Medical Assembler/Medical Lab Operator

Tekwissen Saint Paul , MN 55101

Posted 6 months ago


Client: St Jude Medical

Medical Lab Oper
Location: Minnetonka, MN Plymouth, MN
Duration: Contract to hire

Note : Microscope Knowledge / Experience is required in Medical field

Job Description :

  • Labeling, Packaging And Inserting Data Sheets For Pharmaceuticals.
  • Packaging/Labeling, Weighed Material Before Sending Out To Patient Dispensaries
  • Organized and ran various types of secondary pharmaceutical packaging orders
  • Perform daily packaging room cleaning and document on cleaning logs
  • Experience in using a microscope
  • Working in a clean room manufacturing environment assemble medical devices
  • Operate within standard operating procedures (SOPs) and assembly drawings
  • Clean and maintain work area
  • Properly turn off and lock out equipment when not in use
  • Measure and record process parameters and report results to supervision
  • Adhere to production schedules and report material shortages

Company Description

TekWissen provides a unique portfolio of innovative capabilities that seamlessly combines clients insights, strategy, design, software engineering and systems integration. Our tightly integrated offerings are tailored to each client's requirements and span the services spectrum from Application Development/Maintenance, testing, IT Consulting & Staffing for IT Infrastructure Management through strategic consulting and industry oriented Business Process. Our end-to-end Business Process as a Service (BPaaS) solutions support complex, high-value, knowledge-based work. Combining applications, platforms, infrastructure, knowledge processes, and domain expertise allows us to deliver greater efficiency and innovative business capabilities. You should have positive, constructive attitude and the ability to work both independently and in a team environment.
See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Download the
LiveCareer app and find
your dream job anywhere

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Manager Medical Affairs


Posted 6 days ago

VIEW JOBS 9/14/2018 12:00:00 AM 2018-12-13T00:00 This position will serve as the clinical expert with primary focus on the respiratory care product lines interacting with marketing, regulatory, and research & development to ensure clinical activities are aligned with business objectives. Objective is to create strong clinical evidence to drive market adoption and provide guidance on medical risks and outcomes during product development. The Manager Medical Affairs is responsible for developing clinical protocols, conducting clinical activities to collect outcomes evidence, support new product development approvals and reimbursement, and drive publication plans to disseminate clinical outcomes data. This position will be the expert within the therapeutic category and develop strong relationships with thought leaders and key investigators to drive the clinical agenda. ESSENTIAL DUTIES AND RESPONSIBILITIES * Develop clinical plans and protocols for new and existing products through strong cross-organizational collaboration & understanding of business needs. * Design clinical projects to collect outcomes data supporting market adoption, new product approvals, and reimbursement. This includes various forms of research such as review articles, health outcomes data, post-marketing studies, and clinical trials. * Develop clinical project plans including key milestones, budget needs, and resource deployment (i.e. internal sources, clinical research organizations (CRO), and institution on site staff). * Conduct clinical studies including with responsibility for the following: * Identification of appropriate sites/investigators. * Qualifying, enrolling and training investigators and investigator's site personnel in study protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements. Conduct product training & set up with intended users prior to clinical study * Monitoring study progress, preparing study documents and providing updates on study status. * Identifies, establishes, and maintains collaborative relationships with key investigators and institutions strategic to the appropriate use of company products for the purposes of business and research collaboration * Establish relationships with key thought leaders and investigators to seek guidance & validation of clinical plan and study protocols. * Leads and facilitates advisory boards and key thought leader activities * Establish and manage publication plans to ensure high impact dissemination of clinical content. * Interacts with Regulatory Authorities to answer follow-up questions, provide investigation details. * Provides guidance on medical risks and outcomes during product development. * Travel to key thought leaders, clinical trial sites, and key scientific meetings/tradeshows (20%). * Perform other duties and projects as assigned. * 3-5 years experience and knowledge of clinical research programs including methodologies, processes, and timelines. * Experience in the planning, conducting, and managing studies in a clinical program from study start-up to regulatory submission. * Strong project planning, leadership, negotiation and presentation skills as well as an ability to contribute creative yet practical solutions to problems. * Strong cross-organizational collaboration with internal teams and external investigators or project partners. * Strong organizational skills with ability to multi-task and manage multiple projects in parallel. * Demonstrated interpersonal skills to successfully partner with individuals to build relationships with business contacts, customers, and regulatory entities Hill-Rom Saint Paul MN

Medical Assembler/Medical Lab Operator