Regulatory Affairs Manager (Ahmedabad)

Regulatory Affairs Manager (Ahmedabad)

02 Aug
|
SUNTARA COSMETICS
|
Ahmedabad

02 Aug

SUNTARA COSMETICS

Ahmedabad

Job responsibilities

- Well versed with all Regulatory operational standards and procedures and regulatory compliance for the product labels country wise.
- Very good knowledge in international regulatory requirements for US FDA, EU, ASIAN, MIDDLE EAST countries.
- Knowledge and understanding of regulatory compliance procedures of personal care products.
- Being able to prepare various certificates such as COA (Certificate of Analysis), MSDS, QQF, Certificate of No Animal Testing, Certificate of GMP, Certificate of Impurities,
- Free Sales Certificates as per Customer’s requirement.
- Knowledge on customer complaint handling. Well versed in checking the label, text and artworks as per the EU, US FDA, ASIAN, GSO regulatory requirements.
- Studying Legal Documents and collating information in a variety of formats.
- Ensuring compliance with regulations set by the Cosmetics &
- Perfumes Regulatory Agency as per country wise requirements.
- Keeping up to date with changes in regulatory legislation and guidelines
- Outlining requirements for labelling, storage and packaging. Maintain product drawing/Artworks/ documents distribution record.
- Maintain the MSDS, QQF which are required for the customer’s country wise.
- Responsibilities include record keeping, all documents such as specification procedures, inspection schedule and records to QC/QA procedures.
- Preparation of Specification for In-Process, Intermediate, Raw material (RM), Packaging material (PM) testing as per regulatory requirement.
- Preparation of Test Data Sheet for Intermediate, Raw material, Packaging material &
- Stability Testing.
- To review and prepare Impact Assessment / Risk Assessment report.




- Maintain and support procedures to ensure the compliance of all cosmetic products and packaging.
- Gather and maintain data for raw materials and production batches ensuring GMP and customer compliance.
- Prepare accurate, complete documentation in a timely manner as necessary.
- Preparation of product specifications.
- Receiving and getting approval of the final art works for their color text, legal requirements as per the customers’ / Country wise regulatory requirement.
- Updating the legal requirements and checking the art works as per the legal requirements for the various countries / customers.
- Preparation of the various certificates like COA, certificate of no animal testing, certificate of GMP, certificate of impurities, free sale certificate as per the customer’s requirement.
- To constantly engage researching new regulation updates and should be able to take pro-active action with respect to the updating of the formulation,
- Artwork and labelling for non- compliant products.

Skills &

Competencies Required

- Must have a thorough knowledge of the regulatory documentation requirements for the personal care industry.
- Should be well versed with US FDA, EU regulatory requirements.
- Should be well versed in the preparation of MSDS, COA, PIF and CPNP files.
- Very positive knowledge on Indian Drug &
- Cosmetic manufacturing Act especially on Schedule S Standards &
- GMP.
- User knowledge in JD Edwards / MS windows.
- Problem Solving.

Result

Orientation

- Environmental monitoring. Knowledge of Calibration of Instruments. Documentation and reporting
- Knowledge of Cosmetic RM/ PM stability Tests. Analytical and attention to details

📌 Regulatory Affairs Manager (Ahmedabad)
🏢 SUNTARA COSMETICS
📍 Ahmedabad

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