About the role
Opening for one of MNC FMCG export company for the Scientific Associate / Sr. Scientific Associate
Roles:-
who will be responsible for ensuring compliance with local and international regulations governing the production, labelling, and distribution of our products. Also accountable for managing all aspects of regulatory affairs, including product registrations, submissions, compliance documentation, and communication with regulatory authorities.
CTC is upto 6 lakhs.
IV - DUTIES AND RESPONSIBILITIES
- Regulatory Strategy Development:
1.1. Develop and execute regulatory strategies to support the introduction of new products or variations to existing products.
1.2. Assess regulatory implications for changes in manufacturing processes and provide guidance to ensure ongoing compliance. Work closely with cross functional teams to support the premarket regulatory requirements, labelling requirements with the latest regulatory requirements.
- Government and Industry Relations
2.1 Represent the company in interactions with regulatory agencies, industry associations, and other relevant bodies.
2.2 Build positive relationships with regulatory authorities and participate in meetings, conferences, and seminars to stay abreast of industry trends.
- Interact with business stakeholders on Regulatory affair related projects, programs, issues and communications.
- Monitor regulatory changes, alert business on impacts and change management processes.
- Documentation and record keeping
5.1 Maintain comprehensive and accurate regulatory documentation, including product dossiers, technical files and correspondence with regulatory agencies.
X- LOCATION OF WORK
Cochin
IDENTIFICATION OF ALL REQUIRED SKILLS
1. Experience in handling regulatory affairs in Food/Spice/Seasoning/ Essential Oil/ Cosmetic/Nutra/Natural colours etc...
2. In-depth knowledge of local and international regulations pertaining to spice products, food additives, and food labeling.
3. Manage preparation and interpretation of Safety data sheets (SDS) as per GHS (EU CLP) in different languages
4. Manage REACH registration as per the EU REACH registration requirement.
5. Prepare the regulatory dossiers and submissions to customer and releasing relevant certificates to customers