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Global Pharmaceutical Company out of Madison, NJ and Irvine, CA Position Summary: (Irvine, CA or Madison, NJ) Responsible for leading internal and outsourced Clinical Programming activities in support of Clinical Research studies and managing the design, development, validation, implementation, and oversees ongoing support to electronic case report form (eCRF) systems (e.g. InForm, etc.), external data acquisitions, reporting/business intelligence tools (e.g. SpotFire, J-Review), and other....


Global Pharmaceutical and Medical Device company is expanding and in need of a Senior Manager, Process Improvement (manufacturing) New role- must have six sigma and experience in process improvement Must have manufacturing experience, Must have proven change management Must have a very good personality and strong communication skills to effect change with executives but also be relatible to the people at the manufacturing sites Salary is 100k-130k Will relocate , 15%bonus and full benefits....


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....

- Greenville, SC

Diverse Pharmaceutical company A rated expanding-Supervise Maintenance professionals toward the ultimate objective of uninterrupted plant operations and support of capital improvement projects. Must be willing to work off shift hours Responsibilities Responsible for the implementation of the work order, Preventive Maintenance and Supply Room programs. Responsible for HVAC systems. Responsible for assuring that sufficient levels of equipment spare parts, stored fuels, chemicals and other....


Major Pharmaceutical and Manufacturing company is looking to hire 6 Production Line Operators - Sterile Fillers for a contract w-2, full benefits start in December and goes to April or May (and can then be renewed) $16-18/hour Must be able to work overtime and third shift All Production Line Operators (Sterile Fillers) are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. Must have....


Global Pharmaceutical company with US Headquarters in Chicago area of Illinois and Boston area of Massachusetts is adding to their team in Deerfield, IL Looking for Project Manager for their Sales/continuing education department PMP preferred 6 month full time contract and then up for renewal $45-50/hour, w-2, health benefits and more Local candidates only OBJECTIVES: - Deliver project objectives within time, resource, and budget constraints - Build and maintain collaborative relationships by....

- Clearwater/St. Louis, MO, FL

Assistant or Associate Director, Regulatory Affairs- Medical Device/CMC Position can be located in either the St. Louis, Missouri office or their Clearwater, Florida office relocation is provided Candidate MUST have Medical Device experience and must have written CMC submissions in the past (recent past is preferred) Individual Contributor role Specialty and Diverse Pharmaceutical company is adding to their high profile team competitive base salary, plus bonus, full benefits and other Long....

- Greenville, SC

Beautiful Greenville, S.C.has a strong Global Pharmaceutical company that is looking for a Validation Engineer (or Senior Level) - Validation/ Process Engineer full relocation and full benefits ResponsibilitiesRemain current on cGMP practices for Process Validation and ensure local Process Validation SOPs and validation documents reflect current industry practices.Provide validation requirements, strategy, protocols, execution and final reports for changes impacting validated products and....

- Stephenville, TX

Put your career on track with this multibillion dollar international food company. Get in on the ground floor and grow grow GROW! Looking for individuals with a BS degree in Science, Engineering or Business. You need to have a minimum of an internship in a food manufacturing setting. One to three years operations or in-plant quality experience is preferred. Please note that you will need to be open to relocation and working all shifts. A full relocation package is provided. This position....

- Logan, UT

Put your career on track with this multibillion dollar international food company. Get in on the ground floor and grow grow GROW! Looking for individuals with a BS degree in Science, Engineering or Business. You need to have a minimum of an internship in a food manufacturing setting. One to three years operations or in-plant quality experience is preferred. Please note that you will need to be open to relocation and working all shifts. A full relocation package is provided. This position....

- Harrisburg, PA

This position REQUIRES a four year college degree. There are NO EXCEPTIONS! Put your career on track with this multibillion dollar international food company. Get in on the ground floor and grow grow GROW! Looking for individuals with a BS degree in Science, Engineering or Business. You need to have a minimum of an internship in a food manufacturing setting. One to three years operations or in-plant quality experience is preferred. Please note that you will need to be open to relocation and....


US Medical Leader will be the single point of accountability and matrix leader for US Medical strategies, including US launch and life cycle management for a oncology. Reporting the US Head of Oncology Medical Affairs this US Medical Leader will lead the development, execution and communication of the US Medical Team. This person will be the driver and point of contact for internal and external stakeholders. This company has strong and diverse pipeline in oncology. It is preferred that this....


Job DescriptionAssists with the development and maintenance of the Enterprise Resource Planning (ERP) system. Responsible for database administration, data consolidation, data analysis and management reporting. Utilizes software to generate metrics and develop actionable recommendations. Customizes and configures workflow to allow the integration of client/server applications. Evaluates ERP systems to ensure the system is meeting corporate needs. Knowledge of standard concepts, practices, and....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they are adding a new Field Service Engineer to be based in Boston or Albany, NY or Hartford, CT. Requirements:The preferred candidate will have an A.S. or B.S. in electronics engineering or Chemistry or equivalent as well as experience in the calibration, troubleshooting and repair of complex electronic instruments.The client will look at....


Global Pharmaceutical company with high profile trials is expanding and looking for a Director, Regulatory Affairs for their Global Management Team Competitive base salary and bonus, full relocation and benefits, Long Term Incentives and more Position IDEALLY is located in the Cambridge, MA office (there is small possibility the role can be based in their NJ office) The Rare Disease Global Regulatory Team Lead (GRTL) is part of the Global Regulatory Affairs (GRA) team based in the US. He/she....


Traditional SHE leader's role dealing with a Chemical manufacturing facility. MUST HAVE PSM BACKGROUND AND EXPERIENCE. Will not even look at anyone without it. Lead the plant’s safety, health, environmental and security programs, as well as the operation of the Utilities function. Take the lead on all compliance with all safety and environmental regulations and policies. Lead effort in compliance with environmental regulations, permits and reporting requirements. Responsible for the operation....


Product Development Chemist/ R&D Director - expert in Ion-exchange (IX) technologies in liquid purification Location: North, NJ – near Edison, Little Falls, Newark NJ (with Great relocating benefits provided.) The Product Development Chemist will have a “director” title in a well-established company. As “Director of R&D” you’ll be a senior level technical expert help bring our client “into the future” - to the next level of innovation in ion-exchange purification technologies with a....

- Canton, OH

Small employment law firm seeks an Office Manager. The ideal candidate has demonstrated AP/AR skills (including QuickBooks); can effectively manage and lead a staff; work well with the firm's attorneys; be the liaison for vendors; and handle general office administration. A professional, positive, and team player attitude is a must. Compensation dependent on skills and experience. Law Firm administration and accounting experience preferred but not a must. Required experience:Office Management:


This Chemist position will report to the Technical Director in the Quality Control/R&D Department.Summary:Responsible for formulating new products, reformulating existing products, qualifying alternative raw materials, reviewing and/or updating manufacturing procedures, setting up test methods, and laboratory equipment. This position interacts with Quality, Production, Sales, Customer Service. and Purchasing Departments.Essential Duties and Responsibilities:Conduct Research and Development

- Milwaukee, WI

Excellent oppt'y for a Medical Technologist to work for a medical lab instrument manufacturer and utilize their lab knowledge as a Technical Support Specialist. Will be instrumental during the installation process as a trainer, and documenting the lab procedures. This position can be based almost anywhere in Wisconsin as long as you are within a 45 minute to 1 hour drive from a major airport.Will also be involved with direct problem solving covering reagents, kits, procedures, adaptations, and

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