Registration Specialist: Herbicides, Ivm and Adjuvants

**Registration Specialist: Herbicides, IVM and Adjuvants - South Africa**:

- Job Id: 11355
- City: Durban, Gauteng, South Africa
- Department: Regulatory Operations
- Function: Regulatory Science & Government Affairs
- Employee Type: Permanent Full Time
- Seniority Level: Associate
- Description:

- **Job Title Registration Specialist: Herbicides, IVM & Adjuvants**

**Designation**Registration Specialist: Herbicides, IVM & Adjuvants

**Reporting To**Head of Regulatory, Southern Africa

**Skip Level Reporting**Regulatory Head, Africa

**Function**Regulatory

**GJL**GJL 3

**Location**Gauteng or KwaZulu-Natal

ABOUT UPL:

- UPL is focused on emerging as a premier global provider of total crop solutions designed to secure the world’s long-term food supply. Winning farmer's hearts across the globe, while leading the way with innovative products and services that make agriculture sustainable, UPL is the fastest-growing company in the industry. Our successes in the field add up to powerful financials. UPL delivers results from protecting crops that translate into attractive investor value. Based on the recognition that humankind is one community, UPL’s overarching commitment is to improve areas of its presence, workplace, and customer engagement._
- _
- Our purpose _is_ ‘OpenAg’. _An agriculture network that feeds sustainable growth for all._ No limits, no borders._
- We are one team, for maximum impact. One team with shared goals. We have a laser-like focus on what our customers need and want, on anticipating their future needs, and on how we can create innovative solutions and experiences for them. We think outside the box and go beyond our comfort zone. We believe in agility, we mix the power of speed, with structure from process. And wherever we can, we always believe in having fun._

Role Summary

Manage routine activities, including but not limited to, studying and compiling scientific and legal documents to ensure that products allocated to Herbicide, IVM and Adjuvant portfolio are in compliance with governmental regulations. Work in partnership with the Project Lead: Herbicides, Seed Treatment, Fumigants, Adjuvant & IVM on new project developments to ensure that all regulatory requirements are fully achieved to complement biological development in accordance with submission timelines and forecasted regulatory project budgets.

Role Responsibilities

**Regulatory**

1. Maintain the Herbicide portfolio under regulatory and legislative compliance within the geographic region under scope, i.e. South Africa (ZA)

2. Ensure registration of new products and maintain registrations of existing products within assigned portfolio/s within ZA.

3. Prepare, i.e. collect, evaluate (accuracy and integrity), organize, collate and maintain scientific, legal and regulatory information/data in a variety of formats, including but not limited to electronic databases and physical files, related to portfolio of products.

4. Ensure that the associated project regulatory expenses are paid on-time-in-full, in collaboration with R&D Administration Officer.

5. Report regularly (daily, weekly, monthly) on the status of products or projects and provide responses to questions/queries/correspondence to internal (management, other departments) and external stakeholders (headquarters, regulatory authorities) related to portfolio.

6. Work in Partnership and provide guidance to cross-functional teams such as Technical Product Development, Marketing and R&D PMO on regulatory requirements and the associated costs for submission of new business cases.

7. Liaise with Formulation Development for in-house product development and sample requirements for regulatory studies.

8. Ensure that suppliers of formulations and active ingredients meet the needs of ZA regulatory requirements.

9. Schedule and manage portfolio related product renewals on an annual basis.

10. Compile SDS's for new products and maintain updates for existing products.

11. Keep up to date with changes in regulatory legislation and guidelines and inform relevant internal and external stakeholders.

12. Ensure that quality standards are met and submissions meet strict deadlines.

13. Support ad hoc requests relating to regulatory functions and related company initiatives.

14. Support other regulatory Portfolios/New Portfolio/New Product Category (hybrid products) based on company need; seasonal workload, and company financial necessity.

15. Promote teamwork, communication and foster a knowledge sharing culture.

16. Be actively involved in all regulatory EDER (Early Detection, Early Resolution), activities, e.g. (including but not limited to) sudden changes in legislation such as implementation of GHS, or CMR molecules phase-outs. Provide early warning to business on regulatory trends, decisions, and possible impact.

17. Responsible for the compilation of high quality dossiers and/or submissions.

18. Create, modify and maintain operating procedures and processes pertaini