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This is Harry from Dynamic Enterprise Solutions. We have urgent requirement with one of our client's, please review below job description and let me know your interest Position ID: DESAL00012150 Title: Systems Administrator Network Location: Waukegan, IL Duration: 12 Months+ Locals Preferred Hiring Manager is looking for self-starting individuals willing to learn new skills and experience is second to self motivated, nice to have experience with Cisco, Teams, Avaya, Five9, or nectar. This position will be in Abbott Park, Illinois- building AP14. Position ID: ABBVJP00010820 Title: Software Quality Assurance Engineer (IEC 62304, 21 CFR 820.30 and EU MDR) Location: North Chicago, IL Duration: 12 Months+ Mush Have medical devices such as IEC 62304, 21 CFR 820.30 and EU MDR. Description: Primarily responsible for representing QA on cross-functional Software as a medical device (SaMD) and Digital Health Software product development teams and executing Quality System requirements to ensure products are developed, tested, and released in compliance with worldwide Medical Device Regulations. Responsible for authoring, reviewing, and approving project documentation associated with the SDLC and design control requirements to support Corporate, Division, FDA, and other regulatory requirements. In addition to these primary areas of focus, quality assurance will also be responsible for creating and maintaining QMS documents for the development of SaMD's and Digital Health Software Products in compliance with global regulations. Responsibilities: . Perform QA activities related to Software as a Medical Device (SaMD) and Digital Health Software Product Development . Ensure compliance with AbbVie's software lifecycle policies and procedures. . Perform design control and risk management activities according to AbbVie's Quality System . Partner with technical teams to ensure design control documentation (Risk Management, Traceability/Linkages) & design change control requirements are met. . Support the creation of regulatory submission documentation. . Identify gaps/improvement opportunities within the Design History File and Risk Management and track to closure. . Initiate assignments independently. Actively lead and participate on development and process improvement teams. Anticipate/resolve quality issues and take preventative actions. . Actively monitor effectiveness of processes and quality of project work, propose and execute quality/process improvements. . Write/review policies/processes/procedures and related documents for the development of SaMD's and Digital Health products in compliance with global regulations. . Apply knowledge of global regulations, guidance's, and Corporate and Function standards. . Lead/assist in the preparation of and support regulatory agency and internal audits. Qualifications: . Bachelor's degree or equivalent is required; preferably in sciences, engineering or other technical/scientific area. . 5+ years of industry experience in Quality Assurance, Development or healthcare related field. Experience in Medical devices, specifically development of Software Medical Devices is desired. . Strong understanding of regulations and standards affecting software medical devices such as IEC 62304, 21 CFR 820.30 and EU MDR. . Experience with creation and maintenance of QMS documents for development of medical devices. . Experience in coordination and planning of complex activities and ability to identify and resolve complex problems through effective use of technical and interpersonal skills. . Product development experience (e.g. approaches for definition of requirements and specification setting for verification and validation). Practical experience in design control and risk management. . Effective use of oral and written communication skills to clearly communicate the quality position, and the actions necessary to resolve issues. . Interpersonal, team, leadership, and negotiation skills to handle conflicting priorities. . Strong oral and written communication skills, excellent interpersonal and cross-cultural skills required. . Capable of clearly presenting and justifying quality requirements to management. Position ID: DYES00011051 Title: SAP Procurement / SAP SRM # of Positions Requested: 1 Duration: 6 months Location/Site: North Chicago, IL ( What Will Make an Impact: . Collaborate with Purchasing, Supplier Relationship, Vendor Management, internal collaborative partners, and other finance and corporate personnel to identify new opportunities and to negotiate project execution as planned. . Assist with coordinating activities across delivery teams and business areas to effectively interact with internal stakeholders during assessment initiatives and ongoing projects. . Maintain knowledge of current procurement trends, vendor capabilities and changes within the procurement landscape for traditional and emerging solutions. Required: . Bachelor's Degree, 10+ years of experience as BSA, 5+ in Procurement . Knowledge of Supplier Management, Indirect Procurement, Information Technology, and general corporate business operations. . Good understanding of supplier onboarding, risk, qualification process and procurement process steps such as bids, RFQs, RFPs, RFIs. . Ability to build strong internal relationships with key stakeholders across multiple business units with strong communication skills. . Ability to be creative and innovative in identifying potential areas that would benefit from procurement initiatives. Preferred: SAP / Ariba knowledge Description Details . Are you open to look at candidates willing to relocate? Open remote but would need to travel to HQ at their own expense as needed . Years of experience/education and/or certifcations required: Bachelor's Degree, 10+ years BSA, 5+ Procurement . What are the top 3-5 skills requirements should this person have? o Supplier Management o Coordination with delivery teams o Exceptional communications Position ID: DESAL00011948 Title: MES Software Developer/ Programmer (Manufacturing Execution Systems (MES) FTPC using Pnuts) Location: Maple Grove, Minnesota Duration: 12 Months+ Locals Preferred Requirements: 5+ years of programming experience in Rockwell's FTPC using Pnuts 3+ years writing design specs and interacting with users to understand requirements . 3+ years proficiency in any object-oriented programming language (preferably Java) and scripting languages like JavaScript . 3+ years of SQL/PL SQL experience (Oracle/SQL Server/MySQL) . Ability to write complex SQL queries to get data from Oracle database Additional qualifications . Knowledge of PLC , SCADA and equipment integration . Knowledgeable in FDA validation requirements preferred including: User Requirement and Design Specs, Business Process Procedures, Design Reviews, Requirements gathering . Experience with the compliance of the systems and batch/unit record and data integrity . Experience with regulatory/compliance documentation and procedures is a plus Thanks & Regard's Harry John Dynamic Enterprise Solutions Inc 1801 Hicks Rd, unit A Rolling Meadows, IL -60008 (847) 719-7902 /C 224-635-0898 Email: [email protected] -- You received this message because you are subscribed to "rtc-linux". Membership options at http://groups.google.com/group/rtc-linux . Please read http://groups.google.com/group/rtc-linux/web/checklist before submitting a driver. --- You received this message because you are subscribed to the Google Groups "rtc-linux" group. 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