รายละเอียดงานResponsibilities:
•Manage all activities related to Regulatory Affairs (pre-submission, submission, and life cycle maintenance) of the medical devices and other products as assigned by RA head.
•Review, analyze and co-ordinate data for variations submission to marketed products according to priorities and responses to questions and/or comments from FDA authorities.
•Monitor progress of variations approval process with the regulatory authority. Liaise and negotiate with the relevant authorities to facilitate and secure expeditious regulatory approvals.
•Review all current approved packaging materials to ensure the contents are in accordance with local regulatory requirements, local regulatory approved documents, and reference document. Development of the packaging material artworks those are aligned with the local regulatory approval and other related forms/activities as requested by the supplier in order to support the related functions in a timely manner.
•Ensure compliance of regulatory requirements, company & principles policies. Keep up to date for law & regulations knowledge related to regulatory works.
•Update and maintain regulatory databases.
•Provide Hospital Bidding & Enlisting document to marketing as requested
•Consult, review, and advise on promotional materials to published under marketing and sales activities such as advertising, leaflets, sales promotion programs and all activities related to Regulatory Affairs
•Facilitate communication between cross functional stakeholders to make the company meet the targets.
•Cooperate with all related functions and concerned parties for PV and medical information management of medical devices and other products as assigned by RA head.
Interested applicants are invited to send application with updated resume indicating qualifications and experience, expected salary by email: jidapab@biogenetech.co.th