Jobs in Japan, Shibuya
Teva Associate Director Clinical Operations Japan, Shibuya
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- Lead the development of the local operational plans for clinical deliverables for assigned programs, effectively implementing design excellence in line with the Clinical Development Plan (CDP) and Global operational project management plan
- Participate in global departmental core activity processes and tasks, such as regular global operation team meeting
- Ensure alignment of operational plans and activities with the overall Clinical Development Team strategy while maintaining effective communication, including identification of risks and points of escalation
- May participate in due diligence activities by providing operational input as appropriate
- Collaborate with CQA to establish local audit plan to ensure timely resolution of CQA audit findings and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable)
- Oversee management of Japan local CROs, local vendors and consultants, working closely with Procurement/ Lead CPM for performance and quality metrics
- Ensure effective collaboration between global and local CROs by liaising with vendors and Teva functions
- Assist with site activations as necessary and review translated essential documents
- Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan
- Ensure the appropriate information is communicated to management including but not limited to KPIs, achievements, risks, and mitigation plans
- Ensure compliance with Quality standards (SOPs, GCP, etc.)
- Plan and manage local Investigators’ and Kick-off meetings in close collaboration with the Global teams, including the study vendors
- Ensure that all local essential documents are present and that the TMF is complete
- Develop in-depth knowledge in relevant indications and clinical trials methodology and applies the relevant information in recommending changes to better satisfy business requirements
- Assist local CRO-CRA to Support Site Engagement for clinical studies in Japan
- Evaluate clinical operation strategies to meet requirements for approval of products in Japan
- Prepare scientific or medical documentation to support clinical studies or regulatory procedures
- May support Japan Reference Listed Drug (RLD)/comparator sourcing, purchasing and shipping
- Support regulatory affairs teams in dossier preparation, especially CSR and its appendix
- Evaluate, develop, manage and optimize vendor portfolio in Japan
- BA degree (preferred Graduate/MSc degree) in applicable discipline (medical/pharmaceutical sciences)
- Strong management and supervisory experience in a global company. Can be experienced in managing and developing a group of people for a minimum of 2 years
- Extensive knowledge of GCPs, ICH guidelines, clinical operations and Japan regulations
- Strong experience in vendor and CRO management
- Experience in process improvement and design as well as project management and budget expertise
- Experience as an operations person in obtaining JNDA approval for one or more NCE products
- Experience in receiving and managing PMDA GCP inspections
- Good Information Technologies orientation
- Good English language knowledge
- At least 8 years previous experience in innovative medicine pharmaceutical industry or 8 years over all combined experience in a Contract Research Organization and innovative pharmaceutical industry, sound knowledge of the clinical landscape in Japan
- Travel Requirements: Ability to travel with overnight stays, as necessary, up to 30%
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
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Honeywell Field Service Engr Japan, Shibuya
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Support the development of on-site installation, servicing and repair processes of complex equipment and systems. You will provide technical presentations to an audience of customers, other industry peers and competitors. You will support revision and correction of work instructions and customer-facing training guides used by field installation specialists. You will drive continuous improvement initiatives in the processes related to field services and product development. You will support cross-functional groups to quickly fix any administrative difficulties relating to delivery and installation of proper equipment. You will act as an escalation point for Field Service Specialists, Service Engineers, and other stakeholders.
Key Responsibilities- Validate customer request
- Educate customer and field technicians
- Write documentation used by field technicians
- Ensure Right and Fast Delivery
- Previous industry experience
- Previous technical/installation experience
- Previous customer service experience
- Good written and oral communication
- Advanced Degree
- Good presentation skills
- JOB ID: req477889
- Category: Customer Experience
- Location: Japan
- Nonexempt
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Honeywell Project Engr Japan, Shibuya
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Be part of a team assessing and driving achievement of program specific performance within Honeywell [SBG]. You will partner with world class engineers and leaders to develop program cost, schedules and milestones, define technology roadmaps, and drive improvements in engineering quality and productivity.
Key Responsibilities- Schedule and Milestone development_x000D_
- customer relationships
- Understand technology
- Cost development
- Budget analysis
- Bachelor’s degree from an accredited institution in a technical discipline such as the sciences, technology, engineering or mathematics
- Follow specific action plans
- Promote customer relationships
- Understand technology
- Being a creative person
- You artfully convey even subtle or complex messages clearly, as appropriate for the topic and audience.
- You find the correct balance between demand and capacity when establishing priorities for the organization.
- People who consistently take the initiative to get things done
- People who are Self-motivated and able to work with little supervision
- Some experience in engineering
- JOB ID: req477890
- Category: Engineering
- Location: Japan
- Exempt
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Honeywell General Manager Regional LOB IA Leader Japan, Shibuya
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CRITICAL BEHAVIORS
• Embrace Transformation, Innovate and Create Value forCustomers and Win Together
• Drive Accountability culture - Leads with passion, highenergy and urgency.
• Be Courageous - will push the organization, peers anddirect reports & is comfortable being unpopular
• Ability to deal with ambiguity and complexity across aglobal, matrixed organization. Creates order, prioritization and clarity ofpurpose. Knows how to balance long-term and short-term thinking
Qualifications/ Experience/ Knowledge
• 15+ years experience in a team leadership role including experience of managing a high performing team with proven track record of growth and profit/margin expansion
• Needs to be comfortable communicating in English
• Graduate/ undergraduate engineering degree with an MBA or other advanced degree is preferred.
• Proven experience in working closely with a peer group comprising of cross function leaders in Customer Marketing, Finance, Customer Service, Technical Service, Supply chain and logistics experience; with ability to cohesively work together with an integrative approach to meet goals.
• Should have ability to understand financial data and identify appropriate actions indicated by variances to ensure key metrics are achieved.
• Demonstrated ability to develop a long term Strategic business plan; demonstrated capability to execute in line with plan, influence or directly manage resources and investment across multiple functions.
• Strong business acumen, leadership, and strategic program execution skills, process driven with strong analytical mindset.
Additional Information
- JOB ID: req475596
- Category: General Management
- Location: Japan
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Honeywell Physics Intern Japan, Shibuya
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Implementing sample environments in support of laboratory experimentation
Performing low temperature laboratory experiments
Supporting the design and development of integrated solutions with cryogenics being a key component
Partnering with the Principal Investigator, Program Manager, and the Project Engineer for project execution
MINIMUM QUALIFICATIONS:
- Currently pursuing Bachelor’s degree (or higher) from an accredited college or university in Physics, Material Science or Engineering
- Must graduate May 2024 or later
- Must continue enrollment degree program upon completion of internship
- Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. citizen, U.S. permanent resident, or have asylum or refugee status in the U.S.
WE VALUE:
- Experience with Microsoft Office products, including Excel, Word, Project, PowerPoint, and Outlook
- Excellent analytical skills
- Good communication skills and the ability to work effectively with other organizations and individuals at all levels
- Current security clearance for work on government contracts
- Proven track record of working with systems investigating physical phenomena, particularly as applied to cryogenic systems
- Demonstrated ability to design, analyze, operate, build, and test complex systems
Additional Information
- JOB ID: req456673
- Category: Engineering
- Location: 303 S. Technology Ct.,Broomfield,Colorado,80021,United States
- Nonexempt
- Due to US export control laws, must be a US citizen, permanent resident or have protected status.
These jobs might be a good fit
- Lead the development of the local operational plans for clinical deliverables for assigned programs, effectively implementing design excellence in line with the Clinical Development Plan (CDP) and Global operational project management plan
- Participate in global departmental core activity processes and tasks, such as regular global operation team meeting
- Ensure alignment of operational plans and activities with the overall Clinical Development Team strategy while maintaining effective communication, including identification of risks and points of escalation
- May participate in due diligence activities by providing operational input as appropriate
- Collaborate with CQA to establish local audit plan to ensure timely resolution of CQA audit findings and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable)
- Oversee management of Japan local CROs, local vendors and consultants, working closely with Procurement/ Lead CPM for performance and quality metrics
- Ensure effective collaboration between global and local CROs by liaising with vendors and Teva functions
- Assist with site activations as necessary and review translated essential documents
- Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan
- Ensure the appropriate information is communicated to management including but not limited to KPIs, achievements, risks, and mitigation plans
- Ensure compliance with Quality standards (SOPs, GCP, etc.)
- Plan and manage local Investigators’ and Kick-off meetings in close collaboration with the Global teams, including the study vendors
- Ensure that all local essential documents are present and that the TMF is complete
- Develop in-depth knowledge in relevant indications and clinical trials methodology and applies the relevant information in recommending changes to better satisfy business requirements
- Assist local CRO-CRA to Support Site Engagement for clinical studies in Japan
- Evaluate clinical operation strategies to meet requirements for approval of products in Japan
- Prepare scientific or medical documentation to support clinical studies or regulatory procedures
- May support Japan Reference Listed Drug (RLD)/comparator sourcing, purchasing and shipping
- Support regulatory affairs teams in dossier preparation, especially CSR and its appendix
- Evaluate, develop, manage and optimize vendor portfolio in Japan
- BA degree (preferred Graduate/MSc degree) in applicable discipline (medical/pharmaceutical sciences)
- Strong management and supervisory experience in a global company. Can be experienced in managing and developing a group of people for a minimum of 2 years
- Extensive knowledge of GCPs, ICH guidelines, clinical operations and Japan regulations
- Strong experience in vendor and CRO management
- Experience in process improvement and design as well as project management and budget expertise
- Experience as an operations person in obtaining JNDA approval for one or more NCE products
- Experience in receiving and managing PMDA GCP inspections
- Good Information Technologies orientation
- Good English language knowledge
- At least 8 years previous experience in innovative medicine pharmaceutical industry or 8 years over all combined experience in a Contract Research Organization and innovative pharmaceutical industry, sound knowledge of the clinical landscape in Japan
- Travel Requirements: Ability to travel with overnight stays, as necessary, up to 30%
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
These jobs might be a good fit
