Regulatory Affairs Associate (Cebu)

Industry Category	Healthcare	Position	Pharmacy
Recruitment Department		Number Of Recruits	several
Work Location	Cebu Cebu City	Nature Of Work	Full Time
Gender Requirements	Male	Marriage Requirement	No marital status restrictions
Education Level	College Diploma	Work Experience	No work experience restrictions
Age Requirement	Above 18 years old	Salary Package	Negotiable
Updated Date	2022-10-20	Valid Until	Long-term validity

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 over 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 Distribution, Clinical Reach, Sales & Marketing, Patient Centered Services, and Community Pharmacies. Zuellig Pharma is the leading provider of distribution services to manufacturers in the life science industry in the Asia Pacific region. With operations in 13 countries or territories Zuellig Pharma has strong market positions, critical mass, broad geographic coverage and significant potential for continuing growth.

Purpose of the Position:

We are looking for a Regulatory Affairs Associate - Registered Pharmacist.

The Regulatory Affairs Associate is responsible for the compliance of regulatory, statutory and quality standards by ensuring that business transactions, such as order processing, picking, quality checking, material deliveries and transfers, including pull-out of Regulated Drugs, are aligned to the government legal requirements and quality standards of the company. She is primarily responsible in the annual renewal of FDA License to Operate and PDEA License to Handle Dangerous Drugs of the Branch.

The RA Associate will also act as a Site document Controller, who is responsible of the control of documents and records, in compliance with the ZP Regional Standards and ISO 9001 current version, aligned to the company’s vision, mission and directions to ensure achievement of customer fulfillment and service objectives of the company.

Requirements:

Registered PharmacistIn-depth knowledge of International Standards (Good Clinical Practices, ISO, etc)With Project Management skills/experienceSAP experience preferredCommunity and Hospital Pharmacy experience.Warehouse and Logistics experience preferred.Willing to be assigned in Cebu Mandaue City, Cebu