Validation Engineering Group Inc Jobs October 2024

The management jobs sector in the UK offers a diverse range of opportunities for professionals looking to lead and innovate across various industries. With roles spanning from project management to executive leadership, this dynamic field is essential for driving business success and organisational growth. As companies continue to evolve, the demand for skilled managers who can navigate complex challenges and implement effective strategies remains high. Explore our latest management job listings to find your next career move and become a key player in shaping the future of your industry.

177617 Jobs Found for Validation Engineering Group Inc

£150 - £200 Per Annum

KNZA, INC is a growing and aggressive company that is looking to add to our current team. Our group of five locally owned radio stations is now taking applications for a General Manager. This is a newly created full-time position for a visionary leader that is experienced and passionate about broadcasting, thrives in a fast-paced environment, and h...

Position Summary The Sr. Accountant will perform a variety of general accounting tasks in the Accounting Department and work collectively with team members in order to meet and exceed service expectations. Essential Functions Analyze financial information detailing assets, liabilities, and capital Compile and analyze financial information to prep...

Impact Evaluation Director (GS-12) Position Location: Denver, Colorado or Washington D.C 1. Summary Causal Design is an economic consulting firm conducting rigorous program evaluations and analysis for international development organizations. Our evaluations are designed to provide timely and practical information to decision makers working to...

• 10+ years' experience in Computer System Validation or Quality management or Business Analysis in GxP application area • Has working experience in any one or two of the following domains - Clinical Development and Supply Chain, Drug Discovery, MES, QMS, LIMS, Data Integrity Platforms • Guide the project team with the right set of applicable proje...

• 10+ years' experience in Computer System Validation or Quality management or Business Analysis in GxP application area • Has working experience in any one or two of the following domains - Clinical Development and Supply Chain, Drug Discovery, MES, QMS, LIMS, Data Integrity Platforms • Guide the project team with the right set of applicable proje...

Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transfor...

£125 - £150 Per Annum

Req ID: 299676 NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now. We are currently seeking a Senior Project Manager -GxP Validation to join our team in Kalamazoo, Michigan (US-MI), United States (US). ...

£100 - £125 Per Annum

Raritan, United States | Posted on 07/15/2024 Industry: Pharma/Biotech/Clinical Research Work Experience: 5+ years City: Raritan State/Province: New Jersey Country: United States Job Description A Computer System Validation (CSV) Lead is responsible for ensuring that all computer systems and software used within a company, particularly...

£150 - £200 Per Annum

Summary Posted: May 14, 2024 Weekly Hours: 40 Role Number: 200550434 Hardware Engineering is looking for a system hardware validation engineer to develop new hardware test plans, test execution and validation of hardware designed for large scale deployment and integrated use. This ranges from validation of individual systems through that of mult...

Responsibilities: Serve as QA electronic system validation expert and will provide oversight and guidance on computer systems validation in accordance with applicable regulations, guidelines, policies and procedures. Train, support and advise end users on EDMS and QMS system requirements and workflows. Manage the GMP document life-cycle management ...

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