Keymark-FloridaLakeland
Keymark Corporation of Florida, an aluminum extrusion manufacturing plant, is actively interviewing applicants for. Bachelor of Science degree in Electrical, Industrial, or Computer Engineering is desired. ...
NCH Healthcare SystemNaples
The Project Manager, EPMO Activation and Tracking, is responsible for overseeing assigned projects, ensuring projects (1) meet agreed upon timelines, (2) follow EPMO guidelines, policies, and procedures, and (3) operate within project scope and budget.
The Project Manager will drive assigned project...
Katalyst Healthcares & Life SciencesWorcester
Responsibilities:
Cleaning Validation Expertise: The primary responsibility of the Cleaning Validation Specialist is to develop, execute, and oversee cleaning validation protocols for pharmaceutical and biotech facilities.
Hands-On Experience...
Artech LLCWarren Grove
Job Description: Validation Specialist
Warren, NJ--Onsite
Work Schedule: Mon - Fri, Business Hours
6 months contract
The Validation Specialist, Computerized Systems, is responsible for performing initial and routine validation activities for GxP...
Artech LLCSummit (NJ)
Job Description: Minimum 50% onsite required every week(Candidate is supposed to align the onsite days with manager and be available onsite when manager requests)
6 months Contract
The Specialist works cross-functionally to execute validation...
Pyramid Consulting, IncSummit (NJ)
Immediate need for a talented Manufacturing Systems Validation Specialist . This is a 06+ Months Contract opportunity with long-term potential and is located in Summit, NJ (Onsite). Please review the job description below and contact me ASAP if you...
Rees Scientific CorporatiMurfreesboro
Department: Service
Reports To: Regional Service Manager
Payroll Type: Salary
FLSA Status: Non-Exempt
Job Summary:
As a System Validation Specialist, you have hands on experience with installing, troubleshooting, repairing, calibrating...
Integrated Resources, IncWarren (NJ)
Job Title: Validation Specialist
Job Location: Warren, NJ
Job Duration: 5 Months
Work Schedule: Mon - Fri, Business Hours
Job Description:
The Validation Specialist, Computerized Systems, is responsible for performing initial and routine...
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Contract: Process / Equipment Validation Specialist
Protocol Link, Inc. | Florida | protocollink.ninjagig.com |
Bachelor’s degree in engineering, science, or similar. Candidate must have a minimum of 5-8 years of experience with qualification, protocol generation and execution in FDA-regulated companies. Responsibilities will require performing manufacturing process and equipment qualification activities for a global oral solid dosage pharmaceutical company.
Key Skills:
• Knowledge and understanding of Pharmaceutical GxPs and excellent GMP documentation skills
• Must be high energy, self-directed and driven, and must be able to work independently or with little supervision with sense of urgency accomplishing each task assigned
• Ability to effectively interact with individuals at all levels
• Intermediate to advanced MS Word and Excel needed as well as TrackWise, SharePoint, and PDF creator software experience
• Excellent written and verbal communication skills
Key Skills:
• Knowledge and understanding of Pharmaceutical GxPs and excellent GMP documentation skills
• Must be high energy, self-directed and driven, and must be able to work independently or with little supervision with sense of urgency accomplishing each task assigned
• Ability to effectively interact with individuals at all levels
• Intermediate to advanced MS Word and Excel needed as well as TrackWise, SharePoint, and PDF creator software experience
• Excellent written and verbal communication skills