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Associate Director- Ethics and Compliance Business Partner Job

Novo Nordisk Inc. - Plainsboro, NJ

Business Manager, Claims, Compliance, Diabetes, Field Sales, Finance, Healthcare, Insurance, Law, Legal, MBA, Management, Manager, Medical, Pharmaceutical, Pharmaceutical Sales, Project Manager, Risk Management, Sales, Science, Special Medicine, Technology

From Novo Nordisk Inc.- 11/22/2017 5:41:02 AM

Director - Clinical Development & Medical Affairs - Hemostasis Job

Novo Nordisk Inc. - Plainsboro, NJ

Clinic, Clinical Research, Compliance, Diabetes, Healthcare, Hematology, ICU, Law, Legal, Management, Manager, Medical, Medical Research, Medical Technologist, Pharmaceutical, Pharmaceutical Sales, Regulatory Affairs, Research, Research Scientist, Sales, Science, Special Medicine, Travel Nurse

From Novo Nordisk Inc.- 11/22/2017 5:41:02 AM

Manager, Metrology Job

Novo Nordisk Inc. - Clayton, NC

Business Process, Diabetes, ERP, Engineer, Engineering, Facilities, Healthcare, Instrumentation, Law, Legal, Management, Manager, Medical, Operations, Pharmaceutical, SAP, Science, Special Medicine, Technology

From Novo Nordisk Inc.- 11/22/2017 5:41:02 AM

QC Microbiologist Job

Novo Nordisk Inc. - West Lebanon, NH

Compliance, Diabetes, Electrical, Engineering, Facilities, Healthcare, Housekeeping, Laboratory, Legal, Medical, Microbiology, Operations, Science, Special Medicine

From Novo Nordisk Inc.- 11/22/2017 5:41:02 AM

QC Analyst - Analytical Job

Novo Nordisk Inc. - West Lebanon, NH

Analytics, Compliance, Diabetes, Electrical, Engineering, Healthcare, Laboratory, Legal, Management, Medical, Science, Special Medicine

From Novo Nordisk Inc.- 11/22/2017 5:41:02 AM

Sr. Counsel, Commercial, North America

CSL Behring - King of Prussia, PA

Education:  Bachelors Degree and a Juris Doctor.  Superior academic credentials at top-tier law school strongly preferred.     Experience: Must be licensed to practice law in Pennsylvania (preferred), or hold (or be eligible for and able to obtain promptly) a Limited In-House Corporate Counsel License under PA BLE Rule 302.  Minimum of 7 years applicable Legal and/or Compliance experience requir ...more

From CSL Behring- 11/22/2017 5:40:35 AM

Scientist I - Clinical Immunology & Bioanalysis

MedImmune - South San Francisco, CA

Requirements/Qualifications: Education : Ph.D or advanced degree in Biological Sciences or related field   Experience : •1-5 years of post-doctoral experience in immunology, oncology or cell biology •Expertise in cell-based biomarker assay development using human biological specimens •Experience with BD flow cytometry platforms (e.g. FACSCantoII, LSRII, FACSAria) •Experience with cell sorti ...more

From MedImmune- 11/22/2017 5:40:21 AM

Senior Analyst, QCIS - (Frederick, MD)

MedImmune - Frederick, MD

Main Duties and Responsibilities Scope •You will perform day-to-day activities of QC computerized systems, such as LIMS, OpenLab, Empower, and lab computer systems •You will perform application administration tasks for QC computerized systems •You will be a liaison between QC and the Validation group with relation to software/computer system validation •You will be a liaison between QC and ...more

From MedImmune- 11/22/2017 5:40:21 AM

Associate Scientist I - Microbial Sciences

MedImmune - Gaithersburg, MD

Requirements/ Qualifications: Associate Scientist I: BS in biological sciences plus 5-8 years relevant laboratory experience in industry or MS in biological sciences plus 3-6 years relevant laboratory experience in industry Specific skills: Broad experience required in murine bacterial infection modeling, microbiologic laboratory skills (strain isolation and subculture) immunologic assays (flow c ...more

From MedImmune- 11/22/2017 5:40:21 AM

Associate Director, QA Validation - (Frederick, MD)

MedImmune - Frederick, MD

Main Duties and Responsibilities As an Associate Director, QA Validation, you will be responsible for all assigned aspects of Quality Assurance at the Frederick Manufacturing Center associated with: •Owning the Validation program and strategy •Quality oversight for the execution of Facility, Utility and Equipment system •Quality oversight for the execution of Automation qualification and val ...more

From MedImmune- 11/22/2017 5:40:21 AM

Senior Director, Immuno-Oncology

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Main Duties and Responsibilities The Senior Director, Immuno-Oncology will manage large global or regional studies within the Immuno-Oncology franchise and will be involved in the design, conduct, monitoring, data interpretation and reporting of individual clinical trials, ensuring that all clinical studies operate to the highest ethical and safety standards and in compliance with Good Clinical P ...more

From AstraZeneca Pharmaceuticals- 11/22/2017 5:40:11 AM

Study Physician - Immuno-Oncology

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Main Duties and Responsibilities The Study Physician will manage global or regional studies within the Immuno-Oncology franchise and will be involved in the design, conduct, monitoring, data interpretation and reporting of individual clinical trials, ensuring that all clinical studies operate to the highest ethical and safety standards and in compliance with Good Clinical Practice (GCP) and regul ...more

From AstraZeneca Pharmaceuticals- 11/22/2017 5:40:11 AM

Project Coordinator, PMO – Global Biologics Operations - (Gaithersburg, MD)

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Main Duties and Responsibilities As the Project Coordinator, PMO - Biologics Operations, you will support Global Biologics Operations' projects, project execution processes, project reporting, and portfolio within the Program Management Office (PMO).  Interfaces with project sponsors, project managers and core team members for meetings, action updates, minutes.  Supports the project managers with ...more

From AstraZeneca Pharmaceuticals- 11/22/2017 5:40:11 AM

Scientist I - Clinical Immunology & Bioanalysis

AstraZeneca Pharmaceuticals - South San Francisco, CA

Requirements/Qualifications: Education : Ph.D or advanced degree in Biological Sciences or related field   Experience : •1-5 years of post-doctoral experience in immunology, oncology or cell biology •Expertise in cell-based biomarker assay development using human biological specimens •Experience with BD flow cytometry platforms (e.g. FACSCantoII, LSRII, FACSAria) •Experience with cell sorti ...more

From AstraZeneca Pharmaceuticals- 11/22/2017 5:40:11 AM

Senior Analyst, QCIS - (Frederick, MD)

AstraZeneca Pharmaceuticals - Frederick, MD

Main Duties and Responsibilities Scope •You will perform day-to-day activities of QC computerized systems, such as LIMS, OpenLab, Empower, and lab computer systems •You will perform application administration tasks for QC computerized systems •You will be a liaison between QC and the Validation group with relation to software/computer system validation •You will be a liaison between QC and ...more

From AstraZeneca Pharmaceuticals- 11/22/2017 5:40:11 AM

Associate Scientist I - Microbial Sciences

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Requirements/ Qualifications: Associate Scientist I: BS in biological sciences plus 5-8 years relevant laboratory experience in industry or MS in biological sciences plus 3-6 years relevant laboratory experience in industry Specific skills: Broad experience required in murine bacterial infection modeling, microbiologic laboratory skills (strain isolation and subculture) immunologic assays (flow c ...more

From AstraZeneca Pharmaceuticals- 11/22/2017 5:40:11 AM

Diabetes Sales Specialist – Cleveland E, OH

AstraZeneca Pharmaceuticals - Cleveland, OH

Main Duties and Responsibilities: You will develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients.  You will demonstrate a deep, clear and thorough understanding of the Diabetes disease st ...more

From AstraZeneca Pharmaceuticals- 11/22/2017 5:40:11 AM

Associate Director, QA Validation - (Frederick, MD)

AstraZeneca Pharmaceuticals - Frederick, MD

Main Duties and Responsibilities As an Associate Director, QA Validation, you will be responsible for all assigned aspects of Quality Assurance at the Frederick Manufacturing Center associated with: •Owning the Validation program and strategy •Quality oversight for the execution of Facility, Utility and Equipment system •Quality oversight for the execution of Automation qualification and val ...more

From AstraZeneca Pharmaceuticals- 11/22/2017 5:40:10 AM

Incoming Quality Control Technician

AstraZeneca Pharmaceuticals - West Chester, OH

Main Duties and Responsibilities As Incoming Quality Control Technician, you will autonomously perform tasks related to inspection and sampling to support the release of production materials and components.  Perform testing of samples. Maintain and troubleshoot testing equipment. •Prepare documentation of activities, actions, and results. Ensure proper documentation practices during job activi ...more

From AstraZeneca Pharmaceuticals- 11/22/2017 5:40:10 AM

Gold Associate (P)

Catalent Pharma Solutions - Somerset, NJ

Job Description The Global Operations Leadership Development (GOLD) program is an intensive, two-year leadership development opportunity consisting of three separate rotations, each lasting eight months in duration, at different Catalent sites in the United States.   It is designed for university graduates who have a strong desire to accelerate their career growth in an entrepreneurial, fast-pace ...more

From Catalent Pharma Solutions- 11/22/2017 5:39:40 AM
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