Job opening - Regulatory Affairs Senior Manager in 東京23区 | Randstad

summary

東京23区, 東京都
¥8,000,000 - ¥12,000,000 per year, 年収800 ～ 1,200万円
permanent

job category
biotechnology & pharmaceutical

job details

社名
社名非公開

職種
薬事、メディカルライティング

業務内容 ...

Lead regulatory strategies and submissions for innovative oncology products in a dynamic and collaborative environment.■About the companyOur client is a leading precision oncology company focused on conquering cancer globally through its proprietary blood tests, vast data sets, and advanced analytics. They leverage technology, clinical development, and regulatory expertise to drive commercial adoption and improve patient outcomes. The company fosters a collaborative and innovative work environment.■Role & ResponsibilitiesYou will be responsible for developing and implementing regulatory strategies for innovative oncology products in the Japanese market. You will lead cross-functional teams, manage submissions to the PMDA, and ensure compliance with all relevant regulations. This role offers the opportunity to significantly impact the lives of cancer patients and contribute to the growth of a leading precision oncology company.■Main tasks include・Lead the development and execution of regulatory strategies for new and existing products.・Manage the preparation and submission of regulatory documents to the PMDA.・Collaborate with cross-functional teams to ensure alignment on regulatory requirements.・Monitor and interpret changes in regulatory landscape.・Lead communication with PMDA/MHLW to ensure timely approvals.・Identify and mitigate regulatory risks.If you are interested in this exciting opportunity, apply now.We look forward to hearing from you.#LI-Hybrid

求められる経験
■Requirements
・Bachelor's degree or higher in life sciences, engineering, or a related field.
・8+ years of experience in regulatory affairs, with at least 3 years in IVD, genetic testing, precision medicine, or oncology.
・Proven experience in managing regulatory submissions to the PMDA.
・Strong understanding of Japanese regulatory requirements for medical devices and IVDs.
・Excellent communication skills in Japanese and English.
・Strong organizational and project management skills.
・Experience leading and mentoring teams.
・Experience with QMS and design control.
・Familiarity with genomic/molecular technologies.
・Experience negotiating with regulatory authorities.

保険
健康保険　厚生年金保険　雇用保険

休日休暇
土曜日　日曜日　祝日

給与
年収800 ～ 1,200万円

賞与
Included. Plus RSU
雇用期間
期間の定めなし

show more

社名
社名非公開

職種
薬事、メディカルライティング

業務内容
Lead regulatory strategies and submissions for innovative oncology products in a dynamic and collaborative environment.■About the companyOur client is a leading precision oncology company focused on conquering cancer globally through its proprietary blood tests, vast data sets, and advanced analytics. They leverage technology, clinical development, and regulatory expertise to drive commercial adoption and improve patient outcomes. The company fosters a collaborative and innovative work environment.■Role & ResponsibilitiesYou will be responsible for developing and implementing regulatory strategies for innovative oncology products in the Japanese market. You will lead cross-functional teams, manage submissions to the PMDA, and ensure compliance with all relevant regulations. This role offers the opportunity to significantly impact the lives of cancer patients and contribute to the growth of a leading precision oncology company.■Main tasks include・Lead the development and execution of regulatory strategies for new and existing products.・Manage the preparation and submission of regulatory documents to the PMDA.・Collaborate with cross-functional teams to ensure alignment on regulatory requirements.・Monitor and interpret changes in regulatory landscape.・Lead communication with PMDA/MHLW to ensure timely approvals.・Identify and mitigate regulatory risks.If you are interested in this exciting opportunity, apply now.We look forward to hearing from you.#LI-Hybrid ...

求められる経験
■Requirements
・Bachelor's degree or higher in life sciences, engineering, or a related field.
・8+ years of experience in regulatory affairs, with at least 3 years in IVD, genetic testing, precision medicine, or oncology.
・Proven experience in managing regulatory submissions to the PMDA.
・Strong understanding of Japanese regulatory requirements for medical devices and IVDs.
・Excellent communication skills in Japanese and English.
・Strong organizational and project management skills.
・Experience leading and mentoring teams.
・Experience with QMS and design control.
・Familiarity with genomic/molecular technologies.
・Experience negotiating with regulatory authorities.

保険
健康保険　厚生年金保険　雇用保険

休日休暇
土曜日　日曜日　祝日

給与
年収800 ～ 1,200万円

賞与
Included. Plus RSU
雇用期間
期間の定めなし

show more

experience
■Requirements ・Bachelor's degree or higher in life sciences, engineering, or a related field. ・8+ ye

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