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Regulatory Affairs Associate (Cebu)

2022-10-20 08:31IP Location 菲律宾2920
Area:Cebu Cebu City
Industry Category:Healthcare
Position:Pharmacy
Department:
Number Of Recruits:several
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:Above 18 years old
Salary Package:Negotiable

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
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