Biotech Jobs in Ocean View, Delaware

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Hello, My name is Derick and I represent The Fountain Group. We are a national staffing firm and are currently seeking Chemist for a prominent client of ours. This position is located in Wilmington, DE. Details for the positions are as follows: Job Description: Performs qualitative and quantitative chemical analysis of raw materials. Coordinates testing responsibilities to ensure QA test support a...
Please note this is a 8 months contract position. Skills: QA Test experience, Auditing experience, Medical Device or Pharma Industry Performs qualitative and quantitative chemical analysis of raw materials. Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. Functions as a team member in the QA Chemical Laborat...
My name is Paige, and I represent The Fountain Group. We are a national staffing firm and are currently seeking a candidate for a Chemist position for a prominent client of ours. This position is located in Wilmington, DE. Details for the positions are as follows: MUST BE FLEXIBLE FOR 2ND AND 3RD SHIFTS (2pm-10:30pm and 10pm-6:30am) Performs qualitative and quantitative chemical analysis of raw ma...
Job Description Fast-growing global developer and manufacturer of Pharmaceutical API’s is seeking a Quality Control Manager. In this key position you will be responsible for the following: Supervise all QC laboratory functions Approves laboratory deviations Reviews and trends product data for APR and process improvements Sets priorities within laboratory based on production schedule Assures lab co...
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As a SSU you will be responsible for the independent preparation, review and approval of country related submission packages in accordance with ICH, GCP and all applicable regulations, laws...
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Senior Specialist Surveillance Job ID: 629 Industry: Biotech/Pharmaceutical Location: Wilmington, DE Duration: 9 Month Contract Pay Rate Range: Depends on Experience (W-2 all incl...
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Global Quality Specialist Job ID: 611 Industry: Biotech/Pharmaceutical Location: Wilmington, DE Duration: 7 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive...
Our client, a Pharmaceutical Company in King of Prussia, is looking for an experienced Project Manager for a contract role through 2014. Responsibilities: Overseeing a Mobile Device Project for IPad' s. Responsibility for all aspects of the project over the entire project life (initiate, plan, execute, control, close). Assigning individual responsibilities, identifying appropriate resources needed...
This position requires someone with an associates or bachelors degree in Medical Technology Clinical Laboratory Science. The person will be operating Clinical Chemistry analyzers to verify their reliability. These instruments perform medical diagnostic tests (Basic/Comp panels, liver/cardiac panels, lipids, drug monitoring, drugs of abuse, etc.) on pseudo patient samples. Day to day task involves...
Job Title: Safety Surveillance Specialist Duration: 6 months Location: Wilmington, DE 19850 Manage safety data using analytical skills, processing adverse event cases of all levels of business risk and/or providing scientific or technical input to Surveillance or Support section activities. Senior specialists require effective project management skills to deliver a project or piece of work for Cli...
Provides technical and/or systems support in the global quality function. Works independently and in cross-functional groups . The job holder communicates frequently with various levels of management (including senior management) in different functions. May be required to carry out complex quality and technical project work. • Liaise with Suppliers to ensure successful delivery of projects / suppl...
Provides technical and/or systems support in the global quality function. Works independently and in cross-functional groups . The jobholder communicates frequently with various levels of management (including senior management) in different functions. May be required to carry out complex quality and technical project work. • Liaise with Suppliers to ensure successful delivery of projects / suppli...
Title Senior Scientist, Health Economics and Outcomes Research Description Description: The Senior Scientist, Health Economics and Outcomes Research (HEOR) will have responsibility to interact with Organized Customer Group Directors and Leaders within brand teams and with Medical Affairs to design and implement innovative Real World Evidence(RWE)/HEOR strategies and activities and to produce (or d...
• Operational responsibility to set-up the local Trial Master File (eTMF) and Investigator Site File including tracking of documents. Maintain and close the local TMF (in electronic or paper form depending on study) ensuring International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) compliance and local requirements. Support the CRA in the maintenance and close out a...
On behalf of Research Triangle Institute, Headway Workforce Solutions is seeking part time Field Staff to work on a government sponsored research study in New Castle County. Candidates must live close to the coast. POSITION SUMMARY RTI International is seeking to hire field interviewers for the Access-Point Angler Intercept Survey. This important research study, sponsored by the National Oceanic a...
Description: This role will be based in Wilmington, DE. An ideal candidate should have significant experience in pain management and would thrive on proactively engaging internal and external leaders and will serve as a medical expert for their brand and disease area. The ideal Medical Director will also have strong commercial aptitude and/or experience, including proven ability to translate and a...
To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with company Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. In addition to leading LST(s), LSTL is expected to perform site monitoring if needed. As part of the flexible capacity...
The Programme Manager will manage and implement key initiatives within the non-profit Foundation, including the program which provides grants of $150,000 and up to US-based nonprofit organizations working to improve cardiovascular health in the United States. This role will be responsible for day-to-day program administration and implementation to increase the Foundation’s operational efficiency a...
Regulatory Affairs Manager Location: Wilmington, DE Description: Prepare and deliver regulatory operational plans for allocated projects/products. Contribute to solutions to regulatory issues. Project manage quality regulatory submissions to agreed project targets. Provide operational regulatory input and guidance in cross-functional teams. Work flexibly within and across Therapeutic Areas to prov...
Title Medical Director US MA Patient Safety Description Medical Director US Medical Affairs Patient Safety - 2 Positions Open The role holder provides medical leadership as either an expert lead for a number of drug projects that ensures effective collaboration between physicians and teams. Will develop and build, or act as a safety medical expert, within a cross-functional multi-skilled team comp...
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