Executive Registration
2 days ago
**Executive Registration**:
- Job Id: 4445- City: Bangalore, Karnataka, India- Department: Research and Development- Function: Regulatory, Research and Development- Employee Type: Permanent Full Time- Seniority Level: Executive- Description:
- **About UPL**
**UPL is a leader in global food systems and with the acquisition of Arysta LifeScience, is now one of the top 5 agricultural solutions companies worldwide. With revenue of US$5 billion, UPL has presence in 130 countries. With market access to 90 percent of world’s food basket and focused on high-growth regions, UPL represents a compelling value proposition for growers, distributors, suppliers and innovation partners in a consolidating market. UPL offers an integrated portfolio of both patented and post-patent agricultural solutions for various arable and specialty crops, including biological, crop protection, seed treatment and post-harvest solutions covering the entire crop value chain.**
**Purpose of the Role**:
- Regulatory support for registration of Bio-solution products, globally
- Handle entire gamut of registration in assigned countries/region
- Study/data sponsoring & monitoring - in-house and externally (research centres/CRO’s)
**Responsibilities**:
Timely co-ordination with R&D scientists, Analytical teams, QA, Mfg. & SCM teams to generate and support regulatory/product technology documentations and product samples
Assist to sponsor and monitor studies (lab & field) at GLP CRO’s/Labs/Field Institutes for their timely availability
Responsible to handle entire gamut of registrations in assigned region in co-ordination with regional regulatory teams
Co-ordination with region to understand and develop regulatory frame-work to register bio-solution products (rules, regulations, data requirement, guidelines, process, time and cost required)
Timely attend registration deficiencies and renewal of registrations in assigned country/region
Keep track and monitor of regulatory field studies conducted in-house & at CRO’s/Res. Institutes
Provide technical support to region to register bio-solution products
Work closely with all other internal key functions & outside customers for creating regulatory, safety documents for assigned regulatory portfolio.
Handle data evaluation, data gap and investment analysis for new products and existing products for geographical expansion.
Regulatory budget creation for assigned region in co-ordination with region and its monitoring
Close co-ordination with NPPL portfolio/marketing to generate regulatory capexes and fast track their approvals
Management of CRO invoices and payment
Create regulatory data Masters related to assigned region/country and its time to time updation.
Maintain all regulatory records related to assigned territory
- Close co-ordination with IPD/IPR teams for FTO clearance
- Project Life cycle Management in assigned region
- If required, should travel to HO, in field, countries/region for regulatory work
**Qualification**:
- M.Sc (Agri) Pl. Pathology/Entomology/Agronomy, MSc in Biological sciences
- 2-4 years of relevant experience
- Knowledge about Agro biopesticide / biological iindustry, Regulatory norms & documentations
**We are all about connecting with people, in a human way - showing respect, demonstrating trust, celebrating diversity. For us technology is an enabler, not the endgame. We see the value in human connectivity and how it creates new opportunities for everyone. With this, comes our promise to protect people’s safety in every way we can.
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