POSTDOCTORAL ASSOCIATE , Koch Institute (KI) for Integrative Cancer Research , to lead cutting edge projects to better understand cancer immunology and develop new immunotherapies. To accomplish this, lab projects involve approaches from molecular and synthetic biology, immunology, glycobiology, and biological engineering. Experimental approaches used will include cloning

Synthesize molecules intended for Clinical Trials Materials (CTM) under cGMP guidelines in CIL's GMP facility Develop and optimize synthetic routes as necessary Create new or revise procedures and batch records as needed Participate in inter departmental meetings Participate in the preparation of project outlines for new projects Maintain the labs with the required equipm

Under general supervision, assist in the performance of laboratory research and procedures by performing a variety of routine experimental techniques such as electrophoresis, centrifugation, chromatography, and the like. Collect, verify, record, and compile data and information in support of research. Essential Duties and Responsibilities (Specific duties will depend on n

Primary Work Address 1 Baylor Plaza, Room S101, Houston, TX, 77030 Current HHMI Employees, click here to apply via your Workday account. We are always open to finding self motivated and highly organized Lab Manager candidates for potential opportunities within our labs in Texas. Applications are accepted on a rolling basis. You will be contacted by a member of our Recruitm

Do you want to join a team where the mission is meaningful, the challenges are complex, and you can directly see the results of your hard work? At Lundbeck, we are tirelessly dedicated to restoring brain health, so every person can be their best. Inspired and driven by our purpose, we are the only global biopharmaceutical company focused solely on brain diseases. We have

Laboratory Tech I or II Third Shift Job Locations US RI Providence ID 2024 5987 Category Clinical Laboratory Type Regular Full Time Overview In 1979, the Rhode Island Blood Center was established by the hospitals in Rhode Island as a private, not for profit agency to collect, test, and distribute blood products. Today, the Rhode Blood Center is a division of New York Bloo

The Faden Lab is seeking a highly motivated post doc to join our team of scientists and clinicians working at the forefront of cancer biomarkers and diagnostics. We design liquid biopsies to non invasively screen, diagnose, and monitor head and neck cancers and utilize these custom assays to answer translational and clinical questions that advance patient care. Our lab is

Collects and organizes patient data Maintains records and databases Uses software programs to generate graphs and reports Assists with recruiting patients for clinical trials Obtains patient study data from medical records, physicians, etc. Conducts literature searches Verifies accuracy of study forms Updates study forms per protocol Documents patient visits and procedure

The Post Doctoral Fellow will become proficient in the following duties (examples, but not limited to) routine molecular biology (PCR, recombinant DNA cloning, bacterial transformations, etc.), biochemical techniques, mammalian cell culture, assessment of genome editing technologies in bacteria and mammalian cells, DNA sequencing methods (Sanger, Illumina next generation

The Opportunity Avantor is looking for a detail centric Quality Assurance Specialist I to join our Quality Assurance Specialist team. Our Quality Assurance Specialist Team upholds and maintains Avantor's operational continuity, including documentation ownership by maintaining quality and industry standards, meeting production deadlines, and closely working with associates

Lead a team of software engineers in designing, developing, and testing software for medical devices, ensuring compliance with industry standards and regulations. Assess and revise development process and procedures. Drive to a fuller implementation of the Agile methodology, improved productivity and higher quality Measure developer/team velocity per sprint, giving guidan

Manage day to day efforts and coordinate calendar of assigned team to ensure adequate pre and post sales support for designated products. Assist in setting of priorities where needed, based on business drivers. Learn the MACSima training process and support process to ensure the success of select priority customers with installation training and follow up support Work wit

The Quality Control Analyst I performs assays to ensure product quality standards are met, participates in process and product development, troubleshooting activities, and initiates and implements programs focused on stability testing. RESPONSIBILITIES (include but are not limited to) Job performance will involve a variety of activities including Independently compile, an

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovativ

Serves as the Regulatory Affairs lead on cross functional MDR project teams Ensures compliance with EU Medical Device Regulations (MDR) and EU guidance throughout the project. Actively participates in EU MDR project teams by attending meetings, collaborating with the project manager and cross functional team members, and communicating regulatory requirements and guidance