Search Results: 37,059 vacancies
Job Title : Validation Engineer
Location : Summit, NJ
Type: Contract
Responsibilities
Maintains qualified equipment systems in compliance with policies, guidelines and procedures:
Develops qualification pro...
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Contract work
...therapies in oncology, as 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...
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For contractors
...Job Title : Validation Engineer
Location : Summit, NJ
Type: Contract
Responsibilities
Maintains qualified equipment systems... ...protocols, and associated reports while adhering to a change management process.
Supports the execution of equipment qualifications...
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Contract work
...position
PURPOSE AND SCOPE OF POSITION:
The Equipment Validation Engineer supports the successful implementation of various... ...systems.
•Understanding of investigations, deviations and CAPA management in a regulated pharmaceutical industry.
•Strong written and...
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Immediate start
Work alone
...Job Description
Job: Validation Lead (CSV, Clinical Systems)
Location: NJ/PA(Hybrid)
Mandatory Skills: CSV, Computer System Validation... ...execution documents.
Perform all aspects of QMS (Quality Management System) processes (Change Control, Deviation, CAPA) as well as...
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Our Process Validation Engineer plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products.... ...Provides Quality Partners, Commercial Operations, and Executive Management visibility of shop floor concerns related to production...
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Holiday work
Full time
Work visa
...required
The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise... ..., CI Owners, Quality, and the global EMES team to create, manage, and improve computerized systems/Recipes validation deliverables...
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Permanent employment
Work experience placement
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Insight Global is seeking an experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full-time position. This position will be 5 days a week onsite, in Parsippany, NJ. This individual will play a crucial role in ensuring quality and...
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Full time
...Job Description
Job Description The Senior Validation Manager is leading the site validation program and all qualification and validation activities at the Erytech, Princeton site, NJ. Validation activities include Facility/Clean rooms, manufacturing equipment, laboratory...
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...openings in Monmouth Junction, NJ for MV Scientists.
Under supervision, MV Scientists:
•Perform testing, analytical method validation and transfer activities of raw materials, in process (IP) and finished products (FP) samples to support Technical Services (TS) submission...
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Immediate start
Immediate need for a talented Manufacturing Systems Validation Specialist . This is a 06+ Months Contract opportunity with long-term... ...Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods.
With advanced...
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Local area
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Job Title: Validation Engineer - Pharmaceutical
Job Summary:
The Validation Engineer is responsible for completing assigned job of... ...innovative cross functional synergies.
Excellent project management and problem solving skill
The requirement for English...
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Flexible hours
...Job Description
Job Description:
We are looking for a manager to lead and manage the validation and testing activities for our platform products. This role will need will collaborate with cross-functional teams, including development, product management, and quality...
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Holiday work
Full time
Remote job
Relocation
Visa sponsorship
Flexible hours
Shift work
3 days per week
...Job Title : Validation Specialist
Location : Warren, NJ
Hours/Schedule : Mon - Fri, Business Hours
Type: Contract
Responsibilities... ...Performs validation document generation, program management, and protocol execution activities.
Interface with Engineering...
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Work experience placement
...Job Description
Job Description Quality Assurance Manager (Compliance) Allendale, NJ The Manager, Quality Assurance manages the... ...software deployment, customer integration, and professional services validation.
The QA Manager will delegate responsibilities to direct...
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Flexible hours
...of 21 CFR Part 11, ICH standards, EMA and FDA (GxP) regulations, and GAMP methodologies
Coordinate with multi-disciplinary validation team and be responsible for the validation of automated equipment and control systems
Create and modify validation documentation...
...Job Description
Job Description Quality Assurance Manager - Validation Allendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device, IT and Human Resources disciplines in New Jersey. This position...
Holiday work
Flexible hours
Night shift
Weekend work
...Job Description
Job Description The Validation Specialist, Computerized Systems, is responsible for performing initial and routine validation activities for GxP computerized systems. Primary responsibilities include: qualification of laboratory instruments, setup...
Work experience placement
...opportunities within the scientific ladder, to pursue project management, or develop into a leaderthese are just a few career pathways... ...Group can advance your career, apply now!
The main focus of the Validation Analyst (also referred to as a Scientific Software Compliance...
Full time
Contract work
Local area
Work alone
...System project teams in the review and QA approval of system validation and infrastructure qualification documentation and protocols,... ...the subject matter expert.
Present project status reports to management as well as project teams.
Review Change Control requests and...
For contractors
Immediate start
