Regulatory Services Manager APAC Pharma

The successful applicant will guide a company through the complex process of getting and keeping products legal and safe for market. They act as the bridge between the organization and health authorities (like the KKM, MOH, FDA etc), managing submissions, tracking regulatory changes, and overseeing product compliance. Providing regulatory support and advice to suppliers, customers, and Brenntag business, in order to be compliant with regulatory requirements, for the Pharma product range and geography assigned.

Main tasks:

• Supporting the Pharma commercial teams on topics including regulatory, legal compliance, quality, and product safety.
• Document preparation, handling product registration applications ensuring drugs are legally authorized for the markets intended.
• Completion of technical and regulatory information requests from customers within the pharmaceutical industry (questionnaires, supply chain agreements, QAA’s & TA’s).
• Contribute as part of a team to maintain the APAC document management system to keep product and supplier information up to date.
• Communicate with authorities, clients, suppliers, and associates.
• Monitor regulatory legislation, environment, changing landscapes, and implications for the organization.
• Develop and implement internal standards, procedures, and work instructions.
• Maintain and administrate regulatory database and provide regulatory education and advice.
• Request product and supplier information directly from manufacturers and indirectly via other internal channels.
• Process Change Control Notifications.
• Creation and ongoing update of product regulatory information in standardized information packs.
• Support of customer, regulatory, and 3rd party risk assessments and audits.
• Reporting and documenting customer requests via KPIs.

Job Requirements

• Qualified Pharmacist holding a current Pharmacy License.
• Experience leading the Regulatory Affairs leading a team.
• Knowledge of Pharma industry requirements and regulations (GxPs, regulatory requirements around supply and end use of raw materials, excipients, and active substances).
• Previous experience working with regulatory documentation for products supplied into the Pharma sector.
• Fluent in English (speaking and written).
• Team player, strong communication and interpersonal skills, with ability to work across all levels and functions.

Brenntag TA Team