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  Saturday, September 18, 2004


   
 

Dear Life Sciences Professional,

DNAjobs.com is proud to feature the following jobs posted September 12 - 18. For each position, I have listed a short description and a link for more information.

As always, I wish you tremendous success in your searching!

Jason Skie

Manager - Clinical Quality Assurance

(US-California-San Francisco) Responsible for assisting the Director of QA in the development, implementation, and administration of quality assurance and quality control systems to ensure that trials are conducted and data are generated, documented (recorded) and reported in compliance with internal standards, GCP and applicable regulatory requirements.

Click here for more information.

Clinical Research Associate

(US-California-Oakland/East Bay) The primary purpose of the Clinical Research Associate (CRA) is to provide high-level assistance to the Senior Clinical Research Associate and the Chief Medical Officer as well as to the company in matters relating to the performance and monitoring of clinical investigations using the company's medical devices and procedures.

Click here for more information.

Senior Regulatory Affairs Specialist

(US-California-Silicon Valley/San Jose) Represent Regulatory Affairs Department at project development meetings. Form regulatory assessment for project release. Prepares 510(k), Letters to File, IDE, PMAs and their supplements for FDA review and approval. Assists in preparation, review and approval of Document Change Orders, especially those concerning device labeling and package inserts.

Click here for more information.

Quality Engineer II

(US-California-Oakland/East Bay) Actively participate in New Product Development Teams. Determine product quality requirements and generate Quality Plans. Direct Failure Modes and Effects Analysis and Risk Analysis activities. Determine Process Capability and evaluate process controls. Define and approve inspection requirements.

Click here for more information.

Senior Product Analyst

(US-California-Silicon Valley/San Jose) The Sr. Product Analyst investigates and resolves product complaints of all products and ensures all Medical Device Reporting (MDR) requirements are maintained. Works within the Complaint database, develops/maintains MDR database and complaint trend analyses.

Click here for more information.

Oracle Applications

(India-Chennai, Mumbai, Delhi, Bangalore) Over four years of IT experience, of which a minimum of two years should have been on Oracle Applications (10.7 / 11i) in a techno-functional role, with hands-on experience in manufacturing or financial modules. Should possess good programming skills on PL/SQL and reports. Overseas experience will be an added advantage.

Click here for more information.

Data Warehousing

(India-Chennai, Mumbai, Delhi, Bangalore) Over three years of IT experience, of which a minimum of 18 months should be on InformaticaPowercenter 6.x / Business Objects 6.x with Broadcast Agent and Supervisor tools. Candidates with experience in design, development and support of systems using Brio and Cognos will also be considered.

Click here for more information.

Microsoft Technologies

(India-Chennai, Mumbai, Delhi, Bangalore) Over four years of IT experience, with a minimum of two years on VB, ASP, .NET and COM. Knowledge of data storage, XML, XSL and XSLT will be an added advantage.

Click here for more information.

IT Project Managers

(India-Chennai, Mumbai, Delhi, Bangalore) Over eight years of IT experience, preferably in the telecom domain. Candidates should have thorough knowledge of SDLC and project management experience in at least three development projects. Should have excellent people management and customer interaction skills.

Click here for more information.

Regulatory Affairs Specialist

(US-California) Provide regulatory support for market-released products as necessary. Negotiate direct with FDA projects/products at reviewer level, as directed by manager. Assist with maintenance of Regulatory Affairs product flies to support compliance with regulatory requirements.

Click here for more information.

Senior Clinical Research Specialist

(US-California) Assist with overall successful conduct of assigned studies and assist in preparation of sections of the Investigational Plan. Assist in site activation (e.g. start-up document preparation, distribution, receipt, and review). Assist in preparation of study training materials and training of investigators, site staff and client field staff.

Click here for more information.

Group Leader - Cell Culture

(US-Connecticut-New Haven) A well established east coast biopharmaceutical company has an immediate need for a Group Leader-Cell Culture (Asst. Director level) to join their Bioprocess Development team. This position will direct the development and scale-up of mammalian cell culture processes for and transfer to GMP manufacturing of the companys therapeutic proteins and antibodies.

Click here for more information.

Scientist - Protein Chemist

(India-Karnataka-Bangalore) Should have industrial experience in the field of protein expression, purification, and characterization. Should be able to independently lead a research group. Experience in down stream processing in an industrial setup is preferable. Gangagen Biotechnologies is an early stage biotechnology company.

Click here for more information.

Senior Molecular Biologist

(US-Massachusetts) The applicant will work as a part of a multidisciplinary team responsible for the development & implementation of a novel DNA sequencing technology. It will involve development of applictions to suport sample preparation, amplification & genomic sequencing using molecular biology techniques.

Click here for more information.

Research Associate

(US-California-San Diego) GNF provides a unique and challenging opportunity to combine exploratory biomedical research with pharmaceutical drug development in a highly interactive, multidisciplinary environment and state-of-the-art facilities.

Click here for more information.

Senior Research Associate

(US-California-San Diego) The Genomics Institute of the Novartis Research Foundation (GNF), located in the Torrey Pines area of San Diego, CA, is funded by the Novartis Research Foundation and dedicated to the development and application of new methods and techniques for genome-wide biological discovery and biomedical research.

Click here for more information.

Pharmacology Group Leader - Research / Sr. Research Scientist

(India-Mumbai) As a key member of NCE discovery projects you will lead and direct a team of researchers evaluating in vivo efficacy of new molecules for metabolic and inflammatory disorders. You will be responsible for target selection/evaluation process, writing up project proposals, development of new in vivo pharmacological assay models and implementation of the projects.

Click here for more information.

Inflammation Biology Group Leader - Research / Sr. Research Scientist

(India-Mumbai) We are seeking a senior scientist in the area of Inflammation drug discovery. Candidate must be familiar with the general mechanisms involved in the inflammation and pathophysiology of inflammatory disorders. You should have a demonstrated expertise in cytokine signaling pathways involved in the pathogenesis of inflammation.

Click here for more information.

Cancer Biology Group Leader - Research / Sr. Research Scientist

(India-Mumbai) We are seeking a senior scientist with cancer-related drug discovery experience. In this role, you will be involved in identification, evaluation and implementation of new targets for screening in the area of cancer therapeutics.

Click here for more information.

Research Scientist - Bioinformatics

(US-California-San Diego) GNF provides a unique and challenging opportunity to combine exploratory biomedical research with pharmaceutical drug development in a highly interactive, multidisciplinary environment and state-of-the-art facilities.

Click here for more information.

Research Scientist - Medicinal Chemistry

(US-California-San Diego) The Genomics Institute of the Novartis Research Foundation (GNF) is funded by the Novartis Research Foundation and dedicated to the development and application of new methods and techniques for genome-wide biological discovery and biomedical research.

Click here for more information.

Group Leader - Staff Scientist

(US-California-San Diego) GNF provides a unique and challenging opportunity to combine exploratory biomedical research with pharmaceutical drug development in a highly interactive, multidisciplinary environment and state-of-the-art facilities.

Click here for more information.

Senior Product Manager

(US-California-Silicon Valley/San Jose) As a Marketing Manager within our neuro- marketing group, you will have responsibility for the global marketing of new and improved endovascular aneurysm devices. As a highly motivated and driven marketing professional, you will participate in the strategic decisions regarding future technologies and company growth.

Click here for more information.

Post Marketing Clinical Project Manager

(US-California-Silicon Valley/San Jose) Contribute to the development of client global marketing strategies and programs - working closely with senior members of Marketing. Develop US post-marketing clinical programs consistent with global strategies. Conduct post-marketing clinical studies. Lead and motivate the post-marketing team.

Click here for more information.

Biostatistician

(US-Massachusetts) Demonstrate broad expertise in statistics applied to clinical trials. Provides support to clinical trial working group teams and lead overall study analysis team, including protocol design, sample size and reandomizations, development strategy and coordination of SAS programmers.

Click here for more information.

Director of Research - Neuroscience

(US-Massachusetts) A creative, experienced scientist with extensive knowledge of neuroscience is sought to lead the Company efforts in neurometabolic and neurodegenerative disease research. In addition to managing the research and development activities of a group of neurobiologists, the individual will also be responsible for identifying new disease opportunities within the neuroscience area.

Click here for more information.

Director of Formulation Development

(US-Massachusetts) Start-Up and lead this effort for a Company with two compounds in phase 1 clinical development. RESPONSIBILITIES: The Director of Formulation Development will be responsible for developing solid and injectible dosage formulations for small molecule and peptide based drug products.

Click here for more information.

Regulatory Affairs Associates, Managers, Directors, Vice President

(US-Massachusetts) Positions exist for experienced CMC professionals. Positions exist for Advertising, Labeling and Promotion professionals. Positions exist for IND, NDA and / or BLA experienced professionals. Apply now for immediate consideration to see where your experience fits.

Click here for more information.

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