Lab Supervisor Clifton, NJ Monday to Friday 8 00AM 5 00PM Under direction of the manager/director, plan, organize, schedule and direct the work of the section in order to effectively maximize employees, equipment and material utilization within budgetary constraints while adhering to quality technical standards. Accountable for quantity and quality of specimens handled an

The Scientist I, Chemistry contributes to PTC's drug discovery efforts by synthesizing small molecules in support of internal lead optimization programs. The incumbent is responsible for independently planning and executing synthetic organic chemistry protocols to efficiently obtain desired targets for biological assays. The selected candidate is also responsible for inte

The Associate Director, Reimbursement and Access (RAD) 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 Handling all coverage, reimbursement and access needs across their territories/regions and work directly with their respective RAM's, Ruconest Patie

Perform Mechanical measurements and visual quality assessments of received items, work in progress and finished goods Performs 1 st Piece Inspection on machined parts and inspection for product Quality Analysis. Inspect with thread gages, GO/NO GO plug gages, V Blocks, Gage Blocks, height stands, dial indicators, various types of ID/OD micrometers, inspection of thread Pi

The Senior Clinical Research Liaison will function as the Lead in the development, monitoring, and completion of clinical registries. This position will be the primary contact with healthcare professionals (HCPs), key opinion leaders (KOLs), as well as the steering committee members and study site staff involved with clinical registries. The individual will provide guidan

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Manager of Regulatory Affairs (RA) Labeling will assist in the development of a cross functional labeling strategy for products worldwide, including providing input on labeling requirements and strategic guidance duri

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

Create and approve regulatory content documents that drive artwork and labeling language Review and approve final artwork Manage preparation of regulatory documents for new product launches and maintenance of current products in the market with the correct alignment and compliance to regulations Maintain required regulatory compliance databases, systems and processes Supp

The Associate Chemist position is responsible for performing routine laboratory procedures in a quality control laboratory. Duties are performed under general supervision. Must be familiar with basic laboratory equipment and techniques. Responsibilities are focused on less complex testing and support functions. Key Responsibilities Performs routine testing of samples acco

Conducts release and stability testing of drug products following SOPs and cGMPs. Plans and executes validation of analytical methods. May develop and/or adapt methods. Solves more complex problems with some guidance from senior scientists. Troubleshoots instrumentation. May investigate new technologies. Documents results in ELN and RLIMS and performs second chemist revie

The Chemist is responsible for performing routine laboratory procedures in a quality control laboratory. Duties are performed under general supervision. Must be familiar with basic laboratory equipment and be able to demonstrate expertise in at least one essential testing technique. Responsibilities will include complex testing, support functions, and problem solving. Key

Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens. Analyze specimens using approved testing procedures. Review and release test results. Follow CLIA, HIPAA, OSH

In this role, you will serve as an individual contributor within a team; upon the direction and guidance of leadership, you will be responsible for supporting the goal of meeting scope, schedule and delivery requirements. Primary expectations of a Researcher I include Responsible for outreach, recruiting, screening, scheduling, and tracking of research participants Plans

The Research Fellow, Chemical Process Development coordinates activities in Active Pharmaceutical Ingredients (API) process scale up, process improvement and process optimization studies. The incumbent supports the transfer of technology to commercial manufacturing partners, monitors the manufacture of API and monitors stability data generated by Contract Manufacturing Or

Under supervision, performs laboratory analyses of raw materials, in process (IP), finished products (FP) and stability (ST) samples for pilot and submission batches, according to SOPs and cGMP procedures. Prepares method validation protocols/reports, and carries out method validation activities, including interim method validation, to meet project timelines. Supports lab