Job Description

Job Overview:
ARK Diagnostics, Inc. seeking a highly skilled and detail-oriented  Regulatory Affairs Specialist II to join our team. In this role, you will be responsible responsible for supporting US/EU/UK/ROW device listing/registration, regulatory assessment of product or process changes, regulatory submission of marketing applications and activities related to new and on-market products meant to ensure compliance with local and international regulatory requirements.

The Regulatory Affairs Specialist II plays a supportive role by partnering across business functions to identify data and prepare documentation needed for regulatory clearance, product registration and license maintenance of products worldwide.

The ideal candidate for this role will have a degree in a life sciences field such as biology, chemistry, or biomedical engineering and at least 2 years of experience in regulatory affairs in the medical device industry. You will also have excellent communication skills and the ability to work effectively in a collaborative team environment. If you are looking for an exciting opportunity, we encourage you to apply!

Principal Duties and Responsibilities:

• Responsible for international regulatory-related request(s) including but not limited to product registration, licensing, permits and/or renewal(s).
• Coordinate the market expansion activities with ARK business partners/distributors in various geographies.
• Support the preparation of Regulatory documents for new product market clearance, compile content for International Regulatory submissions to sustain product lifecycle including, but not limited to, 510(k),  De Novo , and IVDR technical documentation files for CE-marking, Pre- and Post-Market Notifications, CLIA Categorizations, Supplements, Change Notifications, and country-specific product registrations.
• Support the timely dissemination of international regulatory requests and/or information to applicable authorized representatives, distributors, customers, as deemed appropriate.
• Support senior staff with post-market safety and surveillance activities, product recalls, corrections, if applicable.
• Ensure appropriate maintenance of policies, procedures, processes, and practices to comply with US and international regulations regulatory requirements, under the guidance of senior staff.
• Responsible for the upkeep and maintenance of all regulatory affairs documentation/files for guidance and reference.
• Assist with the review of product labeling, promotional, and advertising materials.
• Support internal and external quality and regulatory audits.
• Provide senior staff support for training activities for cross-functional teams on various regulatory topics and processes.
• Support cross-functional product development teams and other projects, as necessary.

Requirements

• BS/MS in the Life Sciences, Biomedical Engineering, Regulatory Affairs, or equivalent discipline.
• At least 2 years of relevant experience in domestic and international Regulatory Affairs Medical Device industry, preferably with  In-Vitro Diagnostics (IVD); Assays is a plus.
• Sound knowledge of U.S. and European/International Regulatory requirements and Quality System Standards, as applied to Medical Devices (especially IVDs) => 21 CFR § 820, ISO 13485, ISO 14971, MDSAP, IVDD and IVDR (EU) 2017/746
• Experience with international product registrations, license renewals and /or permits.
• Experience working directly with notified bodies, authorized representatives and/or international regulatory authorities.
• Experience with FDA Regulatory submission pathways, such as 510(k), desirable
• Regulatory Affairs Certification (RAC), desirable
• Attention to Quality at every stage of the product life cycle.
• Excellent organization and prioritization skills.
• Effective communication skills, both written and oral.
• Ability to think critically, assess risks, produce creative solutions.

Benefits

ARK Diagnostics, Inc. anticipates that the annual base salary for the  Regulatory Affairs Specialist II  position could range between $95,000-$115,000. Compensation will depend, in part, on the successful candidate’s credentials for the role, including education, qualifications, and type as well as length of experience. Any offered salary is also based on internal equity, internal position salary ranges, and market data. Annual base salary is just one piece of the total rewards program offered by ARK. Eligible roles come with a comprehensive benefits package and may also qualify for a variable annual bonus, contingent on company and/or individual performance in accordance with company policy.

Benefits

• 401(k) and 401(k) matching
• Health, dental, and vision insurance
• Health Savings Account (HSA) and Flexible Spending Account (FSA)
• Life insurance
• Paid time off
• Employee Assistance Program (EAP)
• Tuition reimbursement
• Referral program

Onsite Work Requirements

This position is fully onsite at our Fremont, CA facility.

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