Associate Department Coordinator, Drug Product Manufacturing
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)? …
Institute Associate Scientist II – Drug Metabolism and Pharmacokinetics group
The Institute for Applied Cancer Science (IACS) is seeking a highly motivated and team oriented individual to join our drug metabolism and pharmacokinetics research group to support the Institute’s fast-paced drug discovery programs.
The Institute Associate Scientist II will provide the drug discovery team with invaluable information regarding the stability of their new drug candidates in plasma, microsome and hepatocyte stability experiments, and quantify the amount of drug candidate in biologic fluids using the latest mass spectrometry techniques using state-of-the art instrumentation.…
Laboratory Sales Specialist
Laboratory Sales Representative
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.…
QC Analyst
If you're inspired by the possibilities of science to change lives and you thrive when making brave decisions – join us.
At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality.…
Scientist AR&D
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.…
Manager, Quality Assurance
Overview
Kashiv Pharma, LLC. is an emerging pharmaceutical research and drug delivery company focused on developing innovative technologies, improved medicines and life cycle management products. Kashiv also offers contract research and development services to pharmaceutical clients in need of formulation and analytical development expertise and/or clinical supply manufacture. …
Health and Safety Engineer
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.…
Project Coordinator
Overview
A Project Coordinator is a proactive, performance-driven professional with expertise in pharmaceutical project management and planning. They must support projects from initiation through filing, approval, and launch.
Must have a keen understanding of business priorities. A results driven team player who is committed to managing projects, and keeping timelines while maintaining costs. …
Technical Writer
Overview
Prepare documentation to include specifications, method verification/validation reports, method transfer reports, and characterization reports as and when needed in appropriate format required by regulatory affairs.
Review, revise and draft Standard Operating Procedure documents.
Working efficiently to setup Active Pharmaceutical Ingredients (API) as well as Finished Product (FP) specification based on API manufacturers drug master file (DMF), United state Pharmacopeia (USP) monograph and ICH guidelines with the help of group leader and scientist. …
Sr. Scientist R&D – Analytical
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.…
QA Director
Overview
The Quality Assurance Director is responsible for maintenance of Kashiv Pharma’s quality management system, supervise QA Associates, documentation/ SOPs, change controls, deviations/ investigations, master code book, raw material & finished product final QA release (COA- Certificate of Analysis issuance), batch record review, quality assurance (QA) duties, regulatory compliance (RC), stability program, facility / equipment qualifications, equipment cleaning verifications/ validation, training and ensuring that operations are conducted in accordance with current Good Manufacturing Practices. …
Respiratory Medical Science Liaison/Sr. MSL – NY Metro
At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We're focused on the potential of science to address the unmet needs of patients around the world.…
Respiratory Medical Science Liaison/Sr. MSL – Wisconsin/Iowa
At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We're focused on the potential of science to address the unmet needs of patients around the world.…
R&D Associate II/Associate Scientist I
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.…
Recruiter
Job description
Job Title: Medical Technologist
Location: Chicago, IL
Start Date: ASAP
Major Responsibilities:
- Must Have MT or MLT (ASCP)
- Perform laboratory testing while ensuring quality patient care.
- Innovation (Process Improvement) – Suggests and develops new ideas and approaches in the workplace.
Bispecific Antibody Engineering and Development Scientist I/II – (Gaithersburg, MD)
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.…
Senior Marketing Manager
At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We're focused on the potential of science to address the unmet needs of patients around the world.…
QC Representative – Microbiology
QC Representative – Microbiology
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)? …
Oncology Medical Science Liaison/Sr. MSL (Women’s Cancer) – NC/SC/VA
At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We're focused on the potential of science to address the unmet needs of patients around the world.…
Director Clinical Safety Physician (f/m) Therapeutic Area Immunology
To provide guidance and expertise on all aspects of clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and state of the art pharmacovigilance post approval. Apply sound medical judgment for analysis and interpretation of complex clinical and postmarketing safety data for signal detection and initiation of safety risk management activities including safety specification, PV planning and risk minimization/mitigation.…
