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Director of Audit and Inspection for Quality Assurance (GCP/GPvP

AstraZeneca Pharmaceuticals Gaithersburg
Description: At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We con...
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Senior Quality Engineer

AstraZeneca Pharmaceuticals Boulder
Description MedImmune is the worldwide biologics research and development arm of AstraZeneca. Here, you’ll have the opportunity to make a difference in people’s lives every day. As one of the world’s premier biotechnology compani...
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Senior Manager, Pharmacovigilance Quality Assurance (PVQA)

Astellas Pharma US, Inc. Northbrook
Description Astellas is the bright spot in the pharmaceutical industry -- not just because of what we do, but in the way we do it. If you are looking for a company where you can change a life, make a dream come true, and light the way for a better tomo...
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Map of Northbrook
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Director, Quality and Technological Innovation

Astellas Pharma US, Inc. Northbrook
Description Astellas is the bright spot in the pharmaceutical industry - not just because of what we do, but in the way we do it. If you are looking for a company where you can change a life, make a dream come true, and light the way for a better tomor...
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Map of Northbrook
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Assistant General Counsel - Regulatory

Astellas Pharma US, Inc. Northbrook
Description Astellas is the bright spot in the pharmaceutical industry -- not just because of what we do, but in the way we do it. If you are looking for a company where you can change a life, make a dream come true, and light the way for a better tomo...
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Map of Northbrook
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Validation Engineer II

Teva Pharmaceuticals USA Inc. Irvine
Overview Receives assignments in the form of objectives with goals and broad direction towards obtaining them pertaining to validation/qualifications of equipment and processes supporting a parenteral manufacturing facility. Responsibiliti...
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Map of Irvine
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Associate Director, Quality Assurance; Site Quality Lead

Teva Pharmaceuticals USA Inc. Mexico
Responsibilities Position Summary: This position is the Quality Site Lead for an API site and serves as a member of the Site Leadership Team. The Quality Site Lead directs the operations of Quality Control and Quality Assurance departments as a work...
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Quality Analyst I

Teva Pharmaceuticals USA Inc. West Chester
Overview Teva Biopharmaceuticals USA is committed to discovering, developing and manufacturing protein therapeutics through proprietary albumin fusion and antibody technology. Teva Biopharmaceuticals USA is a member of TEVA Pharmaceuticals Industries, ...
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Quality Analyst II

Teva Pharmaceuticals USA Inc. West Chester
Overview Teva Biopharmaceuticals USA is committed to discovering, developing and manufacturing protein therapeutics through proprietary albumin fusion and antibody technology. Teva Biopharmaceuticals USA is a member of TEVA Pharmaceuticals Industries, ...
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Map of West Chester
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Quality Analyst II

Teva Pharmaceuticals USA Inc. West Chester
Overview Teva Biopharmaceuticals USA is committed to discovering, developing and manufacturing protein therapeutics through proprietary albumin fusion and antibody technology. Teva Biopharmaceuticals USA is a member of TEVA Pharmaceuticals Industries, ...
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Map of West Chester
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Sr. Project Manager, Quality

Teva Pharmaceuticals USA Inc. Horsham
Responsibilities Key Responsibilities and Accountabilities Manage the roll out and/or the design, implementation and monitoring of  systems/processes for : 1-Process Standardization & Control Docs Mgt -Develop process for opera...
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Associate Auditor II

Teva Pharmaceuticals USA Inc. Cincinnati
Position Summary /Objective: Responsible for reviewing documentation for batches that are manufactured and packaged.   Assure compliance with cGMP before being released for further processing, packaging or commercial market. SHIFT : Mon-Th...
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Map of Cincinnati
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Sr. Quality Assurance Engineer

Teva Pharmaceuticals USA Inc. Sunrise
Responsibilitie Summary: Under general supervision, generates Annual Product Review Reports, leads investigations into product complaints and writes final complaint investigation reports.  Monitors and trends key areas and indicators from produ...
Source: CareersInPharmaceutical.com Updated 1 day 7 hours ago - show options
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Manager, Compliance (GCP)

Gilead Foster City
Specific Responsibilities Reporting to the Director of Compliance and based out of the Foster City office you will be responsible for leading the pharmacovigilance audit program, including internal process audits and external vendor audits and you will...
Source: CareersInPharmaceutical.com Updated 3 days 6 hours ago - show options
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QA Manager, Commercial API

Gilead Foster City
Specific Responsibilities With the commitment and drive you bring to the Pharmaceutical Development & Manufacturing (PDM) workplace, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfillin...
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