SPEC – QUALITY ASSURANCE Job
Description
PurposeThe Specialist, Quality Audits and Relationship Management, is responsible for maintaining, establishing and improving Novo Nordisk Inc.’s (NNI) end-to-end Quality audit program. In the role of Quality Lead Auditor, the position is responsible for all aspects of Quality auditing, including Quality audit planning, execution, reporting and follow-up to ensure compliance with all applicable GxP regulations, and Novo Nordisk policies and procedures.…
Snr Dir Early Clinical & Translational Medicine
The Senior Director, Early Clinical & Translational Medicine is a highly strategic and influential senior medical leadership role within R&D. The position within the Clinical Pharmacology & Early Development (CPED) function, is focused on both providing and leading crucial clinical and translational medicine input to early stage R&D projects (typically from mid-stage Research up to clinical proof-of-concept).…
Director, Global Regulatory Affairs, Early Development Therapeutic Area Lead, Development Products
Accountable to provide innovative, tactical and strategic regulatory leadership regarding maximizing the alignment between global regulatory strategies for development of drugs/new indications and regional regulatory strategies for the assigned development projects of the TA.
Provides global regulatory oversight for assigned therapeutic area(s), focused on pre-clinical and clinical aspects of drug development and associated regulations. …
Manufacturing Associate – Process Development Rotation
Overview
People are at the center of who we are and what we do.
Are you seeking…
– A culture defined with the help of your voice?
– Recognition for your talent and continued growth opportunity?
– Upfront tuition assistance (eligible day one of employment)? …
Senior Manager, Quality Assurance & Regulatory Strategic Initiatives
Serves as the Quality lead for all strategic expansion projects. Responsible for assuring project activities are in agreement with Kankakee site, CSL Behring and industry standards regarding Quality Assurance, Validation, Change Management and Compliance requirements. Assures appropriate documentation is provided to support project activities including product license requirements.…
Senior Clinical Pharmacometrician, Early Clinical Development
AstraZeneca is dedicated to discovering, developing, and delivering innovative, meaningful medicines and other healthcare solutions that help enrich the life of patients, as well as their families and communities. At AstraZeneca Oncology, our vision is redefining cancer, redefining our solutions to cancer and restoring patients' lives.…
Scientist I/II – Analytical
If you're inspired by the possibilities of science to change lives and you thrive when making brave decisions – join us.
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.…
Clinical Research Associate Field Management Charlotte North Carolina Job
Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and Standard Operating Procedure (SOPs). Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within Clinical Medical Regulatory (CMR).…
Scientist – Pre-Formulation
Overview
Located in Bridgewater, New Jersey, Kashiv Pharma is an emerging pharmaceutical research and drug delivery company focused on developing innovative technology platforms and novel drugs with clinical differentiation and a compelling value proposition for patients, physicians, and payers. We have developed a portfolio of proprietary drug delivery technologies to improve the efficacy, safety, compliance, and dosage of low bioavailability drugs where absorption could be limited due to solubility, permeability, and stability problems.…
Pharmacovigilance Scientist
Pharmacovigilance Scientist #job in Gaithersburg, MD – AstraZeneca Pharmaceuticals
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.…
Labware LIMS condultant
Role : Labware LIMS
Location: Cambridge MA
Duration: Contract
JD for LIMS Enhancement
- Experience in Labware LIMS V6 and above
- Experience in executing enhancements and user defined customizations using LIMS Basic.
- Experience on master data builds in Labware LIMS application and on instrument interfaces
- Support different modules of LIMS like Lot manager, Environmental monitoring & Water, Stability Manager, Reporting, Standard & Reagents, Instrument Manager, Label Printing.
Pharmacovigilance Scientist
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 continuously forge partnerships that help pursue world-class medicines in new ways, combining our people's exceptional skills with those of people from all over the globe.…
Labware LIMS
Hi,
Hope you are all doing great..
Position : Labware LIMS
Location : Cambridge , MA
Duration : Contract
JD for LIMS Enhancement
- Experience in Labware LIMS V6 and above
- Experience in executing enhancements and user defined customizations using LIMS Basic.
Principal Clinical Scientist
The Principal Clinical Scientist will work closely with the Senior Global Clinical Program Director and Director Clinical Development Scientist to drive the clinical development program as dictated by therapeutic area/ project needs. The position holder is responsible for both scientific input to clinical development strategies, acting as the primary liaison between the assigned therapeutic area and key stakeholders to ensure translation of the development plan into operational deliverables.…
Labware LIMS Consultant
Role : Labware LIMS
Location: Cambridge MA
Duration: Contract
JD for LIMS Enhancement
- Experience in Labware LIMS V6 and above
- Experience in executing enhancements and user defined customizations using LIMS Basic.
- Experience on master data builds in Labware LIMS application and on instrument interfaces
- Support different modules of LIMS like Lot manager, Environmental monitoring & Water, Stability Manager, Reporting, Standard & Reagents, Instrument Manager, Label Printing.
Head of Oncology IMED Strategy
The Head of Oncology IMED Strategy is a key member of the MedImmune Oncology IMED leadership team which is responsible for the research and early-stage development activities of the oncology biologics pipeline within AstraZeneca. The Head of Oncology IMED Strategy will provide strategic leadership, counsel, and support to the SVP of the Oncology IMED and other leaders within the oncology therapeutic area at MedImmune.…
Director, Quality
Leading research and manufacturing organization serving the pharmaceutical and biotechnology industries seeks senior level Quality Manager to direct Quality Assurance and Quality Control function. The Director, Quality ensures company implementation and adherence to regulatory and quality policies and standards, as well as, drives quality improvement activities based on industry best practices while maintaining a company quality culture.…
Scientist I – Microbial Sciences
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 companies, our mission is centered on delivering life-changing products that advance world health, and help fight and cure disease. …
Sales Consultant-Laboratory
Sales Consultant-Laboratory
Working at METTLER TOLEDO means you are impacting the world in important ways. Our precision measuring devices span the world's laboratories, production facilities, and retail stores. We manufacture, sell, and service instruments that detect, measure, and weigh – from the infinitely small to the largest of vehicles or airplanes.…
Clinical Program Manager
The Clinical Program Manager (CPM) is accountable for the on-time delivery of a clinical program for an assigned Therapeutic Area.
The CPM is responsible for clinical operational planning activities and is accountable for leading program/study execution. The CPM leads one or more studies and may take on additional responsibilities as dictated by project size and complexity with minimal oversight.…
