The Validation Engineer II is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes...

The Validation Engineer II is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes...

Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls. Ability to follow oral and written instru...

Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, and Change Controls. Supports the execution of equipment q...

Validation Engineer 6 years, Validation Engineer 3 years. Execute validation protocols, write validation reports. Experience in drug/biologics industry in GMP production environment in roles of valida...

Job Title: MES Validation Engineer. We are seeking a dedicated professional to take ownership of computer system validation activities for Manufacturing Execution Systems supporting cell therapy manuf...

Collaborate cross-functionally with device engineers, laboratory teams, and quality departments to ensure alignment and successful execution of test method validation (TMV) activities. Support regulat...

Generation of qualification / validation documents, execution of qualification / validation documents, generation of reports, adhering to project timelines, ensure compliance with company and industry...

Support validation activities for project activities including review of validation documentation (FAT, SAT, URS, SDS, IQ, OQ, PQ) and attendance at validation activities. Manufacturing, Validation, S...

Keywords: commissioning, qualification, decommissioning, production, validation standards, validation criteria, procedures, protocol, validation test equipment, detail-oriented, quality assurance, inn...

Support validation activities for project activities including review of validation documentation (FAT, SAT, URS, SDS, IQ, OQ, PQ) and attendance at validation activities. Ensuring appropriate investi...

The Validation Engineer supports the successful implementation of laboratory equipment and systems at multi-use sites through interaction with internal customers and external service providers. Excell...

The Senior Software Validation Engineer will be an on-site role reporting into Trumbull, Connecticut and will be responsible for providing software design and implementation support for Quality Engine...

Support and address comments and suggestions associated with validation and engineering documentation. Qualified candidates must be experienced in one or more of the following areas of validation:. Ge...

Software Quality Engineering and/or Computer System Validation (CSV). We are seeking an innovative and highly motivated Computer System Validation (CSV) Engineer who will be part of Cellares' Quality ...

Excellent technical writing skills and proficiency with Microsoft Word formatting functions; ability to efficiently create technically accurate documents for system lifecycle deliverables in alignment...

Lead and execute validation plans for analytical system updates and process improvements. Manage validation-related records such as Change Controls (CC), CAPAs, and Deviations using TrackWise. Review ...

Please find below the job description for the.Secure boot, secure update, security features for embedded systems, security in embedded not cloud side -experience in verification of Security features l...

Lead and execute validation plans for analytical system updates and process improvements. Manage validation-related records such as Change Controls (CC), CAPAs, and Deviations using TrackWise. Review ...

Excellent technical writing skills and proficiency with Microsoft Word formatting functions; ability to efficiently create technically accurate documents for system lifecycle deliverables in alignment...

Full lifecycle validation for all applicable computerized systems, ensuring they are designed, validated, operated and retired in compliance with GxP regulation and computer system validation (CSV) gu...

Roles & Responsibilities: Develop and execute validation protocols for computer systems. Create detailed validation documentation including plans, reports, and scripts. Collaborate with cross-functio...

Write and execute validation documents, including Validation Plans, URS, IQ/OQ/PQ protocols, traceability matrices, and summary reports. Lead or support engineering studies for process parameter defin...

Draft and execute key validation documents including validation plans, user requirements, IQ/OQ/PQ protocols, RTMs, VSRs, and change control documentation. Design and run engineering studies to define...

Write and execute validation documents, including Validation Plans, URS, IQ/OQ/PQ protocols, traceability matrices, and summary reports. Lead or support engineering studies for process parameter defin...

Minimum 3-years’ experience of working on manufacturing engineering validation activities. HCLTech is looking for a highly talented and self- motivated Process Validation Engineer to join it in advanc...

Minimum 3-years’ experience of working on manufacturing engineering validation activities. HCLTech is looking for a highly talented and self- motivated Process Validation Engineer to join it in advanc...

Design and run engineering studies to define and verify critical process parameters prior to system validation. Draft and execute key validation documents including validation plans, user requirements...

Our client is actively looking for a Validation Engineer II and III. Experience with CQV, sterilization validation and cleaning validation. Scientific or Engineering related discipline.

Our client is actively looking for a Validation Engineer II and III. Experience with CQV, sterilization validation and cleaning validation. Scientific or Engineering related discipline.

Support validation activities for project activities including review of validation documentation (FAT, SAT, URS, SDS, IQ, OQ, PQ) and attendance at validation activities. Employee will be required to...

Support validation activities for project activities including review of validation documentation (FAT, SAT, URS, SDS, IQ, OQ, PQ) and attendance at validation activities. Employee will be required to...

Coordinate all validation processes regarding validation programs and schedules with customers in collaboration with Business Operations, Scheduling, Engineering, and QA. The Validation Engineer ensur...

Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls. Ability to follow oral and written instru...

Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls. Required BS degree in Engineering / Compu...

Our client is actively looking for a Validation Engineer II and III. Experience with CQV, sterilization validation and cleaning validation. Scientific or Engineering related discipline.

Our client is actively looking for a Validation Engineer II and III. Experience with CQV, sterilization validation and cleaning validation. Scientific or Engineering related discipline.

Responsibilities of the Senior Validation Engineer include:. Qualifications for the Senior Validation Engineer include:. Compensation for the Senior Validation Engineer include:.

Compensation for the Validation Engineer (CSV/CQV). Responsibilities for the Validation Engineer (CSV/CQV). Qualifications for the Validation Engineer (CSV/CQV).

Must have excellent communication skills and be comfortable presenting the validation results to our customer's project team (QA, validation, project management, etc. Description Acara Solutions is se...