Validation Specialist - Marlborough, MA

Kelly Science is seeking a Validation Engineer for a growing company located in Marlborough. · ...

This is a hands on position responsible for authoring test scripts and other CSV documents required for the validation of GAMP 5 Category 4 configurable off the shelf computer systems. · Createand/or review computer system validation test scripts, validation schedules, risk asses ...

We are seeking a Computer Validation Specialist to join our team. This position involves writing CSV test scripts, protocols, and summary reports in global environments. · ...

The Analytical Quality & Compliance Specialist will focus on QA review and approval of technical documents pertaining to GMP analytical methods for biologics drug substances and drug products. · Analytical method validation protocols and reports for in process, release, and stabi ...

Perform validation (IQ, OQ, PQ) of various types of equipment and systems including validation or requalification of temperature controlled chambers and lab equipment. · ...

· This role requires a Validation Specialist with strong skills in risk assessment and protocol generation to ensure the shipping and transport validation processes are executed flawlessly. · ...

The CDI Validation Specialist assists the CDI Manager with oversight evaluation and analysis of CDI functions including efficiency accuracy continuing education needs and overall quality. · The individual identifies individual education needs of Clinical Documentation Specialists ...

The CDI Validation Specialist assists with oversight evaluation analysis of CDI functions including efficiency accuracy continuing education needs overall quality. · ...

+Job summary · The CDI Validation Specialist assists the CDI Manager with oversight evaluation and analysis of CDI functions including efficiency accuracy continuing education needs and overall quality. · This individual identifies individual education needs of Clinical Documenta ...

The CDI Validation Specialist assists with oversight evaluation analysis of CDI functions including efficiency accuracy continuing education needs overall quality. · Monitors CDI staff accuracy data quality integrity. · Audits clinical documentation specialists retrospectively to ...

We are seeking an IT Validation Specialist to join our team at Net2Source Inc. The successful candidate will be responsible for providing application validation support, documentation, training, and troubleshooting of Veeva systems. · Knowledge of science biology, chemistry, engi ...

+The CDI Validation Specialist assists the CDI Manager with oversight, evaluation, · and analysis of CDI functions including efficiency, · accuracy, · continuing education needs, · and overall quality. · +Bachelor's degree (or equivalent) in nursing, · health information manageme ...

We're hiring a Data Validation Specialist to review contractor-submitted documentation and ensure it's entered with precision and care. · This role is key to reviewing safety and financial documents submitted by contractors, including income statements, balance sheets, and insura ...

+The position is responsible for qualifying analytical and microbiological testing instrumentation for the company. · The goal is to efficiently specify/source laboratory equipment and execute qualifications in a timely manner to enable QC Microbiology and QC Chemistry department ...

The Validation Specialist III will be responsible for the management and implementation of the Laboratory Equipment Qualification system. · Coordinate activities relating to the qualification, calibration and maintenance of laboratory equipment and related systems. · ...

The Senior Validation Specialist will support a diverse variety of qualification activities for manufacturing processes and equipment within a biopharmaceutical manufacturing facility. · ...

The Senior Validation Specialist 1 will support a diverse variety of qualification activities for manufacturing processes and equipment within a biopharmaceutical manufacturing facility. · The role will also provide technical support for continuous improvement projects. · ...

This is an exciting opportunity to join Bristol Myers Squibb as a Validation Engineer I. As part of our team, you will play an integral role in supporting the successful implementation of manufacturing and laboratory equipment at multi-use sites. · ...

The Specialist, · Validation · Engineer I supports the successful implementation of manufacturing, · and laboratory equipment alongside facilities · Maintains qualified equipment systems in compliance with policies, · Develops and executes validation/qualification deliverables su ...

The Specialist, Validation Engineer I supports the successful implementation of manufacturing, · and laboratory equipment alongside facilities and utilities at multi-use sites through interaction with internal customers · and external service providers. · ...