$25 - 35 hourly
Number of Applicants
:000+
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Job Posting Summary: Seeking a Regulatory Affairs Specialist to manage updates and compliance for technical files and labeling under the new IVDR requirements, ensuring seamless transition from IVD Directive.
Job Requirements:
Bachelor's degree in biochemistry, biology, medical technology, or related fields.
3-5 years of experience in Regulatory Affairs (RA), Quality Assurance (QA), Research and Development (R&D), Manufacturing, or Project Management within the In Vitro Diagnostic (IVD) industry.
Familiarity with CE Marking and IVDR Technical Files.
Experience with change requests for product labeling.
Preferred Skills:
Knowledge of FDA and CE marking requirements for IVD products.
Job Responsibilities:
Support the transition of Bio-Rad products from IVD Directive requirements to the new In Vitro Diagnostic Regulation (IVDR).
Update labeling to comply with IVDR requirements and revise technical files as necessary.
Work cross-functionally to ensure labeling conversion aligns with planned timelines.
Monitor manufacturing schedules, track change requests, and ensure accuracy in labeling tracking logs.
Update previous revisions of IVDR Technical Files to the latest template with all necessary attachments.
Track RA Regional notifications and follow-ups, and monitor product restrictions as required.
Pay: 25-35
Benefit offerings include medical, dental, vision, term life insurance, short-term disability insurance, additional voluntary benefits, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State or local law; and Holiday pay upon meeting eligibility criteria. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs which are direct hire to a client.
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