quality validation engineer - Chesterbrook, PA

We are looking for professionals with the required skills to achieve our goals: · Bachelor's degree in Mechanical, Electrical or Chemical Engineering, or BS/BA in a related scientific discipline (e.g. Chemistry, Biology). · 5+ years of relevant technical experience in a validati ...

As a Validation Engineer - Project Leader, working within the Clinical Sterile Operations pilot plant, you will be responsible for the successful delivery of validation life-cycle documents associated with direct impact clinical GMP manufacturing process equipment. · ...

The Quality Validation Engineer is responsible for ensuring that the company's proprietary work order system is designed, implemented, maintained, and controlled in compliance with applicable regulatory and quality standards, · System Validation & Compliance: Conduct systematic e ...

A Validation Engineer - Project Leader responsible for delivering validation life-cycle documents associated with clinical GMP manufacturing process equipment. · ...

The Quality Validation Engineer is responsible for ensuring that the company's proprietary work order system is designed, implemented, maintained, and controlled in compliance with applicable regulatory and quality standards. · ...

This role will provide YOU the opportunity to lead key activities to progress YOUR career. · ...

This role will provide YOU the opportunity to lead key activities to progress YOUR career. · ...

The ideal candidate is a recent engineering graduate with an interest in automation and control systems used in life sciences manufacturing (vaccines, biologics, cell and gene therapy). · Recent college degree in engineering with an interest in control systems testing. · Prefera ...

++The ideal candidate is a recent engineering graduate with an interest in automation and control systems used in life sciences manufacturing vaccines biologics cell gene therapy Experience as a Co Op or Intern in life sciences chemical or industrial engineering energy or manufac ...

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. · ...

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. · The ultimate goal of a Valspec validation engineer is to test computer systems that manufacture phar ...

We are looking for tech savvy professionals with a proven track record in the SDLC (system development life cycle) of automated computer systems within biopharmaceutical environments. · ...

The Quality Validation Engineer is responsible for ensuring that the company's proprietary work order system is designed, implemented, maintained, · and controlled in compliance with applicable regulatory and quality standards. · Conduct systematic evaluations of digital system w ...

The ideal candidate is a recent engineering graduate with an interest in automation and control systems used in life sciences manufacturing vaccines biologics cell and gene therapy Experience as a Co-Op or Intern in life sciences chemical or industrial engineering energy or manuf ...

Job summary · Validation Engineer at Valspec · Qualifications3+ years of Computer System Validation (CSV) experience with process control, SCADA and automation systems, MES and data integration systems (Emerson DeltaV and/or Syncade experience is highly preferred) · ...

SOKOL GxP Services is seeking an experienced and detail-oriented Validation Engineer to support temperature and environmental mapping activities for GMP-controlled spaces, equipment, and utilities. · ...

SOKOL GxP Services is seeking an experienced and detail-oriented Validation Engineer to support temperature and environmental mapping activities for GMP-controlled spaces, equipment, and utilities. · ...

SOKOL GxP Services is seeking an experienced and detail-oriented Validation Engineer to support temperature and environmental mapping activities for GMP-controlled spaces equipment and utilities while also contributing to general Commissioning Qualification and Validation CQV act ...

+ Execute CSA and validation activities in accordance with SDLC procedures and quality expectations · + Assist in preparation of validation plans, functional risk assessments, · and traceability matrices. · High growth potential and fast-paced organization with a people-focused c ...

Verista's team of experts work with the world's most recognizable brands in the life science industry to solve their business needs. · ...