Sr Materials Planner
Reporting to the Materials Management Lead, the Materials Planner will provide on-going day-to-day operations and planning support to the clinical and commercial GMP Manufacturing Operations, for all products and therapeutic areas at Spark.
Responsibilities include but are not limited to:
• Lead site materials plan cycle (Raw Materials/Consumables through to Bulk Drug Substance) for GMP manufacturing
• Lead the MRP process including inventory projection and control, coordinate all aspects of supply planning and notify stakeholders of GMP manufacturing and purchasing needs
• Coordinate, review, prioritize and schedule the delivery of GMP raw materials & consumables to meet target dates and prevent stock shortage to meet the needs of manufacturing operational plans and projections
• Collaborate with partner departments to ensure material availability in alignment with manufacturing schedule, i.e.…
Medical Director of Clinical R&D – Hematology
Luitpold Pharmaceuticals, Inc., a Daiichi Sankyo Group Company, is dedicated to the development and marketing of innovative, quality drugs and medical devices for healthcare professionals, clinics, and hospitals across the United States and Canada. We specialize in sterile injectables, bone regeneration materials for dental procedures, as well as innovative products for acute pain control and veterinary medicine use.…
Scientist I – Infectious Disease Research
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.…
Scientist III, BioProcess R&D – Process Development
Job Description
When you join us at Thermo Fisher Scientific, you’ll be part of a smart, driven team that shares your passion for exploration and discovery. With revenues of $17 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.…
Head of Regulatory Strategic Medical Writing
This position is responsible for developing and implementing a vision for and leading the Regulatory Strategic Writing (RSW) team within Regulatory Affairs. In partnership with the Global Regulatory Product Team (GRPT), the RSW team drives the compilation and preparation of global critical strategic regulatory submission documents comprised of high quality, scientific justification, and relevant regulatory style/reference for submission to global health authorities to support product priorities. …
Associate Clinical Development Medical Director
The Associate Clinical Development Medical Director (Assoc. CDMD) is responsible for the scientific and medical strategy of assigned clinical trial(s), medical and scientific monitoring, and reporting of quality data. May be responsible for the scientific and medical strategy of assigned sections of a clinical development program, depending on the size and complexity. …
Senior Director, R&D
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.…
Medical Lab Scientist
At UCHealth, we do things differently
We believe in something different: a focus on the individuality of every person. In big ways and small, we exist to improve the extraordinary lives of all those we serve. As Colorado’s largest and most innovative health care system, we as a team deliver on the commitment to provide the best possible experience for our patients and their families.…
Blow Fill Seal (BFS) Pharmaceutical Manufacturing Technician
The Pharmaceutical Manufacturing Technician, Blow Fill Seal will be responsible for the set up, operation and cleaning of all pharmaceutical manufacturing/packaging equipment including; Rommelag Blow Fill Seal machine, sterilizer and labeling equipment. Personnel in this position will operate manufacturing processing equipment by following standard operating procedures and batch records in accordance with FDA current Good Manufacturing Practices.…
Global Lead, Clinical Trial Disclosure and Transparency Lead
The Global Lead, Clinical Trial Disclosure and Transparency is a key leadership position responsible for providing strategic leadership, development, and management of CSLs global Clinical Trial Disclosure and Transparency function. The incumbent will lead and develop the group responsible for clinical trials registration, summary results disclosure, data disclosure and transparency responsibilities in all regions across the global CSL organization according to CSL policy. …
Senior Scientist – Sterile Liquid Commercialization
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its 125-year legacy.…
Assay Development Associate – Vector Shedding/Bio Distribution
The Assay Development Associate – Vector Shedding/Bio Distribution will:
•With guidance and supervision from the group leader or supervisor, conduct clinical and preclinical sample analysis per SOPs and generate data with high scientific quality to meet GLP regulatory expectations.
•Participate in validation of bioanalytical assays such as immunoassays and cell-based assays. …
Manager of Quality Assurance Validation
Summary
The role of the QA Validation Manager is to ensure compliance with company and regulatory requirements e.g. Good Manufacturing Practices (GMP), Code of Federal Regulations (CFR) and local regulations. The QA Validation Manager, directly reporting to the Quality Director, manages the QA Validation Specialists, coordinates and schedules all activities to assure that all new or existing pieces of equipment, utilities, instruments, analytical methods and processes are adequately qualified and validated in accordance with the requirements outlined in the approved Validation Master Plan requirements, the approved validation test protocol, applicable policies and procedures, through review of the aforementioned documentation and collaboration with the responsible party. …
QC Analytical Sciences Scientist
The primary goals of Analytical Sciences are: to lead the phase-appropriate optimization, qualification, verification and validation of analytical methods across the product development lifecycle from clinical to commercialization; provide support to QC in the investigation of non-conformances, invalid assays; and troubleshooting method problems.…
LIMS/PIMS Administrator
JOB SUMMARY
The Laboratory Information Management System (LIMS) / Pretreatment Information Management System (PIMS) Administrator is responsible for the effective provisioning, installation, configuration, operation, and maintenance of systems hardware and software and related infrastructure. Ensures that system hardware, operating systems, software systems, and related procedures adhere to organizational policies and processes, enabling staff to achieve departmental objectives effectively and efficiently.…
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.…
Manufacturing Validation Engineer
GE is the world's Digital Industrial Company, transforming industry with software-defined machines and solutions that are connected, responsive and predictive. Through our people, leadership development, services, technology and scale, GE delivers better outcomes for global customers by speaking the language of industry. …
In-Vivo Research Associate I
About Us:
Vium empowers biomedical investigators with technology that accelerates the preclinical drug discovery and development pipeline. Researchers can design, run, and analyze experiments that rapidly surface insights and high volumes of quality data. The platform improves the speed and reproducibility of preclinical research so that it is more predictive of how drugs perform in humans.…
Senior R&D Project Manager
Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model – Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceuticals and biologic products for patients around the world.
Allergan markets a portfolio of best-in-class products that provide novel treatments for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology, anti-infective and cardiovascular therapeutic categories.…
Global Coordinator, Pharmacovigilance job
GE is the world's Digital Industrial Company, transforming industry with software-defined machines and solutions that are connected, responsive and predictive. Through our people, leadership development, services, technology and scale, GE delivers better outcomes for global customers by speaking the language of industry. …
