Regulatory Affairs ManagerCông ty TNHH Zuellig Pharma Việt Nam
Ngành nghề: Y tế - Dược, Pháp luật/ Pháp lý
Lương: Thỏa thuận
Hình thức: Toàn thời gian
Ngày đăng: 16/05/2024
Hạn nộp: 16/06/2024
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Mô tả công việc
ABOUT ZUELLIG PHARMA
Zuellig Pharma (ZP) is one of the largest healthcare services groups in Asia and our purpose is to make healthcare more accessible.
For past 100 years, we have been the trusted partner for healthcare companies looking to realize opportunities in Asian markets. With our deep-reaching infrastructure and sole focus on healthcare, we offer our clients unparalleled access to all healthcare channels across 13 countries in the region. Our focus is always about combining our market insight with a thorough understanding of your needs to deliver the best solution that connects you to patients. We believe delivering your products is only the first step to capturing the Asian markets. That is why we have continued to invest in developing innovative solutions that expand across Logistics, Clinical Reach, Sales & Marketing, Patient Centered Services, and Community Pharmacies.
ZP THERAPEUTICS
Beside Logistics service, Zuellig Pharma group also provide commercial solution to our clients under business unit: ZP Therapeutics. ZP Therapeutics is the partner of choice for companies looking for a sales and marketing partner in Asia. With offices in 13 markets across Asia and over 2,500 associates, our commercial excellence, in-market capabilities and strong ethical principles have driven the group's success as a trusted partner for the healthcare industry.
Purpose of Position
- To manage product registrations in line with MOH regulation
- Manage one Regulatory Affairs Executive at least
Responsibilities
- Develop, maintain and update the processes for product registration, trademark and license changes
- Manage preparation, submission and follow of initial and renewal product registrations, variations
- Review and approve labels in relation to the regulatory compliance
- Coordinate, provide, review the registered product information of principals on requirement of other functions like marketing, tender, importation ,..
- Coordinate and provide regulatory guidance in pharma fields to the team, other functions and principals. Proactively analyze, comment and communicate any changes in the regulatory environment.
- Develop and maintain the working network with MOH, associations and relevant organizations to carry out drug registration, cosmetic, medical device
- Support the Regulatory Affairs Team to ensure high quality of registration dossier and following with the local authority. Effectively manage and accelerate registration approval.
- Other tasks as assigned
Zuellig Pharma (ZP) is one of the largest healthcare services groups in Asia and our purpose is to make healthcare more accessible.
For past 100 years, we have been the trusted partner for healthcare companies looking to realize opportunities in Asian markets. With our deep-reaching infrastructure and sole focus on healthcare, we offer our clients unparalleled access to all healthcare channels across 13 countries in the region. Our focus is always about combining our market insight with a thorough understanding of your needs to deliver the best solution that connects you to patients. We believe delivering your products is only the first step to capturing the Asian markets. That is why we have continued to invest in developing innovative solutions that expand across Logistics, Clinical Reach, Sales & Marketing, Patient Centered Services, and Community Pharmacies.
ZP THERAPEUTICS
Beside Logistics service, Zuellig Pharma group also provide commercial solution to our clients under business unit: ZP Therapeutics. ZP Therapeutics is the partner of choice for companies looking for a sales and marketing partner in Asia. With offices in 13 markets across Asia and over 2,500 associates, our commercial excellence, in-market capabilities and strong ethical principles have driven the group's success as a trusted partner for the healthcare industry.
Purpose of Position
- To manage product registrations in line with MOH regulation
- Manage one Regulatory Affairs Executive at least
Responsibilities
- Develop, maintain and update the processes for product registration, trademark and license changes
- Manage preparation, submission and follow of initial and renewal product registrations, variations
- Review and approve labels in relation to the regulatory compliance
- Coordinate, provide, review the registered product information of principals on requirement of other functions like marketing, tender, importation ,..
- Coordinate and provide regulatory guidance in pharma fields to the team, other functions and principals. Proactively analyze, comment and communicate any changes in the regulatory environment.
- Develop and maintain the working network with MOH, associations and relevant organizations to carry out drug registration, cosmetic, medical device
- Support the Regulatory Affairs Team to ensure high quality of registration dossier and following with the local authority. Effectively manage and accelerate registration approval.
- Other tasks as assigned
Yêu cầu
Education & Qualification
- University degree
- Licensed Pharmacist
Working Experience
- 05 years experience working with multinational companies involved in product registration
Skill
- Must have good written and oral communication skills in English and Vietnamese and present him/her to principals and HCP with confidence and composure
Other Specific Requirements
- Good personality
- Planning and organizational skills
- Open and independent mind and attitude
- Good listener and team player
- University degree
- Licensed Pharmacist
Working Experience
- 05 years experience working with multinational companies involved in product registration
Skill
- Must have good written and oral communication skills in English and Vietnamese and present him/her to principals and HCP with confidence and composure
Other Specific Requirements
- Good personality
- Planning and organizational skills
- Open and independent mind and attitude
- Good listener and team player
Quyền lợi
Thưởng
13th month salary and performance bonus
Chăm sóc sức khoẻ
health insurance for you and your children
Nghỉ phép có lương
18 days of annual leave
13th month salary and performance bonus
Chăm sóc sức khoẻ
health insurance for you and your children
Nghỉ phép có lương
18 days of annual leave
Thông tin khác
NGÀY ĐĂNG
16/05/2024
CẤP BẬC
Trưởng phòng
NGÀNH NGHỀ
Dược > Phân Phối Dược Phẩm
KỸ NĂNG
Regulatory Affair, Product Registration, Pharmacy, Pharmaceutical Healthcare, English Communication
LĨNH VỰC
Dịch vụ Y tế/Chăm sóc sức khỏe
NGÔN NGỮ TRÌNH BÀY HỒ SƠ
Tiếng Anh
SỐ NĂM KINH NGHIỆM TỐI THIỂU
5
QUỐC TỊCH
Không hiển thị
Xem thêm
16/05/2024
CẤP BẬC
Trưởng phòng
NGÀNH NGHỀ
Dược > Phân Phối Dược Phẩm
KỸ NĂNG
Regulatory Affair, Product Registration, Pharmacy, Pharmaceutical Healthcare, English Communication
LĨNH VỰC
Dịch vụ Y tế/Chăm sóc sức khỏe
NGÔN NGỮ TRÌNH BÀY HỒ SƠ
Tiếng Anh
SỐ NĂM KINH NGHIỆM TỐI THIỂU
5
QUỐC TỊCH
Không hiển thị
Xem thêm
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Công ty TNHH Zuellig Pharma Việt Nam
Lầu 5, tòa nhà Maritime Bank, 180 -192 Nguyễn Công Trứ, Q.1, TP. HCM
zuelligpharma.com
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Vị trí Regulatory Affairs Manager do công ty Công ty TNHH Zuellig Pharma Việt Nam tuyển dụng tại , Joboko tự động tổng hợp mức lương Thỏa thuận, tìm thêm việc làm về Regulatory Affairs Manager hoặc công ty Công ty TNHH Zuellig Pharma Việt Nam ở các link phía trên
Giới thiệu công ty
Công ty TNHH Zuellig Pharma Việt Nam
Lầu 5, tòa nhà Maritime Bank, 180 -192 Nguyễn Công Trứ, Q.1, TP. HCM
zuelligpharma.com