Regulatory Specialist
BASF
Objectives of the Position:
Provide support for the regulatory department to ensure efficient and compliant business processes and environment.Assist in the registration of products by preparing and submitting documentation needed for registration.
Main Tasks:
Administration Roles
Managing all stages of regulatory project from planning, executing, controlling and monitoring product registration process.Ensure all registration process including documents to be fully compliant.Keep relevant databases updated.
Operational Roles
Submit the necessary documents to Ministry of Agriculture via online submission as required.Monitor the clearances process of sample import and provide necessary administrative Regulatory relevant support.Ensure all registration trials running smoothly and finish on time.Ensure commercial label to follow current regulation from authorities, stewardship guideline and BASF AP labelling guideline.Support product stewardship implementation in the country.
Maintaining Relationship roles
Build an external relationship with the authorities and other relevant stakeholders within the company compliance guidance.Build networking to facilitate product registrations and acceptance of BASF products.
Regulatory and Advocacy roles
Provide information about the new regulation after announced.Represent the company in Industry association Regulatory task force activity.
Requirements:
Minimum bachelor’s degree in an agricultural or other related field.Minimum 4 years in the similar position.Knowledge in regulatory framework for pesticide registrationAbility to interpret regulatory requirements, analyse range of studies and extract relevant information for drafting of comprehensive dossier for submissionKnowledge in Regulatory Authorities, universities, research institute and other Regulatory relevant institutionsStrong communication skills (good in writing and speaking English).Computer literate. (good in using Ms. Word, Excel,).Good analytical thinkingAbility to periodically travel to visit trials or stakeholder engagement
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