INDUSTRY RESULTS
Description String Industry
Medical Device Technician (MECHANICAL OR ELECTRO-MECHANICAL OR CHEMICAL OR CHEMICALS OR ELECTRICAL) AND (R&D OR "RESEARCH & DEVELOPMENT" OR "R AND D" OR GMP OR MANUFACTURING) AND ("MEDICAL DEVICE" OR "MEDICAL DEVICES" OR "MEDICAL DEVICE ASSEMBLER" OR "MEDICAL DEVICE ASSEMBLY" OR ASSEMBLER OR "MEDICAL DEVICE TECHNICIAN") Medical Device
Product Surveillance Tech (Customer OR CSR OR "Contact Center" OR “Administrative Assistant”) AND (Health OR Clinic OR Med OR Medic OR Medical) AND (FDA OR CDRH OR PMA OR IDE OR MDR CFR OR FOI) Medical Device
Clinical Application Specialist Clinical Application Specialist AND medical device AND territory -intitle: (she OR her) profiles -inurl:dir/ site:www.linkedin.com/in/ OR site:www.linkedin.com/pub/ Medical Device
Tool Maker (DESIGN OR BLUEPRINT OR DRAW OR CREATE) AND (MOULDING OR ASSEMBLING OR MOULD OR GRIND OR ASSEMBLE OR SHAPING OR CUTTING OR DRILL OR MILL) AND CAD AND TROUBLESHOOT AND (TOOL OR “TOOL MAKING” OR TOOLS OR "TOOL MAKER") AND (MACHINE OR MECHANIST OR PROCESS OR DEVICE) AND QUALITY Medical Device
Electro-mechanical Assembler (BUILD OR ASSEMBLER OR ASSEMBLY OR ASSEMBLE OR STRUCTURE OR PRODUCE OR MODIFY OR WELDER OR WELDING OR MECHANIC OR SCREW OR NUT OR DESIGN OR PRODUCTION OR LINE OR OPERATOR OR MACHINE) AND (ASSEMBLE OR ASSEMBLER OR ASSEMBLY) AND (ELECT OR MAGNET OR ELECTROMAGNET OR ELECTROMAGNETIC OR SOLDERING) AND MACHINE Medical Device
• Understand, maintain, and contribute to the improvement efforts with document management processes for the BD Interventional Surgery; includes ensuring proper document templates are used, documents undergo appropriate review and approvals, documents are published with high quality standards; documents are appropriate circulated, and acknowledgements are accurately retained and well organized. • Serve as subject matter expert for document management solution. Support efforts for implementation, training, troubleshooting, user-requests, and transition as needed. • Prepare and maintain documents that support company and QA initiatives, such as process documents, policy documents, SOPs, templates, forms, tracking spreadsheets, meeting minutes, etc. • Maintain quality document systems (e.g., EDMS, LMS, EPR etc.). • Understand, maintain, and contribute to the improvement efforts with record management processes for the organization; includes ensuring record retention conventions and list are maintained and communicated, archiving room protocols are followed, and QA files are organized and maintained. • Support QMS/QA related processes as directed. These activities are likely to include the following: Audits, CAPAs, improvement initiatives, Document Control, Record Control, Safety, QMS/Compliance Awareness and Training, Management Review, etc. • Support customer audit/visit efforts as directed. • Recommend quality improvements and suggestions. • Must be able to work with different departments and individuals and help establish reasonable processes and programs to ensure compliance with all industry regulations and standards. • Other duties and tasks that may be assigned on an as-needed basis. • Strong interpersonal, communication and customer service skills. • Excellent technical writing, grammar and speaking skills; ability to create and edit written material in a clear, concise, and accurate manner. • Strong data analysis, problem analysis, and problem-solving skills. • Ability to encourage progress, promote concepts, and maintain confidentiality. • Strong attention to detail and appreciation for organization/order. • Experience planning, organizing and implementing solutions that are sustainable. • Willingness to actively collaborate, work independently, adapt to changes and changing priorities, and work under deadlines without sacrificing accuracy. • Good time management, prioritization, judgment, and decision-making skills. • Expert level knowledge of EDMS and LMS Systems. • Experience with and/or quality systems / quality control compliance / ISO 13485 activities and or facilitating adult learning sessions, preferred. • Industry specific experience preferred. • Knowledge of tools, concepts and methodologies of QA preferred. • Certifications that may include: Document Management Certified Professional, American Society of Quality (ASQ) Certified Quality Improvement Associate, Quality Auditor, or Six Sigma Green Belt, or similar. (Quality or QA or QMS) And (Document or Documentation or DMS) AND (Control or Maintenance or Development) AND ( EDMS or LMS or EPR ) And ( Record or Report or MBR ) AND( MS-Office or Excel or Word or Outlook) And( SOP)AND( CAPA ) AND(ISO 13485)AND((Lean or sigma or KAIZEN or Kanban or 5s or Green belt ) AND( Medical Devices ) Medical Device
Candidates with Project Management who can support with IT Products and Programs Engaging with Business partners Experience with Salesforce technologies , running programs from start to finish Prefers Hybrid Agile experience compared to Agile methodologies. Role is going to be Mid-Level (2-5) years of experience. Senior programmer or senior level is not required Candidate can work in any time zone Big plus to have a healthcare industry but not requirement Scrum Master with PMS certification would be a nice to have but not required Candidate will be working on JIRA based products Top Skills Client is looking for someone who has Hybrid-agile exp IT Project Manager JIRA Experience with Salesforce technologies Mid-level IT Project Manager with 5 Yrs exp (HYBRID-AGILE OR "HYBRID AGILE") AND (JIRA), IN (CA-US, TX-US, MN-US) AND IN {US}, WITH BACHELOR DEGREE AND [ WORK AUTHORIZATION IS GC,US CITIZEN ] , TITLES= ("PROJECT MANAGER") Medical Device