Manager / Sr. Manager, Regulatory Affairs

Shifamed; Doha; On-site; QAR 291,226 - 436,839; Full time

Job summary

Shifamed is seeking a Manager / Sr. Manager in Regulatory Affairs to lead the regulatory strategy and submissions for its medical devices. This role involves close collaboration with Clinical, Quality, and R&D teams to support U.S. regulatory activities and global clinical studies.

The ideal candidate should have over 10 years of experience in the industry, particularly with FDA submissions, and be familiar with international regulatory pathways. This position offers a unique opportunity to shape regulatory strategy for a clinical-stage company.

Qualifications

• 10+ years of Regulatory Affairs experience within the medical device industry.
• Experience supporting clinical-stage medical device programs.
• Strong understanding of clinical evidence requirements.

Responsibilities

• Develop and execute global regulatory strategies.
• Lead preparation and submission of U.S. regulatory filings.
• Support clinical studies including regulatory submissions across multiple countries.

Skills

FDA medical device submissions

Regulatory strategy development

Cross-functional leadership

Clinical study support

Excellent written and verbal communication

Education

Bachelor's degree in Engineering, Life Sciences, or related field

Job description

Position: Manager / Sr. Manager, Regulatory Affairs

Location: Doha, Qatar

Job Id: 666

# of Openings: 1

Akura Medical Overview

Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana™ Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing NavIQ™, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&D and manufacturing center in Doha, Qatar.

ABOUT SHIFAMED

Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.

Description

This Manager / Sr. Manager, Regulatory Affairs will serve as a key member of the cross-functional team, partnering closely with Clinical, Quality, R&D, and Executive Leadership to support U.S. regulatory activities and lead global clinical studies and international market expansion. The ideal candidate brings strong FDA medical device experience combined with hands‑on knowledge of international regulatory pathways, agency interactions, and clinical study support across Europe, the Middle East, and other global markets. This is a unique opportunity to help shape regulatory strategy for a clinical-stage medical device company as it expands global clinical activities, and prepares for international commercialization.

Responsibilities, Skills & Hands-On Experience

Regulatory Strategy & Product Development

• Develop and execute global regulatory strategies for Akura Medical's thrombectomy and catheter-based cardiovascular technologies.
• Serve as regulatory lead on cross-functional product development teams from concept through commercialization.
• Provide regulatory guidance on design controls, risk management, verification and validation activities, labeling, and product changes.
• Partner with Quality and R&D teams to ensure compliance with FDA, MDR, ISO 13485, and applicable international requirements.

FDA Regulatory Affairs

• Lead preparation, review, and submission of U.S. regulatory filings, including IDE's, 510(k)'s, supplements, and other regulatory submissions as applicable.
• Monitor evolving FDA requirements and assess impact on development and commercialization plans.

International Regulatory Expansion

• Develop regulatory strategies and market access plans for Europe, the Middle East, and other international markets.
• Support CE Mark and MDR-related activities in partnership with Notified Bodies and external regulatory consultants.
• Lead country-specific registration activities and regulatory submissions across key international markets including Qatar, UAE, Saudi Arabia, and other MENA countries.
• Establish and maintain relationships with regulatory authorities, notified bodies, and international regulatory partners.

Clinical & Regulatory Operations

• Partner closely with Clinical Affairs to support global clinical studies, including IDE, PMCF, registries, and post-market studies.
• Provide regulatory guidance on protocol development, clinical study design, and regulatory approval pathways.
• Support regulatory submissions associated with clinical trial approvals across multiple countries and regions.
• Participate in investigator meetings, regulatory inspections, audits, and agency interactions.

Agency Interactions & Compliance

• Represent the company during interactions with FDA, Notified Bodies, Ministries of Health, and other regulatory authorities.
• Support preparation for regulatory inspections and audits.
• Maintain awareness of evolving global regulatory requirements and communicate potential impacts to leadership.
• Contribute to regulatory intelligence activities and long-term market expansion planning.

Cross-Functional Leadership

• Collaborate with Clinical, Quality, Manufacturing, Supply Chain, and R&D teams to ensure regulatory requirements are incorporated throughout the product lifecycle.
• Provide regulatory leadership for change assessments, design modifications, and lifecycle management activities.
• Support Executive Leadership with regulatory risk assessments, timelines, and strategic planning.

Qualifications & Experience

• Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, or related field.
• 10+ years of Regulatory Affairs experience within the medical device industry; cardiovascular, endovascular, or interventional products strongly preferred.
• Direct experience with FDA medical device submissions, including IDE's, PMA's, 510(k)'s, or PMA supplements.
• Experience supporting clinical-stage medical device programs and global clinical studies.
• Working knowledge of EU MDR, ISO 13485, ISO 14971, IEC 62304, and international regulatory frameworks.
• Experience interacting directly with regulatory agencies, notified bodies, and international health authorities.
• Familiarity with MENA regulatory pathways (Saudi SFDA, UAE MOHAP/DOH, Qatar MOPH, etc.) is highly desirable.
• Strong understanding of design controls, risk management, clinical evidence requirements, and regulatory strategy development.
• Excellent written, verbal, and presentation skills.
• Ability to thrive in a fast-paced, entrepreneurial environment and work effectively across global teams.

Preferred Qualifications

• Experience with thrombectomy, vascular intervention, pulmonary embolism, structural heart, or electrophysiology technologies.
• Prior experience supporting regulatory expansion into Europe, the Middle East, and emerging international markets.
• Experience participating in FDA meetings, regulatory inspections, and Notified Body audits.

Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.

NOTICE TO CANDIDATES

Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to [e-mail].