Responsibilities & Qualifications We are seeking a Control Validation Security Specialist. REQUIRED QUALIFICATIONS Experience 3 years of experience working with DOD1 8500.2 or NIST SP 800-53, and understand the principles of the Risk Management Framework (RMF). 2
Description: The Process Engineer provides support to the operation Manager/Associate Director Operation/ Engineering in implementing improvements, validation and automation to the plant operations and assist in several functions such as writing standard operating procedures (SOPs), develop process flow, review
Description Position Type: Contractor / Consultant – FTC (6-9 Months with possible extension) Location: Piscataway, NJ (onsite - physical presence required) – OR – Chicago, IL (onsite - physical presence required) Reports To: Sr. Director of
Challenge Yourself and Impact the Future! MacDermid Alpha Electronics Solutions, a business segment of Element Solutions Inc (NYSE: ESI), is renowned worldwide for its commitment to revolutionizing the electronics industry. With a legacy spanning over a
Business Process & Project Analyst For more than 100 years, Xerox has continually redefined the workplace experience. XIT Staffing, a division of Xerox dedicated to staffing solutions, is committed to collaborating closely with our internal clients to
Mid Source Validation Desk Officer/ Counterintelligence Specialist Prescient Edge is seeking a Mid Source Validation Desk Officer/ Counterintelligence Specialist to support a Federal government client. As a Mid Source Validation Desk Officer/ Counterintelligence Specialist, you will: Conduct operational analysis
Candidates must have an active Secret clearance and verify, before applying, that you meet the minimum requirements of the position. Data and Software Infrastructure Architecture Engineer Location: Fort Belvoir, VA Clearance: DoD Secret minimum Focus: Supporting
Description: Process Engineer reports to the Manager of Technical Services and plans, executes and functionally directs Process/Cleaning Validation/Study assignments and projects, which require sound pharmaceutical/engineering skills and independent judgment. Works as a team member, educates internal partners on the
Description: The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on
Job Title: Ground Domain Requirements Writer Job Category: Intelligence Time Type: Full time Minimum Clearance Required to Start: TS/SCI Employee Type: Regular Percentage of Travel Required: Up to 50% Type of Travel: Continental US * *
Job Title: Maritime Domain Requirements Writer Job Category: Intelligence Time Type: Full time Minimum Clearance Required to Start: TS/SCI Employee Type: Regular Percentage of Travel Required: Up to 50% Type of Travel: Continental US * *
Description SUMMARY: The Manager of CMO Operations oversees outsourced production, technical transfers, and routine manufacturing activities across multiple contract manufacturing organizations to ensure reliable supply, regulatory compliance, and high-quality performance. You will coordinate between external partners
Description Summary A Sr. Scientist I will be a key technical resource responsible for independently developing methods, generating reliable and interpreting data, using analytical instrument that include HPLC, UPLC, GC, UV/Vis, dissolution apparatus and particle analyzer.
Description SUMMARY: The Quality Assurance Specialist I is a regular employee in a full-time exempt position at Kashiv BioSciences, LLC, in Piscataway NJ. This employee will be responsible for supporting Kashiv BioSciences Quality Assurance management in
Description SUMMARY: The Quality Assurance Specialist II is a regular employee in a full-time exempt position at Kashiv BioSciences, LLC, in Piscataway NJ. This employee will be responsible for supporting Kashiv BioSciences Quality Assurance management in
Description SUMMARY: The Quality Assurance Specialist II is a regular employee in a full-time exempt position at Kashiv BioSciences, LLC, in Piscataway NJ. This employee will be responsible for supporting Kashiv BioSciences Quality Assurance management in
Description The Facility Engineer is a regular employee in a full-time exempt position at Kashiv BioSciences, LLC, in Piscataway, NJ. This employee will be responsible developing, testing, modifying, and creating solutions to technical problems. Essential Duties
Who are we looking for? The Line of Business Leader (LoB) owns the global vision, strategy, and execution to deliver long-term volume and margin growth of the Flexible Printed Electronics line of business globally. This includes
Job Title: Virtual Systems Engineer Job Category: Engineering Time Type: Full time Minimum Clearance Required to Start: Secret Employee Type: Regular Percentage of Travel Required: Up to 10% Type of Travel: Local * * * The
Leidos is seeking multiple SCA-R Validators to assess programs’ security posture and develop reports and recommendations for improvement. These positions can be based out of any of our three locations - Alexandria, VA, Fort Meade, MD,