Job Description

Company DescriptionAs a world market leader in crop protection,
we help farmers to counter these threats
and ensure enough safe, nutritious,
affordable food for all \xe2\x80\x93 while minimizing the
use of land and other agricultural inputs.
Syngenta Crop Protection keeps plants
safe from planting to harvesting. From the
moment a seed is planted through to
harvest, crops need to be protected from
weeds, insects and diseases
as well as droughts and floods, heat and
cold.
Syngenta Crop Protection is headquartered
in Switzerland.ROLE PURPOSE:Facilitation of Registration for crop protection products viz., Fungicides in India for high quality regulatory submissions in order to achieve registrations in a time bound manner.ACCOUNTABILITIES:

• To maintain regularly update , regulatory registration timelines and Regulatory intelligence for India.
• To update Veeva for Fungicides and other chemicals ( case to case basis)
• To generate data and prepare dossier on Chemistry , Bio-efficacy , residues. Toxicology , Packaging via study reports summaries on Pesticides
• MRL proformae on Pesticides for the purpose of submission to the regulatory authorities as per the submission timelines for India.
• To assist Head -Regulatory affairs in Industry issues / Crop Life matters
• To contribute in preparing deficiency replies to the regulatory authority, on assigned projects
• To prepare MRL proforma for submission to FSSAI for MRL setting
• To prepare dossiers for export registrations, RTT/ EUPs Label extensions, endorsement applications.
• Coordination with , Region , Global Reg managers
• Liaison with CROs for data generation of assigned regulatory projects
• To adhere with Syngenta\xe2\x80\x99s policies of regulatory compliance and work with honesty, dedication and positive attitude.
• To upload regulatory documents (CoR, Labels and Leaflets) in Veeva for concerned projects

QualificationsKNOWLEDGE SKILLS & EXPERIENCE:Critical Knowledge:

• Good understanding of generating data of crop protection products for registration purpose.
• Registration and regulatory data requirements .
• Good understanding of Pesticide registrations
• CP Regulatory guidelines of Indian regulatory framework
• EuPs, endorsement cases , export registrations, CIB data requirement / guidelines
• Bio stimulant regulatory frame work under FCO

Critical Skills:

• Good understanding of scientific writing and ability to prepare compelling technical arguments.
• Good verbal communication skills in English.
• Excellent organizational and analytical skills.
• Attention to detail and thoroughness, particularly under time pressure.
• Ability to work in a team and learn from team members.

Critical Experience:

• Maintaining database in consultation with regulatory collogues.
• Compilation of Regulatory dossiers.
• Export dossiers
• Label extension dossiers
• Digitization of regulatory records as per requirement.
• Good presentation development skills

Additional InformationPeople are at the heart of what we do:

• Once a year Full body check
• Competitive insurance scheme
• Employee assistance program \xe2\x80\x93 to take care of your and your loved ones mental health
• Paid Vacation of 30days, 12 Paid Holidays, Maternity and Paternity Leave, compassionate leaves
• Education assistance \xe2\x80\x93 for your career growth
• People first culture translated into \xe2\x80\x98Most Preferred place to work 2022-23 by Times group\xe2\x80\x99

Note: Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status.To learn more visit: andFollow us on: Twitter & LinkedIn

Syngenta