Sorry, this job is no longer accepting applications. See below for more jobs that match what you’re looking for!

Sccm Engineer

Expired Job

Robert Half Technology Newbury Park , CA 91320

Posted 3 months ago

My client in Ventura County is seeking a SCCM Engineer for a publishing company. This SCCM Engineer must have 5 years of experience deploying and client management across all SCCM products. For immediate consideration, please send resumes to Ali Scott at

Title: SCCM Engineer

Target Salary: 100k

Benefits: M/D/V ndash; paid parking / 401k w/matching, 100% tuition reimbursement for anyone wanting to complete BS degree

nbsp;

Top Skills:

5 years of experience

SCCM

Deployment and patching

They can work 1 day remote (after probation period)

nbsp;

nbsp;

Job Requirements

Must have experiencd with the following:

5 years of experience

SCCM

Deployment and patching

Windows server

3 years of experience with the following technologies: Citrix XenApp/XenDesktop, Group Policy Objects (GPO), Automation and Scripting language/techniques (PowerShell, VBS, etc), Microsoft Deployment Toolkit (MDT), Windows Desktop/Laptop (Window 7 and 10)

Powershell scripting

nbsp;

For immediate consideration, please send resumes to Ali Scott at

nbsp;

nbsp;

Skills:
Citrix, Laptop, Management, PowerShell, Windows
Permanent


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
lc_ad

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
Process Engineer Drug Substance (Jp4664)

3 Key Consulting

Posted Yesterday

VIEW JOBS 11/18/2018 12:00:00 AM 2019-02-16T00:00 <strong>Job Title:</strong>  Process Engineer – Drug Substance (JP4664)<br /> <strong>Location: </strong>Thousand Oaks, CA<br /> <strong>Employment Type: </strong>Contract<br /> <strong>Duration:</strong> 4+ months<br /> <strong>Business Unit: </strong>Drug Substance Technology & Engineering<br />  <br /> 3Key Consulting Inc. is looking for a <strong>Process Engineer </strong>with 5 - 6 years of production support experience (experience with at scale processes) and biologic manufacturing experience for a global bio-pharmaceutical company.<br />  <br /> <strong>Job Description: </strong><br />   <ul> <li style="padding: 0; margin: 0;">The successful candidate will apply process engineering knowledge in support of technology transfer and clinical and commercial drug substance manufacturing. </li> <li style="padding: 0; margin: 0;">This individual will provide dedicated process engineering support for human therapeutic products (biological drug substance) in clinical development through commercial production. </li> <li style="padding: 0; margin: 0;">Scope includes: transfer processes and process improvements from the laboratory into the manufacturing facility and between manufacturing sites; provide on-the-floor technical support for successful scale-up, transfer of process technology, and for routine clinical and/or commercial production; lead data trending and advanced statistical process analysis</li> <li style="padding: 0; margin: 0;">Provide technical support for all process related deviations (NCs), CAPAs and change controls; </li> <li style="padding: 0; margin: 0;">Provide technical support for new equipment, technology and capital projects in the facility; identify and support process related operational excellence opportunities;</li> <li style="padding: 0; margin: 0;">Manage Process Validation activities occurring at the site; presentation of process performance at team and management meetings</li> <li style="padding: 0; margin: 0;">Process modeling to guide process development activities, identify process implementation issues and drive optimization</li> <li style="padding: 0; margin: 0;">Technical project management; support of regulatory filings and inspections.  </li> </ul>  <br /> <strong>Basic Qualifications:</strong><br /> Doctorate degree and 0-2 year of directly related experience <br /> OR <br /> Master’s degree 6+ years of directly related experience <br /> OR <br /> Bachelor’s degree and 8+ years of directly related experience <br /> <br /> <strong>Preferred Qualifications</strong>:  <br />   <ul> <li style="padding: 0; margin: 0;">MS in Chemical/Biochemical Engineer or other biological engineering discipline and 8 years Process Engineering experience related to biochemical engineering and/or protein biochemistry, scale-up principles and manufacturing of biologics (cGMP) </li> <li style="padding: 0; margin: 0;">Upstream and/or Downstream process knowledge and hands on cell culture and/or purification pilot/clinical/commercial experience with regard to the manufacture of a biological drug substance. </li> <li style="padding: 0; margin: 0;">In-depth understanding of chromatography, ultrafiltration, normal flow filtration, virus inactivation and virus filtration operations <br /> AND/OR </li> <li style="padding: 0; margin: 0;">In-depth understanding of cell culture process scale up, mass oxygen transfer, metabolism profiling, process deviation impact to growth and quality attributes, harvest/clarification processes, raw material including media component impact to cell culture. </li> <li style="padding: 0; margin: 0;">Good knowledge of aseptic processing/techniques. </li> <li style="padding: 0; margin: 0;">Process validation, process characterization and process monitoring experience </li> <li style="padding: 0; margin: 0;">Experience in supporting regulatory inspections </li> <li style="padding: 0; margin: 0;">Process development experience in supporting cGMP manufacturing at large scale </li> <li style="padding: 0; margin: 0;">Good written and verbal communication skills </li> <li style="padding: 0; margin: 0;">Experience in preparing regulatory filings and participation in regulatory inspections </li> <li style="padding: 0; margin: 0;">Process development and optimization experience with late stage or commercial products </li> <li style="padding: 0; margin: 0;">Process equipment design and evaluation expertise </li> <li style="padding: 0; margin: 0;">Experience with risk analysis methodologies </li> <li style="padding: 0; margin: 0;">Independently motivated with ability to multi-task and work in teams </li> <li style="padding: 0; margin: 0;">Excellent organizational, leadership, teamwork, and communication skills are required as well as the ability to work effectively in a dynamic and challenging environment with enthusiasm and a proactive positive attitude. </li> </ul> <br /> <br /> <br /> <strong>Employee Value Proposition:</strong><br /> Opportunity to provide manufacturing support to cutting edge technology at Amgen.<br /> <br /> <strong>Interview Process:</strong><br /> Phone interview first and then In-person interview. <br /> <br /> We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at the other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.<br />   3 Key Consulting Thousand Oaks CA

Sccm Engineer

Expired Job

Robert Half Technology