TEMPORARY

FULL_TIME

CONTRACTOR

ADAPTED_NOW

YEAR

Please submit your resume via iboyett@sterlingmedcorp.com or please contact Isela Boyett at 513-872-2022. For over 30 years, Sterling Medical has matched qualified health care providers with federal facilities throughout the nation as well as overseas.

<div>Sterling Medical is looking for <strong>full time Sterile Processing Technician t </strong>o provide services at the VA Medical Center in Fresno, CA.</div><div> </div><div><strong>Schedule </strong>: Monday - Friday</div><div> </div><div><strong>Qualification:</strong></div><ul><li>possess at least Five years of recent experience</li><li>Must possess either a HSPA Certification or a CBSPD Certification.</li></ul><div><p dir="ltr">Who We Are</p><p dir="ltr">Sterling Medical Corporation is a leader in health care professional staffing. For over 30 years, Sterling Medical has matched qualified health care providers with federal facilities throughout the nation as well as overseas.</p><p dir="ltr"> </p><p dir="ltr">Interested?</p><p dir="ltr">Please submit your resume via iboyett@sterlingmedcorp.com or please contact Isela Boyett at 513-872-2022</p></div>

Sterling Medical

Sterile Processing Technician- Full time

HSPA (High Speed Packet Access)

Healthcare

Healthcare Providers

monster

PERMANENT

If you like staying busy and working with a great team in a beautiful north Fresno office, our client would like to meet you. Send your resume in MS Word format to Fabrizia@denham.net or call (559) 222.5284 if you have any questions.

Great opportunity for long-term part to full time job with room for advancement at a stable and growing company. If you like staying busy and working with a great team in a beautiful north Fresno office, our client would like to meet you.<br/><br/>Description<br/>-Preparation and submission of mail<br/>-E Filing<br/>-Operation of mailing equipment<br/>-Arrange shipping with UPS, FedEx, couriers<br/>-Updates in computer<br/>-Back up to Receptionist<br/>-Additional general office duties as needed<br/><br/>Requirements <br/>-Must be available to work 8-5 on Mondays, Tuesdays, Wednesdays with additional hours available<br/>-Knowledge of Word processing<br/>-Ability to read English<br/>-Excellent communication and organizational skills<br/>-Criminal Background and Credit checks required<br/><br/>To Apply<br/>Send your resume in MS Word format to Fabrizia@denham.net or call (559) 222.5284 if you have any questions. Please refer to the job order number #110328M in your response. Compensation commensurate with qualifications. Visit www.denham.net to see other job listings. All inquiries will be held in the strictest confidence.<br/>

Denham Resources

Operations Specialist Part to Full Time

Administrative Skills

Background Investigation

Communication Skills

English Language

Organizational Skills

Shipping/Receiving

Team Player

Word Processing

Personal computer skills, Microsoft Project, Windows: word processing, project planning, presentation, e-mail, web browsers & spreadsheet software . Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson procedures and guidelines, the duties and responsibilities for this position are: Lead the CI project by interacting with internal and external stakeholders.

<p>Mechanical Engineering Lead</p><p><b>Work Location (State, City and Zip)</b><br/> California, Irvine, 92618</p><p><b>Base salary range (Min. & Max. to be mentioned)</b><br/> 95k to 100K</p><p><b>Experience Range:</b><br/> A minimum of Technical/Engineering Degree with 6+ years of related experience in Medical Device Product Management domain.</p><div align="center" style="text-align:center"></div><p><b>Must Have Technical/Functional Skills</b></p><ul><li>Must possess knowledge of theoretical and practical fundamentals and experimental engineering techniques. </li><li>Knowledge on Quality Management and its tools & techniques </li><li>Knowledge about FDA, 21CFR211 & 820, ISO 13485, ISO 14971, ISO 17025 and compliance regulations </li><li>Knowledge on Medical Device Regulatory Standards, MDD and MDR </li><li>Knowledge of statistics and Minitab </li><li>Knowledge of SolidWorks / CAD to perform changes and revise drawings </li><li>Have first-hand knowledge/experience in creating process flow map, developing project plan using MS Project Gantt's, organize and manage individual project plan/schedule </li><li>Six Sigma Certified preferred </li><li>Knowledge on Plastic Molding, Supplier Management, Packaging, Labeling, 510k submission, Project Risk Management, Verification and Validation </li><li>Presentation to Senior Management </li><li>Excellent interpersonal / communication skills, organizational / planning and project management skills </li><li>Understanding of Marketing & market research strategies </li><li>Personal computer skills, Microsoft Project, Windows: word processing, project planning, presentation, e-mail, web browsers & spreadsheet software </li></ul><div align="center" style="text-align:center"></div><p><b>Roles & Responsibilities</b></p><p>Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson procedures and guidelines, the duties and responsibilities for this position are:</p><ul><li>Lead the CI project by interacting with internal and external stakeholders. </li><li>CIP calculation starting from getting quotation from supplier. </li><li>Finalize the budget considering feasibility study, capital investment, validation expense, DVT samples, bioburden etc. </li><li>Create project plan using Microsoft Project and PowerPoint. </li><li>Knowledge of product and functionalities </li><li>Design change or alternative supplier type projects to achieve type II savings. </li><li>Different approach to achieve the CIP. </li><li>Perform testing, writing test protocols, test reports, conduct design review meetings. </li><li>Understand all project activities, time estimation and execution plan </li><li>Understand what tests to perform, getting alignment with R&D. </li><li>Knowledge requirements review, process validation </li><li>Finalizing RR form, review and finalize validation documents. </li><li>Execution of change request and supplier change requests. </li><li>Responsible for communicating business related issues or opportunities to next management level </li><li>Responsible for ensuring subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition </li><li>Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures </li><li>May supervise/lead and provide technical guidance to lower-level personnel </li><li>Performs other duties as assigned </li></ul><p/><p/><p>Regards,<br/> Vivekanand </p><p>LinkedIn: <a href="https://www.linkedin.com/in/vivekanand0551/" rel="nofollow" style="color:#0563c1;text-decoration:underline">https://www.linkedin.com/in/vivekanand0551/</a><br/></p><p/>

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