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, QAA’s & TA’s). · 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 Brenntag TA Team Brenntag is the leading global distributor of chemicals and ingredients, committed to connecting customers and suppliers within networks. We add value for our customers and partners every step of the way: through our product knowledge, innovation, and sustainable solutions, combined with our passion for service excellence and commitment to safety. Headquartered in Essen, Germany, and with more than 17,500 experts at about 600 locations in 72 countries, our two global divisions, Brenntag Essentials and Brenntag Specialties, offer a full range of industrial and specialty chemicals and ingredients. Therefore, our clients and partners can count on us for global reach combined with local agility and execution. As an employer, we embrace diversity and foster a sense of community and collaboration in an environment where employees are encouraged to share ideas and work together. We engage our employees in the company’s mission for collective success, by building long-term stability and safety through trust and clarity across the organization. We believe in empowering our employees to reach their full potential and shape the future. For more information, please visit www.brenntag.com

Regulatory Services Manager APAC Pharma.

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