{"id":15483,"date":"2025-04-25T05:56:53","date_gmt":"2025-04-25T05:56:53","guid":{"rendered":"https:\/\/peoplelake.asia\/?post_type=awsm_job_openings&#038;p=15483"},"modified":"2025-12-24T16:27:05","modified_gmt":"2025-12-24T16:27:05","slug":"regulatory-affairs-ra-executive","status":"expired","type":"awsm_job_openings","link":"https:\/\/peoplelake.asia\/zh\/?post_type=awsm_job_openings&p=15483","title":{"rendered":"Regulatory Affairs Executive (RA)"},"content":{"rendered":"<p><strong>Job Overview:<\/strong><br>We are seeking a <strong>Regulatory Affairs Executive<\/strong> to support product registration and ensure compliance with medical device regulations in various jurisdictions. The ideal candidate is detail-oriented, organized, and familiar with regulatory documentation and submissions.<\/p>\n\n\n\n<p><strong>Key Responsibilities:<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Assist in maintaining regulatory approvals and product registrations in line with local and international requirements.<\/li>\n\n\n\n<li>Prepare and submit documentation for product registration, license renewals, and endorsements.<\/li>\n\n\n\n<li>Monitor updates in regulatory guidelines and ensure documentation is updated accordingly.<\/li>\n\n\n\n<li>Maintain accurate regulatory records and registration master lists.<\/li>\n\n\n\n<li>Coordinate with regulatory authorities and commercial partners on documentation and endorsements.<\/li>\n\n\n\n<li>Support product vigilance activities including advisory notices, safety actions, and incident reporting.<\/li>\n\n\n\n<li>Distribute and follow up on customer feedback questionnaires; analyse feedback and prepare reports.<\/li>\n\n\n\n<li>Support internal, supplier, and external audits related to regulatory compliance.<\/li>\n\n\n\n<li>Participate in risk management and other cross-functional initiatives as needed.<\/li>\n<\/ul>\n\n\n\n<p><strong>Requirements:<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Diploma or Degree in related field<\/li>\n\n\n\n<li>Basic knowledge of medical device regulatory requirements (e.g., MDA, EU MDR, etc.)<\/li>\n\n\n\n<li>Strong attention to detail and good documentation skills<\/li>\n\n\n\n<li>Good communication and coordination abilities<\/li>\n\n\n\n<li>Ability to work independently and in a team<\/li>\n<\/ul>\n\n\n\n<p>Contact Name: Arthur Lee<\/p>\n\n\n\n<p>Email Address: arthur@peoplelake.asia<\/p>\n\n\n\n<p>Contact Number: 60125805506<\/p>\n\n\n\n<p><\/p>","protected":false},"excerpt":{"rendered":"<p>Job Overview:We are seeking a Regulatory Affairs Executive to support product registration and ensure compliance with medical device regulations in various jurisdictions. The ideal candidate is detail-oriented, organized, and familiar with regulatory documentation and submissions. Key Responsibilities: Requirements: Contact Name: Arthur Lee Email Address: arthur@peoplelake.asia Contact Number: 60125805506<\/p>","protected":false},"author":27,"featured_media":14775,"template":"","meta":{"_joinchat":[]},"class_list":["post-15483","awsm_job_openings","type-awsm_job_openings","status-expired","has-post-thumbnail","hentry","job-category-regulatory","job-type-full-time","job-location-bandar-tasik-selatan","job-industry-manufacturing"],"_links":{"self":[{"href":"https:\/\/peoplelake.asia\/zh\/wp-json\/wp\/v2\/awsm_job_openings\/15483","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/peoplelake.asia\/zh\/wp-json\/wp\/v2\/awsm_job_openings"}],"about":[{"href":"https:\/\/peoplelake.asia\/zh\/wp-json\/wp\/v2\/types\/awsm_job_openings"}],"author":[{"embeddable":true,"href":"https:\/\/peoplelake.asia\/zh\/wp-json\/wp\/v2\/users\/27"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/peoplelake.asia\/zh\/wp-json\/wp\/v2\/media\/14775"}],"wp:attachment":[{"href":"https:\/\/peoplelake.asia\/zh\/wp-json\/wp\/v2\/media?parent=15483"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}