社名
社名非公開
職種
品質マネージャー, ディレクター, ヘッド
業務内容
...
Lead and grow a team, build cutting-edge quality systems, and develop your expertise in a dynamic global biopharmaceutical company.■About the companyOur client is a leading global biopharmaceutical company dedicated to developing innovative treatments for rare diseases. They foster a collaborative and supportive work environment with a strong commitment to both employee growth and patient care. Their Japan-based team is crucial to their global success.■Role & ResponsibilitiesYou will be a key leader in ensuring the highest standards of regulatory compliance and quality across multiple disciplines within the organization. You'll lead a team of quality professionals, collaborating closely with global counterparts to implement and improve quality assurance systems. You will drive change management initiatives and play a critical role in ensuring compliance with global and local GxP guidelines. This is a fantastic opportunity to develop your leadership and technical expertise within a leading global biopharma company.■Main tasks include- Lead the development and implementation of quality assurance systems and procedures.- Manage and mentor a team of quality professionals.- Collaborate with global teams on regulatory compliance and quality initiatives.- Drive change management processes and ensure adherence to GxP guidelines.- Develop and maintain quality agreements with contract manufacturing organizations (CMOs).- Manage and optimize the quality budget.If you are interested in this exciting opportunity, apply now.We look forward to hearing from you.#LI-Hybrid#LI-KN
求められる経験
■Requirements
- Minimum of 5 years of experience in GQP/GMP in the pharmaceutical industry.
- Experience in drafting and negotiating Quality Agreements (QAGs) with CMOs.
- Proven experience in leading and mentoring teams.
- Strong understanding of Japanese and global pharmaceutical regulations.
- Expert knowledge of GQP/GMP principles and practices.
- Excellent communication and collaboration skills in both Japanese and English.
- Bachelor's degree in pharmacy or a related scientific field.
- Experience with biological products is highly preferred.
- Ability to work effectively in a dynamic and fast-paced environment.
- Strong leadership and decision-making skills.
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1,200 ~ 1,600万円
賞与
-
雇用期間
期間の定めなし
show more
社名
社名非公開
職種
品質マネージャー, ディレクター, ヘッド
業務内容
Lead and grow a team, build cutting-edge quality systems, and develop your expertise in a dynamic global biopharmaceutical company.■About the companyOur client is a leading global biopharmaceutical company dedicated to developing innovative treatments for rare diseases. They foster a collaborative and supportive work environment with a strong commitment to both employee growth and patient care. Their Japan-based team is crucial to their global success.■Role & ResponsibilitiesYou will be a key leader in ensuring the highest standards of regulatory compliance and quality across multiple disciplines within the organization. You'll lead a team of quality professionals, collaborating closely with global counterparts to implement and improve quality assurance systems. You will drive change management initiatives and play a critical role in ensuring compliance with global and local GxP guidelines. This is a fantastic opportunity to develop your leadership and technical expertise within a leading global biopharma company.■Main tasks include- Lead the development and implementation of quality assurance systems and procedures.- Manage and mentor a team of quality professionals.- Collaborate with global teams on regulatory compliance and quality initiatives.- Drive change management processes and ensure adherence to GxP guidelines.- Develop and maintain quality agreements with contract manufacturing organizations (CMOs).- Manage and optimize the quality budget.If you are interested in this exciting opportunity, apply now.We look forward to hearing from you.#LI-Hybrid#LI-KN
...
求められる経験
■Requirements
- Minimum of 5 years of experience in GQP/GMP in the pharmaceutical industry.
- Experience in drafting and negotiating Quality Agreements (QAGs) with CMOs.
- Proven experience in leading and mentoring teams.
- Strong understanding of Japanese and global pharmaceutical regulations.
- Expert knowledge of GQP/GMP principles and practices.
- Excellent communication and collaboration skills in both Japanese and English.
- Bachelor's degree in pharmacy or a related scientific field.
- Experience with biological products is highly preferred.
- Ability to work effectively in a dynamic and fast-paced environment.
- Strong leadership and decision-making skills.
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1,200 ~ 1,600万円
賞与
-
雇用期間
期間の定めなし
show more