THE FORCE CT GmbH
51 - 200 employees
📦 Logistics
🏭 Manufacturing
💼 Consulting
Logistics • Manufacturing • Consulting
THE FORCE CT GmbH is an implementation consultancy firm offering comprehensive consulting and hands-on implementation services specifically for pharmaceutical, medical device, and healthcare organizations. The company focuses on facilitating business transformation, quality regulatory affairs, pharmacovigilance, toxicology, medical device launch and distribution, and supply chain management. It emphasizes a collaborative and flexible approach, encouraging creativity, initiative, and continuous personal and organizational growth. THE FORCE fosters a culture of trust, responsibility, and diversity, committed to delivering high-quality solutions to clients.
Senior Regulatory Affairs Manager
Job not on LinkedIn
🕒 April 29
🗣️🇯🇵 Japanese Required
Where this job comes from
Posted on THE FORCE CT GmbH's careers page, not through a job board
First seen by Remote Rocketship April 29
THE FORCE CT GmbH
51 - 200 employees
📦 Logistics
🏭 Manufacturing
💼 Consulting
Logistics • Manufacturing • Consulting
THE FORCE CT GmbH is an implementation consultancy firm offering comprehensive consulting and hands-on implementation services specifically for pharmaceutical, medical device, and healthcare organizations. The company focuses on facilitating business transformation, quality regulatory affairs, pharmacovigilance, toxicology, medical device launch and distribution, and supply chain management. It emphasizes a collaborative and flexible approach, encouraging creativity, initiative, and continuous personal and organizational growth. THE FORCE fosters a culture of trust, responsibility, and diversity, committed to delivering high-quality solutions to clients.
📋 Description
• Navigate challenges in regulatory strategy and life-cycle measures. • Handle complex regulatory topics with ease. • Communicate with health authorities (i.e. PMDA) and clients or partners. • Knowledgeable in regulatory procedures and guidelines in Japan for medicinal products and beyond. • Explore new product types.
🎯 Requirements
• You have an academic degree in pharmacy or a related scientific field. • At least 10 years of experience in Regulatory Affairs in an international environment. • Experience in clinical or regulatory strategy. • Strong communication skills. • Excellent team worker and thrive in a multi-national environment. • An eye for detail.
🏖️ Benefits
• Flexible work arrangements
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