Filling CQV Engineer Sr - Indianapolis, IN
1 month ago
Job summary
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 equipment.
The engineer will be responsible for protocol development IOQ execution and airflow testing contributing to a high-performing team with a strong track record of success.
- Collaborate with subject matter experts to ensure all inputs are captured for comprehensive protocol creation.
- Maintain high standards of quality compliance and execution in a regulated environment.
- Participate in continuous improvement initiatives and support site operations.
Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
CQV Engineer
5 days ago
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. · ...
CQV Engineer
1 month ago
+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. · + · ...
CQV Engineer
3 weeks ago
Support a greenfield pharmaceutical facility through documentation build-out, commissioning, and qualification. · ...
CQV Engineer
1 month ago
Piper Companies is seeking a CQV Engineer to join a leading organization focused on ensuring operational readiness for biotech innovators. · ...
CQV Engineer
3 weeks ago
Support a greenfield pharmaceutical facility through documentation build-out, commissioning, and qualification. · ...
CQV Engineer
4 days ago
We empower growth and innovation within the scientific community and help researchers solve some of the world's most pressing healthcare challenges. · ...
CQV Engineer
1 month ago
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 ...
Senior CQV Engineer
4 days ago
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 ...
Filling CQV Engineer Jr
1 month ago
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. ...
Filling CQV Engineer Sr
1 month ago
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. · ...
Filling CQV Engineer Jr
3 weeks ago
+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 ...
5823 - Validation Engineer / CQV Engineer
1 month ago
We empower and support our colleagues · We commit to client success at every turn · We have the courage to do the right thing · We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged. · ...
Commissioning CQV Project Engineer I
4 days ago
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. · ...
Lead CQV Engineer
1 month ago
The Lead CQV Engineer will be responsible for lead commissioning, qualification and validation (CQV) efforts for a greenfield API manufacturing project. · ...
Lead CQV Engineer
1 month ago
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 ...
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. · Support commissioning qualification validation activities for laboratory and manufact ...
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. · ...