Validation Engineer - Andover, MA

The Instrument Validation Specialist will support a diverse variety of Quality Control and Manufacturing Instrumentation. · ...

Provide validation support related to qualification of manufacturing processes and equipment within a biopharmaceutical manufacturing facility including shipping validation process validation equipment qualification cleaning validation sterilization and dry heat qualification. · ...

Provide validation support related to qualification of manufacturing processes and equipment within a biopharmaceutical manufacturing facility. · ...

The qualified candidate must have the experience and ability to participate in multiple projects within Site Technical Services (STS), Quality Control (QC), Quality Assurance (QA), Quality Laboratory Systems (QLS) and Business Technology (BT). Performs all work in compliance with ...

The Instrument Validation Specialist will support a diverse variety of Quality Control and Manufacturing Instrumentation. · Authoring validation documentation for analytical and microbiology instrumentation · PARTICIPATING in Data Integrity and Electronic Records and Electronic S ...

The individual will provide Quality Assurance oversight in support of a site product enabling engineering project. · The individual will be responsible for the quality review and approval of validation and change control documentation. · Ensure compliance to governing SOPs, valid ...

The Process Validation Engineer will be responsible for developing, executing and maintaining validation activities for pharmaceutical manufacturing processes with a primary focus on Skid filtration systems and Change Control management.This role ensures compliance with regulator ...

Join my client's cutting-edge radiopharmaceutical manufacturing operation and play a pivotal role in bringing life-changing therapies to patients. · This is your opportunity to shape compliant inspection-ready systems from the ground up in a rapidly advancing sector of biotech. · ...

The Process Validation Engineer will be responsible for developing, executing and maintaining validation activities for pharmaceutical manufacturing processes. · ...

The Instrument Validation Specialist will support a diverse variety of Quality Control and Manufacturing Instrumentation including analytical and microbiological instruments maintaining the validated state of the instruments from implementation through their full lifecycle.This r ...

The Instrument Validation Specialist will support Quality Control and Manufacturing Instrumentation. · ResponsibilitiesAuthoring validation documentation (validation plans, requirement specifications) · Execution of qualification protocols · ...

The individual will provide Quality Assurance oversight in support of a site product enabling engineering project. · The documentation will span the breadth of validation and change control requirements for biopharmaceutical processing and Quality Control (QC) instruments. · Ensu ...

The GMP Liquid Dose Manufacturing (LDM) implements and maintains various equipment systems in support of the manufacture of clinical biologic drug products. · Manage the qualification effort i.e. coordination of materials and equipment · Generate all necessary electronic protocol ...

The individual will be responsible for the quality review and approval of validation and change control documentation such as protocols test plans various computer validation testing documents deviations and change controls in relation to DI remediation activities.The documentati ...

The individual will be responsible for the quality review and approval of validation and change control documentation such as protocols, test plans, various computer validation testing documents, deviations, · and change controls in relation to DI remediation activities.The docum ...

The individual will provide Quality Assurance oversight in support of a site product enabling engineering project. · ...

The Process Validation Engineer will be responsible for developing, executing, and maintaining validation activities for pharmaceutical manufacturing processes, · Develop and execute validation protocols (IQ/OQ/PQ) for Skid filtration systems and associated equipment. · Perform r ...

We are excited about the opportunity to work with you and glad you want to be part of a team of talented individuals who together are changing the way the world communicates. · You will learn and participate in developing advanced, state-of-the-art RF front-end modules · You will ...

We're hiring If you want your contributions to make a real difference check out this new career opportunity with us at Draeger where we are guided by the principle Technology for Life. · Review and feedback of testability of product requirements. · Design and develop test strateg ...

Want to join a team that provides cutting-edge solutions for world-class projects? Infineon is made up of passionate, smart, energetic people who will challenge and inspire you every day. · ...