Search Results: 20,817 vacancies
...Job Title : Equipment Validation Engineer
Location : Summit, NJ, Local candidates only
Type: Contract
Overview
Leading Pharmaceutical company looking for an experienced Equipment Validation Engineer. Ideal candidates should have a minimum of 5 years experience...
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Contract work
Local area
Overview:
This position is responsible for Equipment and Sterilization Validation processes (i.e. included but not limited to Autoclave, SIP, tunnel, dry heat, and VHP studies), that supports commercial and new R&D drug development activities in support of the client...
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...time with the people we love. That's what makes us Roche.
The Opportunity:
* Oversees work groups which conduct equipment and Facility validation, planning and logistics and other routine activities. Is responsible for the accuracy, quality and timeliness of logistics...
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Work experience placement
Relocation
Job Description: Commissioning/Qualification Specialist/Validation
100% Onsite Warren, NJLocal candidates only
Work Schedule: Mon... ...of cGMP pertaining pharmaceutical facilities, utilities, and equipment.
•Intermediate knowledge of pharmaceutical manufacturing and...
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Temporary work
Immediate start
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 are interested.
Job...
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Permanent employment
Contract work
Work experience placement
Local area
Immediate start
...power of business to build a better world.
Job Description:
Validation Engineer
Who You'll Work With
You will join one of our 4... ...FDA compliance related documents/protocols for pharmaceutical equipment. This person will travel to top clients across the country to...
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Flexible hours
...Validation Lead Location: Peapack, NJ Job Description: Strong Validation experience, Team lead and work experience in Agile is must Life Science validation experience TIBCO experience good to have Experience in working in fast paced Agile environment Validation, Technology...
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Work experience placement
...Responsibilities:
Primarily responsible for the support and execution of laboratory equipment qualification and associated computer system validation activities in compliance with current cGMP regulations and client's corporate principles, quality policies...
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VALIDATION ENGINEERS - Intellectt, Inc - Iselin, NJ Iselin, NJ & various unanticipated locations throughout the U.S: Mng spec, qualfctn & valdtn rqmts. Write & exec engg chng orders rltd to Corrective & Preventive Actions (CAPAs), chngs in Critical to Qlty (CTQs), release...
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...Schedule, plan, communicate, and manage documents and follow-up on validation activities. Interpret and apply regulatory requirements... ...Perform validation activities to lead and/or support cleaning, equipment, computer systems, utility, facility, and method validations....
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For contractors
....
3-5 years experience of Quality Assurance experience in the Pharmaceutical/Biotech Industry.
Experience in the use of validated computer systems for the management of regulated documents and training, including electronic records and electronic signatures....
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Our Process Validation Engineer plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products.... ...Engages with Engineering, Quality, and Operations to ensure equipment and manufacturing processes are appropriately designed to ensure...
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Holiday work
Full time
Work visa
...with manager and be available onsite when manager requests)
6 months Contract
The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy...
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Permanent employment
Contract work
Work experience placement
...Facilities Validation Engineer
The Validation Engineer is responsible for completing assigned equipment validation, packaging validation, computers validation, cleaning validation, and process areas to meet cGMP requirements.
Job Function...
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VALIDATION ENGINEERS - United Pharma Technologies, Inc. - South Plainfield, NJ So. Plainfield, NJ & other unantcptd locns nationwide. Duties: Analyze validation test data to determine whether systems or processes have met validation criteria & to identify root causes of...
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Temporary work
...Senior Validation Specialist
Warren, NJ--Onsite
Work Schedule: Mon - Fri, Business Hours
The Senior Validation Specialist, Computerized Systems, is responsible for performing initial and routine validation activities for GxP computerized systems. Primary responsibilities...
Work experience placement
...supervision, MV Scientists:
•Perform testing, analytical method validation and transfer activities of raw materials, in process (IP) and... ...experience in setting up and operating any/all of following equipment: LC-MS, GC, GC-MS, ICP-MS.
•Hands-on experience in setting...
Immediate start
...Responsibilities:
Lead and manage multiple commissioning / qualification / validation activities performed at facility with minimal supervision.
Equipment Qualification / Re-Qualification (IQ, OQ, PQ) for process equipment, QC equipment,...
For contractors
Internship
...Piper Companies is looking for an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Raritan, NJ area.
Responsibilities for the Analytical Validation Engineer include:
Experience...
Holiday work
...well as other research areas centered around rare diseases and immune disorders.
Summary
Manage Global DX Computer System Validation (CSV) projects within Daiichi Sankyo, for Computerized Systems supporting GxP and Non-GxP activities, assuring that these systems...
For contractors
