evaluate regulatory requirements for construction projects and provide guidance to project teams- Coordinate with internal teams, external consultants, and regulatory authorities...

  • Associate, Regulatory Affairs

    2 weeks ago

    Mumbai, Maharashtra, India Colgate-Palmolive Full time

    Relocation Assistance Offered Within Country Job Number #163733 - Mumbai, Maharashtra, India **Who We Are** Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the...

  • Am- Regulatory Affairs-international

    1 week ago

    Mumbai, Maharashtra, India Domnic Lewis Pvt. Ltd Full time

    **AM- Regulatory Affairs-International**: **Domnic Lewis has been Mandated to hire for AM- Regulatory Affairs-International** **Function / Department**: Regulatory Affairs - International Markets **Direct Reports**: None **Primary Purpose of the Role**: To ensure the timely preparation, review, and submission of high-quality regulatory dossiers for...

  • Coordinator, Regulatory Submissions

    1 week ago

    Mumbai, Maharashtra, India Fortrea Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Regulatory Affairs Executive

    7 days ago

    Mumbai, Maharashtra, India Clini launch Business Solutions Full time

    We are seeking a knowledgeable and experienced Regulatory Affairs Specialist with expertise in the Drugs & Cosmetics Act and FSSAI regulations, as well as experience in FDA-related activities. This role is essential for ensuring robust functional and cross-functional coordination (R&D, QC, Marketing, Legal, Production, etc.) and for the transparent execution...