Head of Quality - Third Party Operations, Pharmaceutical Industry

Singapore  |  Permanent

Published 01/03/2012

• Leadership role
• Regional position

About Our Client
Our client is one of the world's leading generics manufacturers with extensive operations across the globe. They are experiencing tremendous growth within the region.

Job Description

Reporting to the Head of TPO you will manage all quality aspects at Third Party Contract Manufacturers for the region and ensure compliance with cGMP, regulatory requirements, the Quality Manual are conducted according to the relevant SOPs. You will ensure compliance with the Quality manual, the effective Quality Agreement, cGMP and regulatory requirements according to local SOPs. You will represent QA at technical meetings with Third Parties and establish good working relationships with clear relationships with clear communication. You will ensure that a valid QA agreement is in place which clearly defines cGMP-relevant activities at the Third Party as well as product details.

The Successful Applicant

• You are a graduate in Biochemistry, Chemistry, Pharmacy, Microbiology or other related sciences.
• You have a minimum 10 years experience in the Pharmaceutical Industry as well as in production.
• You have significant experience in compliance.
• You have previous or current experience of working in a matrix structure within a multinational.
• You are a strong communication, performance orientated and willing to travel on a regular basis.

What's On Offer
This is an exciting opportunity to join an industry leading organisation in a senior regional appointment.

Apply for this job
Apply online using the form below or phone Andrew Davis on + 65 6643 9700 quoting jobref H1146500

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