19 matches found.
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Senior Data Manager
Union County, New Jersey
Senior Data Manager
Responsibilities:
- Manage clinical trial databases:
- Review protocols for proper data capture including case report form design and CRF completion instructions
-...
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Senior Compliance Specialist
Union County, New Jersey
Senior Compliance Specialist
Compliance Management
- Performs audits of processes, departments, and systems, internally and externally (travel required) verses the Company's Standards and applic...
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Quality Tech
Irvine, California
Quality Technician recieves, collects and analyzes appropriate samples for the release testing of raw materials, maitain protocols, final reports, reserve samples, product complaints, and batch record...
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Senior Quality Engineer/Quality Engineer
Mid-Southern Atlantic region
Working individually or in a team environment identifies and puts into place corrective actions to address potential or actual process failures (equipment, procedural, people or materials). The key ro...
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Quality Assurance & Regulatory Affairs Manager
Gainesville, Florida
My client a manufacturer in the vicinity of Gainesville, FL is seeking an experienced Manager of Quality Assurance and Regulatory Affairs for a two site location. The primary responsibility of this po...
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Manager, Quality Auditing
Hudson Valley, New York
REQUIREMENTS:
Bachelor's degree in Science or related field from an accredited college or university, and 7+ years pharmaceutical quality assurance experience, or an equivalent combination of educa...
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Technical Writer
Miami, Florida
job description
Join a leading pharmaceutical company, marketing products from a wide range of therapeutic areas including analgesic, anti-infective, cardiovascular, on...
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Quality Control Associate
Connecticut
Provide assistance to the Drug Safety Systems Validation Manager with creation of test plans, execution of test cases and coordination of validation documentation in support of the enhancement of data...
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Technical Writer
Miami, Florida
job description
Join a leading pharmaceutical company, marketing products from a wide range of therapeutic areas including analgesic, anti-infective, cardiovascular, on...
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Quality Tech
Irvine, California
Quality Technician recieves, collects and analyzes appropriate samples for the release testing of raw materials, maitain protocols, final reports, reserve samples, product complaints, and batch record...
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Validation Specialist
Memphis, Tennessee
Summary Description
Responsibilities include the planning, coordination and execution of validation studies. You will conduct and document validation studies of equipment according to written proto...
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Senior Data Manager
Union County, New Jersey
Senior Data Manager
Responsibilities:
- Manage clinical trial databases:
- Review protocols for proper data capture including case report form design and CRF completion instructions
-...
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Validation Specialist
Memphis, Tennessee
Summary Description
Responsibilities include the planning, coordination and execution of validation studies. You will conduct and document validation studies of equipment according to written proto...
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Senior Compliance Specialist
Union County, New Jersey
Senior Compliance Specialist
Compliance Management
- Performs audits of processes, departments, and systems, internally and externally (travel required) verses the Company's Standards and applic...
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Quality Control Associate
Connecticut
Provide assistance to the Drug Safety Systems Validation Manager with creation of test plans, execution of test cases and coordination of validation documentation in support of the enhancement of data...
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|
Quality Tech
Irvine, California
Quality Technician recieves, collects and analyzes appropriate samples for the release testing of raw materials, maitain protocols, final reports, reserve samples, product complaints, and batch record...
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Technical Writer
Miami, Florida
job description
Join a leading pharmaceutical company, marketing products from a wide range of therapeutic areas including analgesic, anti-infective, cardiovascular, on...
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QA Supervisor, Clinical Packaging
NY,NJ,CT.
QA Supervisor, Clinical Packaging
Description of Duties and Responsibilities:
• Supervise and Coordinate QA Process Daily Packaging Activities
- Perform both initial and/or secondary batch re...
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SR QA MANAGER
Boston area, Massachusetts
Ensuring adherence by company and 3rd party manufacturers to GMPs and applicable international standards and guidelines in support of commercial products and clinical trial materials will be the key r...
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