Quality Sys Spec

The successful incumbent will be responsible for quality compliance and quality assurance activities for our Hong Kong office. How You’ll Make an Impact: Quality Compliance Activities Support the setup, maintenance and ongoing management of distributor and importer quality systems in accordance with the Code of Practice for Listed Distributors and Importers of Medical Devices for the Hong Kong Service Center. Ensure the implementation of appropriate control measures for ordering, supply and distribution of medical devices to authorized customers and distributors. Attain and maintain necessary licenses and permits including: Antibiotic Permit Wholesale Dealer Licence(s) for Poisons Wholesale Licence(s) for Dangerous Goods Part 1 and Psychotropic Drugs, as applicable Import Licence(s)/Certificate(s) for Dangerous Goods Part 1 and Psychotropic Drugs, as applicable Work closely with regulatory bodies during audits and inspections, resolving issues and implementing changes to ensure compliance and smooth operations. Support the setup and implementation of Hong Kong Good Distribution Practice (HK GDP) standards. Conduct routine checks for updates in relevant legislations and ordinances, such as CAP 134 Dangerous Drugs Ordinance, CAP 138 Pharmacy and Poisons Ordinance and CAP 137 Antibiotics. Review and update Standard Operating Procedures (SOPs) and Work Instructions (WIs) to reflect any newly controlled substances or regulatory changes. Manage and control drug fulfilment processes, including physical handling, record‑keeping and ensuring data integrity of drug records in Hong Kong. Apply critical thinking and problem‑solving skills to identify root causes of issues and implement corrective actions effectively. Support in any relevant activities, as assigned. Quality Assurance Activities Support activities related to nonconformance, corrective actions and effectiveness checks. Collaborate with service center personnel to continuously improve quality procedures and methods. Perform activities related to quality assurance functions, including document inquiry, retrieval of archived records, management of electronic records, and SAP transactions related to Quality Notifications. Conduct audits and oversight of third‑party wholesale distributors and importers, supporting internal and external audit processes. Draft, revise or obsolete controlled documents used at the service center. Essential Job Responsibilities Apply and maintain the relevant licenses in Hong Kong. Find the gap between regulations and the current quality management system, work out solutions and implement. Oversee and audit the 3rd‑party vendors to ensure the wholesaling and import licensing activities are covered. Setup and maintenance of the distributor and importer Quality system requirements at the Hong Kong service centre. Be responsible for operational related CAPA plan and perform activities related to nonconformance, corrective actions and effectiveness checks. Be responsible for establishment, maintenance and optimisation of the local SOPs. Perform or support internal and external audit of the quality management system for the service centre. Organise and conduct quality related training to employees and distributors. Prepare, maintain and update library or external regulatory standards, reference and guidance documents. What You Bring Minimum bachelor’s degree in pharmacy (Hong Kong) or internal auditor qualification preferred. At least 3 years’ work experience in Quality Assurance and holding wholesale and/or import licence for handling pharmaceuticals or medical device IVD. Experience in ISO9001, ISO13485 &/or GDP. Hong Kong Registered Pharmacist is preferred. Other knowledge, skills, abilities Good planning/organising skills/attention to details. Proactive approach to resolving issues. Good analytical, communication, problem solving, critical thinking, and computer skills. Good working knowledge of regulatory requirements. Working knowledge of policies, practices and procedures relating to Quality Assurance. Good oral and written English and Cantonese/Mandarin. Who We Are: For 70 years, Bio‑Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing and marketing a broad range of high‑quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Recently voted a Best Place to Work, Bio‑Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. Benefits: Bio‑Rad’s biggest asset is our people, and this is the reason why our Total Rewards deliver programmes that provide value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Our offerings serve to enrich the overall health, wealth and well‑being of our employees and their families through the various stages of an employee’s work and life cycle. We’re proud to offer comprehensive medical plans and insurance, wellness programmes, extensive learning and development opportunities and more. EEO Statement: Bio‑Rad is an Equal Employment Opportunity/affirmative action employer, and we welcome candidates of all backgrounds. Veterans, people with disabilities, and people of all races, ethnicities, genders, ages and orientations are encouraged to apply. Agency Non‑Solicitation: Bio‑Rad does not accept agency resumes, unless the agency has been authorised by a Bio‑Rad Recruiting Representative. Please do not submit resumes unless authorised to do so. Bio‑Rad will not pay for any fees related to unsolicited resumes. #J-18808-Ljbffr