Biotech, R&D, Science category jobs

Our client is a leading research-focused healthcare group, in the diagnostics space. With continual organizational growth and strong pipeline, their regulatory affairs team is looking to bring in a new regulatory affairs principal specialist or manager. The Position: - Manages regulatory responsibilities associated with the development, support, and manufacturing of the Company's medical device pr...
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An opportunity exists for an exceptional individual in the area of biopharmaceutical product performance. Wolfe Laboratories conducts rational formulation development that leverages a molecular understanding of the pharmaceutical and biopharmaceutical attributes for the delivery of drugs, including poorly soluble drugs, via conventional and non-conventional oral formulations as well as complex par...
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The Core Evaluation Specialist I position, will be responsible to test, process and analyze geological samples. Duties to include: compile and record testing and prepare operational data using laboratory testing equipment. Also, ensure that products meet quality standards. Able to work in a team environment and practice close attention to details. Perform various other duties, projects and activit...
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Responsibilities include: Medical review, which involves in-house review of Case Report Forms (CRFs) including query resolution and addenda writing, QA of data listings. May manage the activities of regional contract CRAs, and organizes the files and budgets associated with several clinical studies. Provides medical support which may include: Adverse Event Reporting - the investigation and reporti...
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JOB SUMMARY: We require a highly motivated Research Scientist to work on protein stability & aggregation as it relates to therapeutic protein development. The current project is designed to understand the fundamental mechanism/s of protein instability, sub-visible particulate formation and aggregation using variety of chromatographic, biophysical and biochemical tools. DUTIES AND RESPONSIBILITIES:...
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Position Overview Perform and coordinate all aspects of the clinical monitoring process in accordance with GCP and global SOP to assess the safety and efficacy of investigational products and/or medical devices. Conducts site visits to determine protocol and regulatory compliance, and prepares required documentation. Represents company in the global medical research community and develops collabor...
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Currently we are assisting large research facility to provide contractor assistance pertaining to physiological research of crop plants. Overview of position entails preparing seeds for planting, transplanting, watering, and maintaining healthy plants in greenhouses and/or growth chambers. Will assist senior management with measuring, harvesting, sampling, and processing plants and plant tissues f...
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Contract hire will be responsible for testing and interpreting results for raw materials, active pharmaceutical ingredients, finished pharmaceutical products, and stability samples. With an expertise in laboratory techniques commonly used in the analysis of pharmaceutical products, this position will help to ensure that suitable methods are in place to evaluate samples using equipment to analyze, ...
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DESCRIPTION: · Performs a variety of qualitative and quantitative analytical assays to support raw material, in-process, intermediate and final product testing according to standard operating procedures and regulatory requirements. · Performs laboratory operations necessary to support testing, such as reagent preparation/qualification, equipment and assay troubleshooting. Analyzes results and noti...
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If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International has one of the largest global footprints ...
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Primary Responsibility: · Research and develop advanced techniques and tools to reliably measure and monitor electrical properties of semiconductor and solar grade silicon wafers. · Research and develop advanced electrical metrology techniques and tools to improve the detection limits of impurities and defects in and on silicon wafers · Lead in evaluating and improving metrology used in the polysi...
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Provide and carry out various Epidemiology group deliverables. These may include: o Consult on / authoring of regulatory responses and participation in regulatory meetings related to safety or risk assessment o Safety epidemiology literature reviews supporting regulatory meetings, interactions, submissions (e.g. Epidemiology sections of the Risk Management Plans (RMPs), Pediatric Investigational P...
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BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QC Assay Associate to work for a leading Orange County biotechnology company. QC Assay Associate We currently have a need for a QC Assay Associate - Temp in the QC department covering for someone who is out on a leave of absence for 6 months. Pay ra...
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Responsibility The biostatistician will provide statistical support in the clinical research, including monitoring / querying data from the database, executing the statistical analysis, providing statistical reports, validating statistical analysis and writing/reviewing the statistical part in the final study reports. The statistician may also be involved in reviewing research protocol drafts and ...
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Description: · Performs a variety of qualitative and quantitative analytical assays to support raw material, in-process, intermediate and final product testing according to standard operating procedures and regulatory requirements. Performs laboratory operations necessary to support testing, such as reagent preparation/qualification, equipment and assay troubleshooting. · Analyzes results and noti...
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Fleet Laboratories, a leader in innovative personal health and beauty care products, has an immediate opening for the following position at our international corporate office and manufacturing plant located in Lynchburg, VA. Senior Microbiologist 1st shift The Senior Microbiologist assures the microbiological quality of raw materials, bulk products, finished products, R&D development and stability...
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Our client, a global leader in the pharmaceutical industry, is seeking a Clinical Research Associate to join their Jacksonville, FL, location. This is an on-site position The CRA will plan and monitor human clinical trials in compliance with internal procedures, ICH Guidelines, Good Clinical Practices (GCP) and applicable Regulations and Guidelines. Responsibilities will include: · Coordinate prot...
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Smithers Viscient is a member of The Smithers Group, an independent global leader in delivering trusted solutions by integrating science, technology, and business expertise. Our companies are innovative in adding value throughout the life cycle of our clients’ products utilizing testing, consulting, information and compliance services. Backed by a strong reputation and years of experience, every S...
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Will join the new Klarman Cell Observatory at the Broad Institute with the mission of systematically defining cellular circuitry. The goal of the observatory is to tackle one of the biggest challenges in biology: mapping the molecular “circuitry” inside several kinds of mammalian cells and will spearhead an International Human Circuits Project-that would chart the molecular and genetic connections...
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The selected candidate will support multiple projects, ensuring they are executed and completed within established timelines and budget. Required Qualifications: Bachelor’s Degree 2-5 years experience and understanding of the pharmaceutical industry Exceptional oral and written communication skills Exceptional technical skills, including MS Project, SharePoint, PowerPoint, etc PMP Certification pr...
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The Director, Project Management works effectively across multiple divisions to direct the delivery of projects within cost, time and quality requirements. May provide direct supervision, support, training and mentoring to project managers. Works with leadership in all functional areas on the continuous development/improvement of business processes to support cross functional teams and to ensure t...
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Functional Unit Scope: o GRD provides regional and country regulatory development expertise and leadership, driving strategic local/ regional and global execution and operational excellence in achieving key product development milestones for clients o Team of regulatory experts delivering regulatory project development milestones and dossiers, excellence in navigating regulatory environment, requi...
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Description: · The Scientist will support formulation and manufacturability for a broad range of consumer products such as Skin Care, Beauty Care, Oral Care, Wound Care and Women’s Health Care. · Lab batching for various consumer products · cGMP lab notebook documentation · Measuring Brookfield viscosity, pH and aesthetic monitoring of stability samples · Writing specifications and working within ...
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Overview: It is important that this individual have Clinical Trial Manager experience, and preferably global experience and has worked with Asia Pacific. As a key member of the clinical operations team working on a Hemophilia Therapeutic Area, this individual will play a critical role in advancing our hemophilia programs on a global basis with the overall goal of significantly improving treatment ...
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When it comes to "clean," Ecolab is the world leader, with $5.5 billion in global sales and the respect of customers in more than 160 countries. For eight decades we have developed and marketed cleaning solutions and systems making the world a cleaner, safer, healthier place to live. More than 26,000 Ecolab associates are winning and satisfying new customers every day all over the world. Are you a...
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