Regulatory Services Manager APAC Pharma

The successful applicant will guides 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 authorised for the markets intended.

Completion of technical and regulatory information requests from customers within the pharmaceutical industry (questionnaires supply chain agreements QAAs & TAs).

Contribute as part of team to maintain 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 organisation.

Develop and implement internal standards procedures and work instructions.

Maintain and administrate regulatory data base 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