Mô tả công việc
Purpose:
Responsible for the timely registration of new products of the Business group and the renewal of registration of current products.
Regularly visit the regulatory authorities and report on any development that may affect the business and are responsible for updating all Bayer Consumer Health's regulatory databases.
Scope (global, regional or local):
• Conducts technical review and assessment, prepares and submits to the regulatory authorities all pertinent documents related to product registration.
• Secures from Global Regulatory Affairs, other Bayer affiliates & from R&D the required documents and materials needed for ensuring local registrations.
• Provides regulatory support and guidance to colleagues in their procurement, marketing, sales and manufacturing activities to ensure compliance to relevant internal and external regulations.
• Assists marketing in development and documentation of product claims, text and promotional materials to comply with HA regulations.
• Develop and foster personal contact within HA and other pertinent agencies.
• Conducts competitive intelligence networking of products as necessary. Conducts training on relevant SOPs, Issues and laws, product information as necessary.
• Attend to queries related to product information.
Key Tasks:
1. Maintain registration of products intended for local marketing.
2. Coordinates requirements from governmental agencies concerned for product initial registration/renewal and documentation.
3. Fulfills medical and pharmaceutical certification, clearance of reclassification, promotional approval requirements requested by Marketing.
4. Reviews text of local product inserts (PIs), local Artwork in coordination with the internal approvers, consistent with agreed task ownership matrices.
5. Develops objectives and strategies on tasks to ensure implementation and successful achievement of all plans.
6. Formulates together with line manager, individual performance objectives to enhance expertise, technical skills and overall effectiveness.
7. Ensures maintenance and upkeep of all regulatory affairs documents
and internal reporting databases.
8. Performs other duties required by line manager from time to time.
Yêu cầu
• Have medical or pharmaceutical background with a minimum of 1 years experience in the field of Regulatory Affairs.
• Fluent in English and local language(s)
• A team player
• Strategic thinker and good analytical skills
• Good interpersonal and communication skills
• A high level of attention to detail
Quyền lợi
Thưởng
• Private Health Insurance
Chăm sóc sức khoẻ
• Other Benefits as company policies
Khác
• Work From Home Policy
Thông tin khác
NGÀY ĐĂNG
23/09/2026
CẤP BẬC
Nhân viên
NGÀNH NGHỀ
Y Tế/Chăm Sóc Sức Khoẻ > Dược Sĩ
KỸ NĂNG
Regulatory Affairs, Product Registration, Regulatory Compliance, Pharmaceutical QC, Medical
LĨNH VỰC
Dược phẩm
NGÔN NGỮ TRÌNH BÀY HỒ SƠ
Bất kỳ
SỐ NĂM KINH NGHIỆM TỐI THIỂU
1
QUỐC TỊCH
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