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  • Employer: Katalyst HealthCares And Life Sciences (undo)

Katalyst HealthCares And Life Sciences Jobs
Jobs 1 to 11 of 11

Katalyst HealthCares And Life Sciences Jobs

Jobs 1 to 11 of 11

Marlborough, Massachusetts

Responsibilities: Collaborates with business leaders and/or Program owners to support the identification and prioritization of programs/projects that advance strategic initiatives and translate...

2016-12-01Today
Houston, Texas

Responsibilities: Coordinate, evaluate, and follow patient progress while on studies maintaining knowledge of adverse events, protocol-related labs and research tests, and protocol responses....

2016-12-01Today
Marlborough, Massachusetts

Responsibilities: Collaborates with business leaders and/or Program owners to support the identification and prioritization of programs/projects that advance strategic initiatives and translate...

2016-12-01Today
Houston, Texas

Responsibilities: Coordinate, evaluate, and follow patient progress while on studies maintaining knowledge of adverse events, protocol-related labs and research tests, and protocol responses....

2016-12-01Today
Wilson, North Carolina

Responsibilities: Perform all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures. ccurately document all necessary and relevant...

2016-12-01Today
Redwood City, California

Responsibilities: Act as the study lead delegate on cross-functional study teams, Vendor, and CRO operational meetings and ensure compliance with global operational standards and procedures....

2016-12-01Today
South Plainfield, New Jersey

Roles and Responsibilities: Collaborate with cross-functional teams to establish quality and performance metrics for suppliers. Establish regular connects with supplier to evaluate Material changes...

2016-12-01Yesterday
Wilson, North Carolina

Responsibilities: Perform all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures. ccurately document all necessary and relevant...

2016-12-01Yesterday
Tucson, Arizona

Responsibilities: Responsible for designing and implementing manufacturing processes which are compliant with FDA/ISO Quality Systems regulations for Medical Devices. Familiar with a variety of...

2016-12-012 days ago
Apex, North Carolina

Quality Engineer (Contract)Location: Apex, NCJob Description (primary responsibilities) Conducting product and process audits to identify areas for improvement Developing and implementing quality...

2016-12-012 days ago
Belmont, California

Responsibilities: Bachelor's degree in chemistry with 2-year R&D experience in Medical Device and Biotechnology Industry. Experience in Organic Synthesis, Polymer Chemistry, Raw Material...

2016-12-012 days ago
San Diego, California

Responsibilities: Conduct single or multi-center medical device clinical studies. Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action...

2016-12-013 days ago
Wilson, North Carolina

Responsibilities: Perform all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures. ccurately document all necessary and relevant...

2016-12-01Today
Redwood City, California

Responsibilities: Act as the study lead delegate on cross-functional study teams, Vendor, and CRO operational meetings and ensure compliance with global operational standards and procedures....

2016-12-01Today
South Plainfield, New Jersey

Roles and Responsibilities: Collaborate with cross-functional teams to establish quality and performance metrics for suppliers. Establish regular connects with supplier to evaluate Material changes...

2016-12-01Yesterday
Wilson, North Carolina

Responsibilities: Perform all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures. ccurately document all necessary and relevant...

2016-12-01Yesterday
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