5823 - Validation Engineer / CQV Engineer - Indianapolis

+Job summary · Ensure operational readiness for biotech innovators. Develop and maintain user requirement specifications. · +Develop and maintain user requirement specifications. · Author IOQ protocols and assist with PQ planning. · + · ...

Piper Companies is seeking a CQV Engineer to join a leading organization focused on ensuring operational readiness for biotech innovators. · This role requires strong expertise in aseptic fill lines and the ability to work independently in a fast-paced environment. · ...

Piper Companies is seeking a CQV Engineer to join a leading organization focused on ensuring operational readiness for biotech innovators. · ...

Support a greenfield pharmaceutical facility through documentation build-out, commissioning, and qualification. · ...

Support a greenfield pharmaceutical facility through documentation build-out, commissioning, and qualification. · ...

We empower growth and innovation within the scientific community and help researchers solve some of the world's most pressing healthcare challenges. · ...

We at Eliquent are looking for an experienced Validation Engineer to immediately join our Indianapolis team. The Validation Engineer is responsible for the theory and content of validation documents for new cleanrooms and packaging equipment, · Eliquent Life Sciences is proud to ...

We are looking for a passionate Senior Commissioning, Qualification, and Validation (CQV) Engineer who is driven by collaboration, exceeding expectations, and challenging the status quo. · As a Senior CQV Engineer you'll join our collaborative team providing CQV support to client ...

The Filling CQV Engineer Jr will join a leading global pharmaceutical company that is rapidly expanding its international presence and support a Manufacturing Facility in Indianapolis. ...

The Filling CQV Engineer Sr will join a leading global pharmaceutical company that is rapidly expanding its international presence, · This role supports a Manufacturing Facility in Indianapolis Indiana and focuses on commissioning qualification and validation of aseptic filling e ...

The Filling CQV Engineer Sr will join a leading global pharmaceutical company that is rapidly expanding its international presence.This role supports a Manufacturing Facility in Indianapolis and focuses on commissioning qualification and validation of aseptic filling equipment. · ...

+The Filling CQV Engineer Jr will join a leading global pharmaceutical company that is rapidly expanding its international presence. This role supports a Manufacturing Facility in Indianapolis, Indiana. · +CQV & Protocol Development: · Support CQV of a Cytiva Aseptic Filler. · Ex ...

We are hiring a Commissioning/Qualification/Validation Project Engineer to deliver new and modified systems that are safe, functional, and compliant with design requirements and regulations. · ...

The Lead CQV Engineer will be responsible for lead commissioning, qualification and validation (CQV) efforts for a greenfield API manufacturing project. · ...

Piper Companies is hiring a skilled Lead CQV Engineer for an onsite contract position based out of Lebanon, IN. The Lead CQV Engineer will be responsible for lead commissioning, qualification and validation efforts for a greenfield API manufacturing project focusing on downstream ...

Verista is seeking a detail-oriented Validation / CQV Engineer with strong experience in change management and documentation control within regulated pharmaceutical manufacturing environments. · Support commissioning qualification validation activities for laboratory and manufact ...

Job summary · Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. · ResponsibilitiesSupport commissioning, qualification, and validation (CQV) activities for laboratory and manufacturing systems withi ...

Verista is seeking a detail-oriented Validation / CQV Engineer with strong experience in change management and documentation control within regulated pharmaceutical manufacturing environments.This role supports commissioning, qualification, validation, and lifecycle change activi ...

Verista's team of experts works with life science companies to solve their business needs. We empower growth and innovation within the scientific community by providing innovative solutions and services that enable informed decision-making() · Support commissioning, qualification ...

Verista is seeking a detail-oriented Validation / CQV Engineer with strong experience in change management and documentation control within regulated pharmaceutical manufacturing environments. · ...