Quality Control Manager JOB FUNCTION/PURPOSE Quality Control Manager in support of the test and release for API manufacturing as well as analytical chemistry activities DUTIES AND RESPONSIBILITIES Principal Responsibilities (including Technical Responsibilities where appropriate) Overall supervision of senior scientists, scientists and associates includes direction of group activities as necessary, resolution of problems/issues with QC and internal and external clients. Prepare performance reviews of direct reports. Provide performance reviews in both oral and written form to direct reports.

Manager of Clinical Data Management Summary  Provide leadership and expertise in data management for clinical trials.  Serve as the lead collaborator for a range of projects that require data collection and data management.  Ensure data integrity and security for clinical trials and projects, including projects that are contracted to Contract Research Organizations (CROs).

NextGen is a premier consulting and permanent placement organization focused on hiring talented professionals.  Currently we are seeking qualified individuals in St. Louis, MO for a Scientific Software Application Tester.

This position is open as of 12/19/2009. Senior Regulatory Affairs Specialist - Class III Medical Device - Bay Area Senior Regulatory Affairs Specialist - Medical Device - Bay AreaWe develop, manufacture and market catheters for both the coronary and peripheral interventional markets. We are backed by several venture capital firms and have distribution of our catheters in over 10 EU countries as well as several in Scandinavia and the Asia/Pacific region.

Summary: Responsible for overseeing all aspects of research pertaining to Materials by assuring that all performance, technical, administrative, staffing and scheduling targets are met. Essential Duties and Responsibilities: Evaluate and select appropriate research projects for commitment of organization resources Review and analyze proposed projects to determine if benefits derived and possible applications justify expenditures and human resources Coordinate all aspects of research and development proposals (such as objective or purpose of project, applications that can be utilized from findings, costs of projects and material equipment, and human resource requirements) Develop and implement methods and procedures for monitoring projects (such as preparation of records expenditures, and research findings, progress reports, and staff conferences) in order to inform management of current status of each project Recommend measures to improve methods, performance, and quality of product Write and maintain department procedures to assure documentation for all areas of responsibility Perform all other duties as assigned Supervisory Responsibilities: Directly manages R&D staff and is responsible for the overall direction and coordination of work Qualifications: Must be able to perform each duty outlined above and possess the education, skills, and abilities described in this job description Education and/or Experience: A master??

This position is open as of 11/9/2009. Principal Scientist - R&D Manager - Molecular Assay Development Principal Scientist - Molecular Assay DevelopmentThis is a fantastic opportunity for a Diagnostics Research & Development Scientist responsible for planning, organizing and performing experiments to develop state-of-the-art assays.What you need:- Ph.

Regional Clinical Research Associates Levels I, II, and Seniors ...

Scientist/Modeler/Pharmacometrician   My client has an established global team of scientific, clinical and technical experts dedicated to using model-based drug development (MBDD) to strengthen the quality, visibility, and value of critical development decisions. This is to work for a stable leader in consulting the pharmaceutical industry   DESCRIPTION:   My client’s internationally renowned scientists, modelers and biostatisticians help pharmaceutical companies develop drugs in all therapeutic areas more quickly, efficiently and successfully.     PLEASE DO NOT APPLY UNLESS YOU HAVE THE FOLLOWING:   PhD or MD equivalent in Statistics, Clinical Pharmacology, Biopharmaceuticals, Biochemistry, Decision Science, Pharmaceutical Sciences, etc … Minimum of 3 years industry experience in areas such as mathematical modeling and simulation, drug development, population PK/PD and statistical modeling.

Manufacturing Supervisor Our pharmaceutical client is looking for Production Supervisors to supervise all manufacturing tasks required for the safe production of solid and liquid dosage environments in compliance with FDA, DEA, OSHA Federal, State, and Local regulations. The primary objective of this position is to ensure that all manufacturing operations are conducted in a safe manner and in compliance with all applicable cGMPs' and DEA requirements. Working flexibly across a broad range of chemical operations and participation on self-managed work teams is required.

Scientist/Modeler/Pharmacometrician   My client has an established global team of scientific, clinical and technical experts dedicated to using model-based drug development (MBDD) to strengthen the quality, visibility, and value of critical development decisions. This is to work for a stable leader in consulting the pharmaceutical industry   DESCRIPTION:   My client’s internationally renowned scientists, modelers and biostatisticians help pharmaceutical companies develop drugs in all therapeutic areas more quickly, efficiently and successfully.     PLEASE DO NOT APPLY UNLESS YOU HAVE THE FOLLOWING:   PhD or MD equivalent in Statistics, Clinical Pharmacology, Biopharmaceuticals, Biochemistry, Decision Science, Pharmaceutical Sciences, etc … Minimum of 3 years industry experience in areas such as mathematical modeling and simulation, drug development, population PK/PD and statistical modeling.