Sr Manager CP Regulatory

4 weeks ago

new delhi, India Syngenta Crop Protection Full time
Job Description

ROLE PURPOSE

  • Liaisoning with regulatory authorities (CIB&RC, CIL, ICAR , FSSAI , INM etc) for all regulatory submissions and follow up . Important role in developing Regulatory strategy.
  • Focal point for toxicology. Develop tox dossier, reply tox queries and other tox related regulatory challenges / issues.
  • Key role in Crop Life Task Force viz., Toxicology TF , Biostimulant/ Biologicals  etc.
  • Accountable for quality dossier submission to regulatory authorities of India ,  to ensure quality data generation from 3rd party CROs , Govt Universities /ICAR Institutes etc  , meeting registration guidelines , in order to achieve registrations in a time bound manner.    
  • Effective Product defence as FTO/LTO operations for product  Life cycle management

ACCOUNTABILITIES

  • To obtain registrations in time bound manner from CIB&RC.
  • To have a clear understanding and sound knowledge of regulatory and registration guidelines as stipulated from authorities and keep on evolving ,for registering crop protection / Household/ Public Health  products in India.   
  • To coordinate and liaise with CROs via continuous follow-ups and obtain quality reports for timely registering crop protection products in India.
  • Liaison with INM  authorities for Bio-stimulant , Biofertilizers etc registrations
  • To develop scientifically sound reply to the query of regulators after dossier submission.
  • To liaise with Regional  / Global stake holders in Syngenta  for various inputs for dossier and while replying to queries of authorities.   
  • Coordination with ICAR for comments / Peer opinion before granting registration.
  • National MRLs – interaction and follow up  with Food Safety & Standards Authority of India (FSSAI, MoH&FW).
  • Support in Crop Life Activities (via Member of Core group/ Task Force )
  • To adhere with company’s business aspirations by achieving milestones and timelines in a cost effective, efficient and cooperative manner.
  • To adhere with Syngenta’s policy of regulatory compliance and work with honesty, dedication and positive attitude.

 

 


Qualifications

4.  KNOWLEDGE SKILLS & EXPERIENCE

Critical Knowledge:

  • Ph.D. / M.Sc. in Agri. Sciences or allied sciences
  • Good understanding of generating Tox, bio-efficacy , residue data , chemistry data generation of crop protection and House Hold / Public Health products
  • Registration and regulatory requirements of India
  • IT literacy

Critical Skills:

  • Good scientific writing and ability to prepare compelling technical arguments
  • Excellent verbal communication skills in English
  • Excellent organizational and analytical skills
  • Attention to detail and thoroughness, particularly under time pressure
  • Ability to lead a small team

Critical Experience:

  • In-depth working knowledge of crop protection products (herbicides, insecticides, fungicides, plant growth regulators, bio-pesticides, Biostimulants , House Hold and Public Health ( known as SPS in Syngenta)
  • Good track record of Advocacy with  Regulatory authorities in CIB&RC , FSSAI, ICAR , CIL , INM and scientists of government institutions (SAUs / ICAR)
  • Regulatory experience of 12 -15 years in Crop Protection products registrations

Critical Skills:

  • Proactive attitude and a strong motivation towards working in time bound manner
  • Ability to use computers and to work disciplined with database management
  • Ability to work in a multicultural, de-centralized and multifunctional team
  • Ability/willingness to travel regionally and occasionally globally
  • High attention to detail and consistency in performance
  • Good planner but also a good stress manager. Basic understanding of project management and planning.
  • Ambition to grow in the job and in the company
  • Ability to Communicate effectively (verbal and written) in English

SYNGENTA CORE DIMENSIONS

  • Results Oriented
  • Team Oriented
  • Decisive
  • Communicative and open
  • Customer-Focused
  • Innovative
  • Disciplined

Level:  Professional

Other Behaviors Critical for the role :

  • Willingness to work as per deadlines
  • Flexibility and willingness to travel as required
  • Strong stewardship outlook, as part of approach to gaining registrations
  • A good interpersonal skill is a must

CRITICAL SUCCESS FACTORS AND KEY CHALLENGES

  • Number of registrations obtained
  • Number of molecules defended
  • Good experience of  liaising with Indian regulatory authorities , Govt. officers
  • Proven track record in obtaining new molecule registration by curbing regulatory challenges
  • Rich knowledge / Regulatory sense of precedents of various approvals from CIB&RC
  • Proven  contribution in  developing Regulatory strategy and assessing registrability

WORKING CONDITIONS / PHYSICAL DEMANDS

PHYSICAL DEMANDS OF THE ESSENTIAL FUNCTIONS:

  • Physically fit to work and to stay focused under pressure

WORKING CONDITIONS WHILE PERFORMING ESSENTIAL FUNCTIONS:

  • Domestic and international travel possible with overnight stays. 
  • Person  must  be  fully  conversant  with  (and willing to learn) the  existing regulatory environment, rules and regulations and the evolving regulatory environment

 


Additional Information
  • Once a year Full body check
  • Competitive insurance scheme
  • Employee assistance program – 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 – for your career growth
  • People first culture translated into ‘Most Preferred place to work 2022-23 by Times group’

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: 

Follow us on: Twitter & LinkedIn

  • Twitter
  • LinkedIn

  • Sr Manager CP Regulatory

    2 weeks ago

    New Delhi, India Syngenta Crop Protection Full time

    Job DescriptionROLE PURPOSELiaisoning with regulatory authorities (CIB&RC, CIL, ICAR , FSSAI , INM etc) for all regulatory submissions and follow up . Important role in developing Regulatory strategy.Focal point for toxicology. Develop tox dossier, reply tox queries and other tox related regulatory challenges / issues.Key role in Crop Life Task Force viz.,...

  • Sr Manager CP Regulatory

    1 month ago

    New Delhi, India Syngenta Crop Protection Full time

    Job DescriptionROLE PURPOSELiaisoning with regulatory authorities (CIB&RC, CIL, ICAR , FSSAI , INM etc) for all regulatory submissions and follow up . Important role in developing Regulatory strategy. Focal point for toxicology. Develop tox dossier, reply tox queries and other tox related regulatory challenges / issues. Key role in Crop Life Task Force viz.,...

  • Assistant Manager

    1 month ago

    New Delhi, India Syngenta Crop Protection Full time

    Job DescriptionROLE 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...

  • Sr Manager CP Regulatory

    2 weeks ago

    Delhi, Delhi, India Syngenta Crop Protection Full time

    Job DescriptionROLE PURPOSE Liaisoning with regulatory authorities (CIB&RC, CIL, ICAR , FSSAI , INM etc) for all regulatory submissions and follow up . Important role in developing Regulatory strategy. Focal point for toxicology. Develop tox dossier, reply tox queries and other tox related regulatory challenges / issues. Key role in Crop Life Task Force...

  • Sr Manager CP Regulatory

    2 weeks ago

    Delhi, Delhi, India Syngenta Crop Protection Full time

    Job DescriptionROLE PURPOSELiaisoning with regulatory authorities (CIB&RC, CIL, ICAR , FSSAI , INM etc) for all regulatory submissions and follow up . Important role in developing Regulatory strategy. Focal point for toxicology. Develop tox dossier, reply tox queries and other tox related regulatory challenges / issues. Key role in Crop Life Task Force viz.,...

  • Academic Coordinator Delhi Cp

    4 weeks ago

    New Delhi, India IMS Proschool Full time

    **Position: Academic Coordinator/ Student Outcome** **Location: New Delhi CP** **Job Role** The job involves managing the entire back end operations viz. servicing students enrolled for various courses of the company. The job entails - Managing the entire post admission/ enrolment process and activities. - Faculty/Trainer Coordination and networking and...

  • Academic Coordinator Delhi Cp

    4 weeks ago

    New Delhi, India IMS Proschool Full time

    **Position: Academic Coordinator/ Student Outcome** **Location: New Delhi CP (Near Janpath Metro)** **Job Role** The job involves managing the entire back end operations viz. servicing students enrolled for various courses of the company. The job entails - Managing the entire post admission/ enrolment process and activities. - Faculty/Trainer Coordination...

  • SR Manager Medical Device- Regulatory Affairs

    2 weeks ago

    Delhi, India Zoot Systems Full time

    Zoot Systems is a New Delhi India based company. For years it has been ourcontinuous endeavours to understand Client qualityconsciousdiscerning business needs and to successfully meet those. Wespecialize in the creation of highquality I.T./NonI.T. based HRSolutions Recruitment and RPO to companies of all sizes resultingin better faster and more meaningful...

  • Regulatory Affairs Specialist

    4 days ago

    Delhi, India Meril Full time

    We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices Domain to join our team. Positions are: Executive / Sr. Executive / Asst. Manager Regulatory Affairs Experience: 3 to 9 years Location: Andheri east, Mumbai Working Days: 6 days (Mon-Sat) WFO Responsibilities: 1. Dossier collation...

  • Regulatory Affairs Specialist

    2 weeks ago

    Delhi, Delhi, India Meril Full time

    We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices Domain to join our team.Positions are: Executive / Sr. Executive / Asst. Manager - Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) - WFOResponsibilities:1. Dossier collation and...

  • Regulatory Affairs Specialist

    4 weeks ago

    Delhi, India Meril Full time

    We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices Domain to join our team.Positions are: Executive / Sr. Executive / Asst. Manager - Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) - WFOResponsibilities:1. Dossier collation and...

  • Regulatory Affairs Executive

    4 weeks ago

    Delhi, Delhi, India Ample Leap Cognition & Technologies Pvt Ltd Full time

    DESIGNATION/ TITLE Sr. Executive / Assistant Manager - Regulatory Affairs LOCATION NSP, Delhi YEAR OF EXP Minimum 3 yrs QUALIFICATION MSc (Toxicology/Agri/Chem) or similar BUDGET In b/w 8-10Lpa KEY RESPONSIBILITIES ROLES & RESPONSIBILITIES Manage the data gathering and compilation of studies (toxicology, chemical, efficacy) necessary for the...

  • Manager - Regulatory Affairs - Medical Devices

    4 days ago

    New Delhi, India DSS Imagetech Pvt Ltd Full time

    About Position:This is a full-time on-site position for a Regulatory Affairs Manager in New Delhi. The Regulatory Affairs Manager will be responsible for managing the Regulatory Affairs function of the organization and it's group companies and communicating effectively with internal & external stakeholders. QualificationsDegree in BPharm / MPharm / Biotech...

  • Manager - Regulatory Affairs - Medical Devices

    2 days ago

    New Delhi, India DSS Imagetech Pvt Ltd Full time

    About Position:This is a full-time on-site position for a Regulatory Affairs Manager in New Delhi. The Regulatory Affairs Manager will be responsible for managing the Regulatory Affairs function of the organization and it's group companies and communicating effectively with internal & external stakeholders. QualificationsDegree in BPharm / MPharm / Biotech...

  • Regulatory Affairs Executive

    3 weeks ago

    New Delhi, India Euronoxx Reserves ltd Full time

    **Regulatory Affairs Manager** **Benefits** JOB TYPE: Permanent EMPLOYMENT TYPE: Full-Time EXPERTISE: PHARMACEUTICAL REGULATORY AFFAIRS SALARY TYPE: Annually SALARY: Negotiable REPORTS TO: Managing Director VACATION LEAVE: paid LOCATION: Shimla, Himachal Pradesh, India. This role will be office-based or hybrid **REQUIRED: Direct experience working...

  • Manager/Lead - Regulatory Affairs - Pharmaceutical Firm

    4 weeks ago

    New Delhi, India Domnic Lewis International Full time

    We are looking for a Lead Regulatory Affairs who is specialized in Indian market regulatory affairs with good connections in DCGI for a Global Pharmaceutical MNC in Delhi / BangaloreJob Description:We are looking for a Regulatory Affairs Lead to lead regulatory processes for our assigned products, ensuring swift approvals and strict compliance with...

  • Regulatory Reporting

    1 week ago

    Delhi, India Kotak Mahindra Bank Full time

    Department: Wholesale Banking (Credit Monitoring) Grade: Manager/ Sr. Manager Experience: Minimum 3 years experience in Regulatory Reporting. Qualification: CA/MBA Job Description: PAN Bank Exposure report and CRILC return : Preparing the PAN Bank Exposure Report. Co-ordinating with various department of the bank to get the data / information for PAN Bank...

  • Manager -Taxation

    1 week ago

    New Delhi, India Aces Global Consulting Pvt Ltd Full time

    Manager - TaxationLocation = CP New DelhiCTC = 18 Lac to 20 LacQualifications: Qualified CAsNote : Candidates from CA firm will only be cconsidered.Who will direct and manage multiple operations related to taxes and deliver tax services.Your primary responsibility is to manage specific tax-related functions like advisory, litigation, appeals and assessments...

  • Agm - Regulatory

    1 month ago

    New Delhi, India Vodafone Idea Full time

    Job Req ID: 41743- Location: New Delhi, IN- Function: Technology/ IOT/Cloud- About: - Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India’s leading telecom service provider. The Company provides pan India Voice and Data services across 2G, 3G and 4G platform. With the large spectrum portfolio to support the growing...

  • Sr. RA Specialist

    1 week ago

    new delhi, India Danaher Full time

    The Sr. Specialist Regulatory Affairs will independently, with minimum supervision, initiate and prepare the regulatory submissions, interact with Business Units Regulatory affairs teams and interact with regulatory agencies/health authorities to obtain and maintain product approvals with a focus on India, Sri Lanka and other SWA Countries, as per the...