The primary responsibilities of this role, Associate Director, Analytical Development , are to Acts as a visionary, architect, coach, and catalyst (VACC) to teams thus driving NPD and transformational science projects; Lead analytical development (AD) activities of differing complexities associated with new product development (NPD) for global markets. The activities incl

Primary responsibility is preparation of validation protocols (IQ/OQ) and commissioning documents for equipment and control systems. Work with control system programmers to develop and execute factory acceptance software test documents. Work as an integral member of a project team. Interface with the equipment manufacturing companies and internal departments to obtain the

Develops qualification protocols, and associated reports while adhering to a change management process. Supports the execution of equipment qualifications and validation protocols. Supervises vendors for qualification functions. Develops written procedures for calibration and preventive maintenance of equipment. Supports equipment qualification and validation activities.

To perform a variety of nuclear medicine exams for the diagnosis of pathological conditions. EDUCATION Completion of an accredited Nuclear Medicine Program and valid license from the State of New Jersey DEP. Certification in The American Registry of Radiologic Technologists (ARRT) or Nuclear Medicine Technology Certification Board (NMTCB). Current CPR cer EXPERIENCE No pr

Job Title Associate Scientist II Job Id 24 01899 Location East Hanover, NJ Duration 05 Months On W2 Contract The role is to provide technical lab support to project managers. Familiarity with sample prep, bench based chemistry and measurement techniques, data collection and data management. Experience working in a lab environment is a must. We are looking for a candidate

You ensure optimal patient outcomes related to chronic and specialty drug related disease states. Your tasks include preventing or resolving medication related issues and optimizing drug therapy. You serve as a resource and drug expert to patients, families, physicians, nurses, and other healthcare professionals. Additionally, you play an integral role in educating pharma

Design, execute, oversee, and interpret experiments in partnership with other team members. Independently draft, review, and finalize both technical protocols and scientific reports while interacting in a cross specialty environment. Help determine process parameters range for cell culture and downstream processing to optimize PSC starting material yield and quality in a

Prepare samples for analytical and microbiological testing of food products, ingredients, and environmentals. The role is responsible for the application of approved microbiological techniques and methodologies used in analytical testing. ESSENTIAL RESPONSIBILITIES Prepare samples for indicator organisms, pathogens, and chemistries Apply aseptic techniques in daily worklo

Tris Pharma, Inc. (www.trispharma.com) is a leading privately owned biopharmaceutical company in the U.S. with a focus on development and commercialization of innovative medicines that address unmet patient needs. We have more than 150 US and International patents including applications and have marketed several branded and generic products in the U.S., have licensed our

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 Dept of Molecular Biology, Princeton, NJ, 08544 Current HHMI Employees, click here to apply via your Workday account. About the Lab We currently have an opening for a Research Technician to join the laboratory Dr. Cliff Brangwynne at Princeton University. The Brangwynne lab works on understanding phase transitions in living cells, including the develop

Company Description Join us and make YOUR mark on the World! Are you interested in joining some of the brightest talent in the world to strengthen the United States' security? Come join Lawrence Livermore National Laboratory (LLNL) where our employees apply their expertise to create solutions for BIG ideas that make our world a better place. We are committed to a diverse a

G reeting patients upon arrival to the clinic Explaining the benefits of our specialty pharmacy and successfully enrolling patients into the program Performing all insurance benefit investigations, prior authorization, claim rejects, overrides, etc. Working with patients to find financial aid (grants, manufacture programs, discount cards, etc.) to ensure they have access

The Clinical Trial Assistant (CTA) will be responsible for a wide variety of matters in support of Pharming's growth as we increase the number of both pipeline and marketed products. Core functions include Set up, organize, and maintain clinical study documentation (e.g. Trial Master File documents, clinical study site documents, email correspondence, training materials,

Oyster Point Pharma, Inc (Delaware corp) At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via Access Providing high quality trusted medicines regardless of ge