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2nd shift
Job Title: Tool Maker III
Scope of position:
Plan, design and fabricate fixtures, complex tooling and general machining to assist and support various production departments by planning layout work and sequence of operations utilizing hand tools, precision measuring tools and perform set-ups on machine shop equipment and precision metal cutting equipment.
Hours of work/work schedule: 2nd shift, 8 hours from 2:30pm to 11pm (Monday through Friday)
PPE required - safety glasses and steel toed shoes (provided by client).
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1st shift Monday - Friday
OT occasionally needed
Travel not required
PPE will be needed - company will reimburse costs
Hard skills that are needed:
• Perform building related tasks such as woodworking, framing, drywall, painting, etc.
• Perform tasks such as welding of various materials, electrical, plumbing and HVAC
• Ability to troubleshoot, diagnose and repair equipment as necessary
• Possession of personal hand tools
Scope of Position: Troubleshoot and repair all support equipment and facility related items.
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The assignment may be extended to end of April based on the individual performance.
Perform Operational Risk Control Self Assessments including process flow development, risk/control identification and documentation, and working with internal partners. - Support administration of control testing plan as required by the FMA BURCO Division Risk Managers. - Coordinate follow-ups, communicate status, and reporting as required. - May perform additional duties as backfill for existing staff during the CCAR surge period.
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- The Compliance Technology Organization is seeking an implementation engineer to support the migration of legacy sanction platforms to CGI Hotscan.
- Install and configure vendor software. Work with internal teams such a s DBAs, middleware, Websphere and unix admins to facilitate installations and troubleshooting.
- Provide production support on existing platform Ace Pelican.
- Strong Technical skills required to support OFAC related applications running on Unix platforms (ie: Java/J2ee Web technologies, Shell Scripts, SQL, Oracle, Websphere. MQSeries, Tidal).
- Debug and trouble shoot defects during QA & UAT in accordance, supplying recommendations and evaluations. Support testing and implementation of solutions.
- Analyze, design and create specs and documentation for features and/or system back end processes
- Prepare specs/detailed design documents and perform coding / resolution assignments for the team.
- Document procedures and operational “runbooks” for applications supported.
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Attorney, Senior Paralegal and/or Contract Negotiations experience will be considered:
Reporting to the head of the Contracting and Negotiations Group ("CNG"), these contractor positions should be filled by attorneys/paralegals/contract negotiators with strong backgrounds in reviewing and understanding third-party vendor contracts as well as legal and regulatory terms. Specifically, the contractor position will interface, as needed, with Business Units, Strategic Sourcing and Bank Subject Matter Experts (“SMEs”) (e.g., Legal, Tax, EIC, etc.) to negotiate, on behalf of SME stakeholders, legal and regulatory terms of third-party vendor contracts and also provide internal advice and guidance related to such contracts. Familiarity with technology transactions, software licenses, strategic sourcing and general procurement within the banking and financial services industry is ideal.
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- Requirements Elicitation, Gathering, Clarification, and Analysis. Participate in the creation of Business Requirements Document.
- Use Case Analysis and Documentation.
- Data Analysis and Documentation and proficiency in SQL.
- Create Functional Design Document.
- Create Detailed Design Document.
- Ensure business requirements are organized and coherent for application architects and developers to understand.
- Test Planning and Coordination.
- Ensure application meets business requirements.
- Create and Track Test Plans, Cases, and Scripts.
- Migration Planning and Coordination. Provide Project Support (Issues Tracking, User Training).
- Create Application Documentation (User Guide, Operations Guide, Training Manual, etc.).
- Familiarity with modern web application designs and concepts.
- Strong knowledge of Software Development Life Cycle (SDLC).
- Work with business for requirements. Work with technical team to write the detailed and functional design documents.
- Individual will have 3-5 years of experience.
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- Rsponsible for the design, modeling, development and testing of a machine, structure or system. Develops functional requirements.
- Understands and applies standard engineering principles.
- Creates prototypes to evaluate preliminary designs and test how a machine, structure or system operates.
- Designs and tests components, and integrates components to produce final product.
- Monitors quality of products and controls the efficiency of processes.
- Evaluates a design's overall effectiveness, reliability, and safety.
- Investigates root causes of failures to maintain quality and recommend improvements.
- The work with focus on R&D for stent programs. This is a great way to get exposure to high complexity programs
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Review, assess and process complaints. Creation and submission of US Medical Device Report (MDR) and EU Vigilance Reports to external regulatory agencies. You will also support the response to any queries received from regulatory agencies in relation to complaint events or post market regulatory reports. Detail oriented and excel skills required.
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This position reports into a PMO embedded within R&D. In this position, the project manager will manage a range of program and project types. One project will require completion of development, launch, and closure activities to launch new high-value kit products in two different geographies. Other projects may include portfolio-wide design changes to Neurovascular products and organizing/tracking sustaining engineering activities in special areas (coordinating internal staff and external consultation). Another assignment will assess the effectivity of a recent improvement program to capture Lessons Learned, and then formulate another round of improvements (working with planning, distribution, distribution centers, and supplier quality functions to refine business processes to augment Value Added Services at two distribution centers). As needed, assignments may include leading emergent work-streams for EU-MDR.
Manages multiple projects and orchestrates the results to achieve a broad program goal. Plans and implements schedules and monitors program from inception through delivery. Defines and reports program roadmap, status, development issues and success metrics. Identifies and monitors areas of risk. Continuously seeks opportunities to improve cost, performance and schedule. Builds and manages to budgets. Facilitates communication and coordination among projects. Manages stakeholder engagement and satisfaction. Maintains awareness of trends, business conditions and internal process and practices impacting component projects or overall program.
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This Technical Publication Specialist will be a resource who contributes to new product development and design change activities in the areas of label design, technical writing, development of artwork/images and development/improvement of processes for improved efficiency and compliance. The resource will work as a team member as well as lead teams on special activities having business impact.
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- Responsible for supporting the implementation of Regulatory Affairs and Quality Assurance systems and procedures relating to Domestic and/or International regulatory requirements.
- Provides administrative support to a department or individual.
- Knowledge of applicable international regulations and standards (QSR, MDD, ISO 13485, CMDCAS, etc.) and willingness to train others in quality assurance/GMP-related topics.
- Develop and maintain positive relationships with regulatory agencies through professional oral and written communications.
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- Reesponsible for supporting the implementation of Regulatory Affairs and Quality Assurance systems and procedures relating to Domestic and/or International regulatory requirements.
- Provides administrative support to a department or individual.
- Knowledge of applicable international regulations and standards (QSR, MDD, ISO 13485, CMDCAS, etc.) and willingness to train others in quality assurance/GMP-related topics.
- Develop and maintain positive relationships with regulatory agencies through professional oral and written communications.
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Senior Manufacturing Engineer - Leading Medical Device Company
Job Summary
This position independently leads complex activities and tasks in support of manufacturing requirements.
- Activities and tasks are conducted on materials, products, processes, and equipment.
- Receives minimal direction /review and is viewed as an expert in one or more in-house technologies.
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Alibaba Pictures Group Limited (“Alibaba Pictures”) is the flagship unit of Alibaba Group’s entertainment arm and its core businesses includes four segments: film and television production centered on IP (intellectual property); internet-based promotion and distribution combining internet technologies and traditional off-line distribution; the building and operation of e-commerce platforms for entertainment as an extension of the Alibaba Group ecosystem and international operations that consolidate global resources, technologies and talents in order to participate in the global entertainment industry. Alibaba Group is the largest shareholder of Alibaba Pictures, its mission is to make it easy to do business anywhere. The company is the largest online and mobile commerce company in the world in terms of gross merchandise volume. The company provides the fundamental technology infrastructure and marketing reach to help businesses leverage the power of the Internet to establish an online presence and conduct commerce with hundreds of millions of consumers and other businesses. Alibaba Pictures is well positioned to leverage and integrate its Alibaba Group’s resources and technology to carry on the mission of developing its cultural businesses. Focusing on innovation in the cultural industry, Alibaba Pictures bases its operations on the principle, “customer first” and its business development on the powers of the Internet and big data. Alibaba Pictures is a public company listed on the Hong Kong Stock Exchange (HKSE: 1060) and the Singapore Exchange (SGX:S91).
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Summary /Overview:
Receive daily task, install copper and fiber to the desk top ports, trouble shoot outages.
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Receive daily task, install copper and fiber to the desk top ports, trouble shoot outages.
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