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- Charlotte, NC
new job!

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....


We are looking for a Technical Services Scientist who will be responsible for working on all aspects of the technology transfer for sterile drug products, specifically Lyophilized and vial products, pre-filled syringes, and Blow-Fill-Seal (BFS) products. This would include working with Formulation and Analytical Development, Quality, Production and Regulatory to identify product and process criticalities and how to maintain them along with finding creative solutions to any roadblocks in the....

- 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....


Here is an excellent growth opportunity with a prominent food products manufacturer! Plant Sanitation Manager -- Cleveland, OH -- 6 day week (6 days, 10 hours per day) -- $78-85,000 -- Excellent benefits -- Relocation Assistance Responsibilities of the Sanitation Manager: - Manages the company's sanitation department. to requirements for food processing machinery, equipment, and facility - Includes assisting in planning, scheduling, assigning and directing of sanitation personnel (approx:....


Senior Analytical Chemist Location: Rockland County, NY (Near Ramapo, Nanuet, & Tappan NY and Park Ridge NJ) Unable to publish the full confidential salary range but we can talk about it! ( I filled in the low salary box but not the high level) An opportunity for a Senior Lead Analytical Chemist to support a process development effort. This is a critically important position since ‘reliable data’ is a key to success as they work to develop a novel process. The position will include a....


POSITION SUMMARY: The Principal Scientist is responsible for method transfer/method verification/co-validation of compendial and non-compendial analytical methods utilized across the company according to written procedures. The testing of routine and non-routine samples where specialized training is essential. Planning and coordination of method transfer/method verification activities in the transfer of analytical methods from the Product Development department or between its facilities.....


Essential Functions: - Knowledge and experience in technologies such as continuous processing, flow chemistry, microwave chemistry is preferred. - Knowledge of and experience with in-situ reaction monitoring technology is preferred. - Knowledge or expertise in principles of operational excellence, six-sigma, and process optimization preferred. - Application of key principles of chemical engineering to work within a matrix-based chemical development team to construct systems and design chemical


Summary We are currently accepting resumes for the position of Research Scientist in Analytical R and D/Methods Development and Validation. ResponsibilitiesMust be fully capable of developing analytical methods based on experience, literature search, etc.Design, develop, conduct and/or review experiments including method development and methodtransfer; perform methods validations utilizing typical instrumentation including but not limited to LC,MS, GC, etc.Interpret data from routine and....


My client, a highly regarded New York based research consortium has asked us to search for a Director to lead biologics drug discovery projects in collaboration with academic investigators. You’ll be responsible for lead identification of therapeutic antibodies and proteins, in order to efficiently advance complex research programs from early target validation through animal proof of concept studies. They want a PhD in Immunology, Pharmacology, Molecular or Cell Biology, Biochemistry, or....


Our client is comprehensive education consulting company that works with governments, education providers, industry, unions, parents and communities in private and public school management to drive improvement. They have positioned itself with to work with multiple stakeholders to deliver fast, dramatic improvement of education. The consultancy offers a comprehensive array of services from school and system transformation to teacher training and cutting-edge learning enhancement. These....

- New York, NY

My client is in start-up mode seeks a Director to oversee clinical research and drug safety activities along with clinical research strategy. The ideal candidate will take on the following tasks:Oversee clinical study activities.Recruit, manage and develop a small clinical research and drug safety team.Oversee data analysis, evaluation and reporting of clinical data including study reports, FDA and ethics committee progress/final reports, and assist with manuscript preparation.Forecast....


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 client seeks a Computational Chemist Post Doc to study molecules and prepare safety assessments on materials and natural complex substances. The ideal candidate will take on the following tasks:Use modeling and in-silico sources to derive data to support risk assessments for molecules.Work closely with a group of toxicologists, safety assessors, and other scientists to ensure molecule safety.Identify clusters and scientifically valid read across materials to complete endpoint....


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....


Global Pharmaceutical company is looking for a Clinical Partnership Liaison Must have pharmaceutical, Biotech or CRO experience at this senior level. located in NYC must work in the office three days/week The Partnership Liaison is a key leadership role within Clinical Operations Business Operations Management. The role is responsible for implementing and driving the success of the Clinical Development sourcing strategy. The role is accountable for Clinical Development alliances with clinical....

- Jersey City, NJ

Pharmaceutical company in Jersey City, NJ in need of Clinical Research Associate Responsible for monitoring of single and multi-site clinical trials. Assures adherence to international Commission on Harmonization (ICH), Good Clinical Practices (GCP), and Code of Federal Regulations (CFR). Assures compliance with institutional Standard Operating Procedures (SOPs) and Policies, protocol requirements, and institutional reporting requirements. Performance of this position requires coordination and


Global Pharmaceutical company is hiring a GLOBAL HEAD RESOURCE MANAGEMENT AND ANALYTICS Position Purpose: Leadership role in Business Operations Management in Clinical Operations with strategic oversight and accountability for the delivery of all aspects of resource planning, capacity management & analytics (metrics) within Clinical Operations.Propose, deliver & implement resource strategies, processes, analyses and tracking for the provision of resource management information to....

- Any US State

Global Pharmaceutical company is hiring Clinical Project Manager for their Clinical Development studies Day to day management of studies This position is responsible for providing oversight of Phase 1 to Phase 4 clinical trial implementation; ensuring clinical studies are conducted in a timely manner with milestones being achieved within budget.Essential FunctionsThe Clinical Project Manager for this Pharmaceutical company- will:Utilize Project Management techniques and methodologies to plan,....


Director, Medical Information for this leading pharmaceutical company in New England S Headquarters in Waltham, MA Looking for Senior Engineer for drug product unit operations- leadership scale-up and optimization in development from R&D to cGMP Phase 3 manufacture to process validation. Experience with continuous manufacturing, scale-up and PAT implementation is strongly desired. The individual is expected to integrate QbD principles, guide experimental design with a focus on process....


Top Tier Pharmaceutical company (with focus in RESPIRATORY, CNS, Diabetes, Cardio, GI and more) in Madison, NJ is looking for three Clinical Trials Manager Consultants for Clinical Trials Group This is a one year contract and can continue for up to 4 years (1099 or w-2)SummaryParticipate in all aspects of clinical development and study management under the direction of the Director, or designee, which includes providing scientific, and/or logistical support to planned and ongoing trials CTM –....

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