Regulatory Affairs Pharmacist

SUNFU SOLUTIONS, INC.; Philippines; On-site; PHP 240,000 - 480,000; Full time

Job summary

SUNFU SOLUTIONS, INC. is looking for a licensed Pharmacist to join its regulatory affairs team. The role focuses on registering medical devices, supplies and medicines with regulatory bodies and ensuring timely compliance with all required permits and papers.

Fresh graduates are welcome to apply and on-site work is required. The ideal candidate will monitor regulatory developments, coordinate with suppliers, and support other teams on regulatory matters to help strengthen product compliance and

Qualifications

• Must be a licensed Pharmacist in the Philippines.
• Experience with registering medical devices, supplies or drugs is a plus.
• Regulatory affairs exposure is preferred but not required.
• Willing to work on-site.
• Entry level/fresh graduates are welcome to apply.

Responsibilities

• Register medical devices, supplies and medicines within required timelines.
• Secure permits and papers related to company products.
• Identify issues and provide solutions for regulatory concerns.
• Meet deadlines to obtain necessary documents from suppliers.
• Provide updates on FDA/DOH regulatory news applicable to healthcare.
• Assist other teams with regulatory and product needs.
• Perform administrative tasks as part of the admin team.

Skills

Regulatory awareness

Documentation skills

Attention to detail

Education

Pharmacist license Philippines

Job description

Join us to make an impact in public health in our country! We serve and give solutions to the healthcare sector and we are devoted to bringing quality medical machines to improve lives and strengthen local healthcare capacity building.

Qualifications:

• Candidate must be a licensed Pharmacist

• Work experience having registered medical devices and supplies or drugs is a plus.

• Prior experience in regulatory affairs or product registration is preferred but not required.

• Must be willing to work on-site.

• Entry level/fresh graduate candidates are welcome to apply.

Duties and Responsibilities:

• Goal is to successfully register all medical devices, supplies and medicines needed by the company in the required timelines.

• Able to secure other needed permits and needed papers related to products of the company.

• Able to identify issues and provide solutions with regulatory concerns.

• Must be deadline-driven in getting the needed documents from suppliers.

• Gives timely updates on news from FDA or DOH that is applicable in the healthcare industry.

• Assist other teams in the company in relation to regulatory needs and product needs.

• Perform administrative tasks as part of the administrative team that provides administrative support to the company.