Regulatory Affairs Manager

Katalyst Healthcares & Life Sciences • Seattle, WA

175d

About The Position

Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices. We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Requirements

• Bachelor's degree required.
• 5 years direct experience in Regulatory Affairs in a Medical Device Company required.
• Strong interpersonal and communication skills.
• Proficient in Microsoft Office.
• Advanced written communication skills.

Responsibilities

• Support and advise cross-functional teams and communicate APAC regulatory requirements and challenges effectively to meet project needs and company objectives.
• Oversee and direct the development of priorities, timelines, receipt of technical information from appropriate sources, and the preparation of regulatory documentation for new products, amendments of approved products, and submissions that support the maintenance of existing licenses.
• Support in implementation of policies, procedures, practices, and strategies to facilitate support of in-country product registrations in APAC.
• Work closely with regional APAC regulatory team to develop and drive process efficiencies for APAC regulatory submissions.
• Review and evaluate issues that may create regulatory or business obstacles and propose solutions.
• Monitor APAC regulations/guidelines and the impact of changing/evolving regulations on submissions, practices, and procedures, and communicate to appropriate stakeholders.
• Manage the performance and career development of direct reports.

What This Job Offers

• Career Level: Entry Level
• Education Level: Bachelor's degree