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- Boston, MA
new job!

As a senior applied scientist, you will invent, build and deploy state of the art machine-learning models and systems to enable and enhance the team's mission. You will develop a long-term scientific agenda, initiate and lead scientific projects and mentor applied scientists. You will present your work to product and engineering teams, publish scientific papers and apply for patents for your inventions. You come with experience defining research vision and getting buy-in from senior research....


My client has a great opportunity to make an impact in the Neuropharmacology field. They are looking for a Scientist in the Behavioral Pharmacology group to take on the following tasks:Design and perform experiments (with a focus on traumatic brain and spinal cord injuries and PTSD)Effectively document results, perform data analysis, and write reports.Conduct surgeries, handling, dosing (IV, SC, IP, and PO), pharmacology, tissue dissections and testing.Write grants to support trauma research....


My established client seeks a Scientist in the Neurodegeneration group to take on the following tasks:Perform experiments using behavior assays assessing motor and cognitive dysfunctionDemonstrate strong leadership skills and train/supervise scientists as neededManage data and perform statistical analysisPrepare and deliver presentations and reports, and contribute to manuscript preparationThe ideal candidate will possess the following qualities:Ph.D. degree in Neuroscience or similar....

- New York, NY

Head of Gene Therapy CMC My client is expanding and looking to bring on a new person to lead CMC for Gene Therapy. The ideal candidate will take on the following tasks:Plan, lead and communicate the CMC related strategies for gene therapy products, including selecting CROs and CMOs.Actively manage CRO/CMOs for process optimization, scalable cGMP manufacture (both Drug Substance and Product) to supply a multi-product portfolio of pre-clinical and clinical gene therapy development....

- Menlo Park, CA

Education and Qualifications - M.D. ; Specialization in Hematology/Blood Cancers. - Preferable five to seven years clinical or clinical development experience in the biotechnology or pharmaceutical industry or a combination of academia and industry. - Expertise in Phase I clinical oncology studies. Overview The Medical Director will collaborate with company management, design, plan and develop clinical evaluation research studies in hematology oncology. He / She will prepare, author and....

- Pittsburgh, PA

Our client is recognized around the world as an innovative leader in the development, manufacturing, and commercialization of science-based nutritional health products. Their company is headquartered in Montreal, Canada and we have offices and manufacturing plants around the globe. We are currently hiring for a Scientist (Technical Services) in Pittsburgh, PA. General FunctionIdentify and resolve manufacturing issues for commercial and development products. Use good technical judgment to make....

- Charlotte, NC

We are looking for a Validation Manager who is an experienced people manager, with technical knowledge of pharmaceutical aseptic filling operations and equipment and solid dosage operations and equipment. In addition, the candidate will be responsible for leadership of highly complex compliance projects and initiatives such as New Product Introduction and Cleaning Validation Program. These projects require close collaboration Quality as well as other departments. This individual will also....

- Harrisburg, PA

WHY YOU MIGHT BE INTERESTED This position will lead all site quality in QA and QC. This company is a well know on the world stage and is growing everyday. You will have 4 direct reports and about 30 indirect. WHAT WILL YOU DO IN THIS ROLEWorking with the global requirements to keep the Quality Management System in line with the local team. Department budgeting, personnel, investment planning for long-term objectivesWill work on all ISO Certifications in regards to cGMP compliance and auditsSet


We are looking for a Senior Regulatory Affairs Manager who will play a primary and integral role in the regulatory activities and initiatives at the facility. Incumbent will guide US regulatory strategies across multiple programs at this emerging facility, lead pre and post-approval submission activities, and serve as regulatory lead to interdisciplinary cross-functional groups across entire product life cycles. Key Responsibilities:Coordinate ANDA submissions to FDA, interact with regulatory....

- Lancaster, SC

We are looking for a qualified individual who has the understanding and knowledge of development of chromatographic, spectroscopic, titrimetric and wet chemistry methods. Implements strategies to ensure effective achievement of scientific objectives. Monitors and evaluates completion of tasks and projects.Roles and Responsibilities:Has hands on knowledge and can begin the development and validation of scientifically sound analytical methods for Product release and stability testing.Familiarity


Lead Controls Validation Engineer - Mechatronic Systems Farmington,MI Summary of the Lead Controls Validation Engineer - Mechatronic Systems Job : The Lead Controls Validation Engineer will play a key role in the development of leading edge automotive technology for mechatronics. If you are interested in bleeding edge technology such as: Stability Control, Electronic Braking, Driverless Cars, Automated Driving, ADAS and Collision Avoidance this is were you should be. You will be responsible....


Lead Electronic Test Engineer - Mechatronic Systems Farmington,MI Summary of the Lead Electronic Test Engineer - Mechatronic Systems Job : A Mechatronics Systems Test Engineer is required to play a key role in the development of the latest automotive technology in electromechanical systems. If you are interested in bleeding edge technology such as: Automated Driving, Stability Control, Electronic Braking, Driverless Cars, Collision avoidance this may be were you should be. You will be....


Director of Clinical Development Cardio This global Pharmaceutical company is the worldwide biologics research and development leader. 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. As a Director, Clinical Development in Gaithersburg MD or Cambridge UK, you’ll play a pivotal role in....


We are looking for a Quality Assurance Validation Technician who will provide Quality Assurance support for validation activities associated with equipment, processes, facilities, and computer software/systems to ensure compliance with applicable current Good Manufacturing Practice (GMP) regulations, corporate policies, and site Standard Operating Procedures (SOP). Work closely with the various departments in the design and development of validation protocols to ensure the purpose, testing and


Require a highly motivated and experienced individual for the position of Sr. QA Associate II. This individual will be part of the External Commercial QA group. Responsibilities include supporting Supplier Quality Management activities. Performs vendor audits, supports changes, complaints and queries related to external vendors. Troubleshoots issues, develops and implements effective risk mitigation strategies as required. Collaborates with site operations to insure site expectations of....


This is a new position for this company and you will be the subject matter expert in Injection Molding for them. Duties Include:Development of new processesUse of scientific molding principlesTrain and coach Injection Molding techniciansRecommend equipment to automate molding processEstablish requirements for equipment, tooling and materialsRequirements: Three plus years in Injection Molding Process Engineering with understanding in many areas such as materials, equipment, tooling, scientific....


We are looking for Technical Document Reviewer with pharma experience. This position will be responsible for working within the Quality Systems organization supporting the review, development and implementation of harmonized documents, processes and systems. General Responsibilities:Review of documentation from various suppliers and other sites for use at site.Creation of site-specific specifications, standard test procedures, general test procedures, test data sheets and any other....

- Charlotte, NC

We are looking for a Microbiology Technician who will support the Quality Control group to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the microbiology, environmental monitoring, and utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production area, and supporting quality initiatives. The individual routinely conducts monitoring, testing, SOP....


Are you a Product Design Engineer with experience designing injection molded products that contain many small parts? Are you a Product Design Engineer who has experience in the consumer products industry? Are you a Product Design Engineer who wants to play an integral role in the growth of well established publicly held company? If you can answer yes to these questions, you should consider this opportunity. As Product Design Engineer, in a very hands-on role a summary of your overall role will


Our client is a world leader in laboratory equipment and services, and has an opportunity for a Technical Sales Representative (TSR) for its industry leading analytical instrumentation used in R&D laboratories. The Technical Sales Representative will be responsible for direct sales of mechanical surface characterization instrumentation and services to customers covering OR, WA, ID, MT, CO, WY, & UT with an ideal base close to Portland or Seattle. The product lines include Atomic Force....

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