Regulatory Affairs Specialist II - #26-25769
Fremont, CAContract / Temporary$33/hrSeen 1 day agoSeen in employer's feed 1 day ago
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Job overview
The Regulatory Affairs Specialist II supports international registration of IVD products by preparing and maintaining regulatory documentation and submission materials. The role coordinates information gathering, prepares technical files for CE marking, and works with international counterparts to obtain product approvals and renewals. Submissions must be accurate, well supported, and compliant with applicable statutes, regulations, guidelines, and company procedures.
Skills & qualifications
Skills
Qualifications
Full job description
$33 per hour
Fremont, CA
Contract
Duration: 12 months
Position Summary
- The Regulatory Affairs Specialist II will draft, assemble, and file original documentation and submission materials for new or existing products to regulatory authorities to assure that all submissions are accurate, of high quality and well supported by literature and regulatory foundations, are presented in a manner to facilitate review, and are in conformance with appropriate statutes, regulations, and guidelines
Key Responsibilities:
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The Regulatory Affairs Specialist II will join existing team and provide support for International Registration of IVD products.
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Tasks will include
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Initiation, collection, and coordination of information of regulatory documents for various purposes.
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Preparation and maintenance of product technical files for CE marking
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Organization and preparation of documents for international submissions, including drafting reports, and preparing documentation for submissions
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Coordination with international counterparts to obtain product approvals and renewals.
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Maintaining logs and trackers.
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Organize, update, and maintain regulatory documentation in accordance with department and company procedures.
Minimum Requirements:
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Bachelors degree in a scientific, engineering or related field is required
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2+ years of experience working in regulatory environment –RA/QA/R&D/QC
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Working knowledge and experience with IVD products
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Knowledgeable in the aspects of regulatory strategy creation, design control, cGMP/Quality Systems, IVDR and import/export requirements
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Strong oral and written communication skills
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com .
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.
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