
51 - 200 employees
💊 Pharmaceuticals
Consulting • Healthcare • Pharmaceuticals
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.
🕒 April 29
🗣️🇯🇵 Japanese Required
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51 - 200 employees
💊 Pharmaceuticals
Consulting • Healthcare • Pharmaceuticals
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.
• 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.
• 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.
• Flexible work arrangements
Apply Now🕒 April 9
1 - 10
Compliance Engineer working on maintaining compliance certifications for regulated industries in the APAC region including Finance, Telecom, and Government sectors.
🕒 March 25
11 - 50
💊 Pharmaceuticals
⚕️ Healthcare Insurance
🎯 Recruiter
Regulatory Affairs Specialist managing artwork development within a global regulatory solutions company based in Japan. Collaborating with cross-functional teams to ensure compliant artwork production.
🕒 March 25
11 - 50
💊 Pharmaceuticals
⚕️ Healthcare Insurance
🎯 Recruiter
Regulatory Affairs Specialist ensuring compliant artwork development for pharmaceutical and biotech firms. Collaborating with cross-functional teams and managing documentation in a remote environment.
🕒 March 12
Clinical Consultant leading regulatory strategy for Japan in a fully remote capacity. Collaborating on clinical trials and regulatory submissions for life sciences organizations.
🗣️🇯🇵 Japanese Required
🕒 February 10
1001 - 5000
Specialist in Compliance for Santen, a global company with a focus on eye health, ensuring compliance with laws and ethical standards.
🗣️🇯🇵 Japanese Required