Computer Systems Validation Engineer - Rockville, MD

We are seeking a Validation Engineer to join our team. The ideal candidate will have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities and equipment qualifications process ...

We are seeking a Validation Engineer II to join our team. The ideal candidate will have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, pro ...

The Validation Engineer I supports activities within the Drug Delivery Sciences department related to process development validation and technology transfer. · ...

This is a hands-on, non-supervisory role within the Central Laboratory Operations (CLO) department of the Global Laboratory and Technical Operations (GLTO) division. · The incumbent will execute and support routine validation activities, ensuring compliance with USP standards, re ...

We are seeking a Cleaning Validation Engineer to support our teams of industry subject matter experts and thought leaders in the pharmaceutical, biotechnology, and medical device industries. · ...

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We offers validation and quality expertise to the pharmaceutical and biotechnology industries. · The validation specialist will evaluate equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach ...

This hands-on role within Central Laboratory Operations executes routine validation activities ensuring compliance with USP standards regulatory requirements and industry best practices. ...

The Associate Validation Engineer role at USP involves executing and supporting routine validation activities to ensure compliance with USP standards, regulatory requirements, and industry best practices. The incumbent will work closely with laboratory staff in executing validati ...

This is an Associate Validation Engineer position at USP in Rockville Maryland US working on validation activities ensuring compliance with USP standards regulatory requirements industry best practices providing technical support to metrology operations assisting in instrument ca ...

We are seeking a Cleaning Validation Engineer to work on-site at our client's biotech facility in the Bethesda, MD area. · ...

+This is a hands-on, non-supervisory role within the Central Laboratory Operations (CLO) department of the Global Laboratory and Technical Operations (GLTO) division. · +Work closely with laboratory staff in executing validation, metrology, and calibration activities. · Support e ...

pBAE Systems is seeking a full-time Principal Verification and Validation Engineer to support our work as a prime contractor on a high-profile U.S. · Navy weapon system./p/h2/ · The ideal candidate would be self-motivated, good at planning, · and have excellent written · & · verb ...

BAE Systems is seeking a full-time Principal Verification and Validation Engineer to support our work as a prime contractor on a high-profile U.S. Navy weapon system. · ...

+Job summary · This position is responsible for providing quality assurance that software used to support MSD manufacturing processes, analytical services, and quality management systems is validated, · ResponsibilitiesSupport Computerized System Validation (CSV) activities acros ...

Job DescriptionThe candidate needs to have current industry Cleaning Validation knowledge, including autoclaves for drug products. · 5+ years of Cleaning Validation experience in Biotech/Biologics/Pharma industries. · ...

We are currently hiring for a EMPQ Validation Engineer to support a global biologics manufacturer during a critical qualification phase. · The focus is execution, data generation, and documentation. · This opportunity is well suited for a validation or QC professional looking to ...

Execute Computer System Validation (CSV) activities for GMP manufacturing systems. · Validate computerized systems associated with bioprocess manufacturing equipment. · ...

We are seeking an experienced Validation Engineer with strong EMPQ expertise to support a new facility startup. This role will focus on protocol development, execution, and documentation for facility and equipment qualification activities.Develop and execute EMPQ protocols includ ...

The client has an established commissioning and validation strategy with all SOPs and requirements defined. They need additional hands-on execution support for a critical gap: performing risk-based assessments during commissioning and translating that work into a defensible valid ...