DNAjobs.com is proud to feature the following jobs posted December 17 - January 1. 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
Research Associate in Bio-Health Informatics
(UK) The successful applicant is likely to possess a postgraduate qualification and will have experience of one or more of the following; the application of informatics tools for DNA and protein sequence analysis and homology searching, of XML and data modelling techniques, the statistical analysis of transcriptomics and proteomic data, and the functional annotation of large-scale gene/EST collections.
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Gene Sequence Data Analyst
(US-Utah-Salt Lake City) Analyze patient data output from genetic sequence analyzers for use in DNA typing and identification. This person will assist in diagnosis of predisposed risk of Breast, Ovarian, Colon, and other cancers or analyze data for DNA fingerprinting to assist in Forensic applications. Must maintain all appropriate documentation of analytical data.
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Research Scientist - 2 Positions
(India-Orissa-Bhubaneswar) Research Scientist: M.Sc./Ph.D. in Life Sciences with 2-3 years experience in mammalian cell culture and maintenance of mammalian cell lines. Prior experience in biotech industry is preferred. Research Scientist: M.Sc./Ph.D. in Life Sciences or Chemistry with 2-3 years experience in antibody conjugation to different fluorophores and purification of antibodies using peptide affinity column.
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Research Assistant
(India-Orissa-Bhubaneswar) Research Assistant: M.Sc. in Biological Sciences with laboratory experience in immunological and molecular biology techniques. The successful applicants will be part of a research team that develops monoclonal and polyclonal antibodies, tissue arrays, and novel kits for use in biomedical research.
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Forensic DNA Technician
(US-Utah-Salt Lake City) This position will be responsible for performing certain aspects of forensic DNA analysis procedures on criminal casework samples with emphasis on instrument and/or robotic operations. This position will work closely with the forensic team to accomplish our mission and may train other staff as necessary.
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Formulation Research Associate / Scientist
(India-Karnataka-Bangalore) Qualification: M.Pharm/Ph.D in Pharmacy. Experience: 5-8 Years. Location: Bangalore. Other Information: Experience in animal toxicity studies and pharmacokinetics desirable.
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Senior Service Engineer
(India-Mumbai) Electronics Engineers with 2 to 3 years experience servicing sophisticated biotechnology / scientific instruments, viz., Liquid Chromatograph, Mass Spectrometer, Thermal Cyclers, etc.
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Director Quality Control
(US-California-Orange County) Coordinate finished product stability testing, the purchase and QC of new lab equipment. Supervise the development of new analytical methods, all equipment repair and preventive maintenance. Write/review/approve: SOPs, validation protocols, QC deviations, reports for and analytical methods. REQUIREMENTS: Masters or PhD in analytical Chemistry or related field.
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Research Associate
(US-Utah-Salt Lake City) The responsibilities include the development of sophisticated clinical molecular genetic tests and forensic genetic assays. These assays are implemented on highly automated processing platforms. All development activities require extensive documentation due to the nature of the specimens.
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Testers
(India-Karnataka-Bangalore) Total experience of 3+ years in testing. Software development experience of 6 months to 1 year desired. Should have experience in client-server. Should have experience in web based application testing, at least on large projects. Should have very good exposure to RDBMS like Oracle/SQL. Automated tools exposure desired.
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Java Developers
(India-Karnataka-Bangalore) Must have at least 3+ years of software development experience. Strong experience with Internet development technologies, like J2EE, Struts, RMI, JMS, XML and Servers: Weblogic/Websphere, JRun. Strong RDBMS knowledge. Strong design/development experience with 3-tier component-based applications.
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C++ with Oracle Database
(India-Karnataka-Bangalore) Must have at least 3+ years of software development experience, preferably commercial database applications utilizing C++ and Oracle. At least 2 years experience in developing large, preferably commercial applications in the Web environment. Internet based application development using C++, VC++, MFC, COM, RPC, Win32, STL, Roguewave, XML.
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Faculty Position
(US-Kansas) Applicants must be committed to both teaching and research. Applicants should have a PhD degree in computer science with demonstrated expertise in Bioinformatics; salary will be commensurate with qualifications. Applications must include descriptions of teaching and research interests along with copies of representative publications.
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Project Lead IS Site Coordination
(US-Massachusetts) Manage an approved and funded program of a work in support of a new scientific effort in chemogenomics, to assure smooth implementation and progression of CGC business goals and objectives. Coordinate and align all internal IS-related activities for functions and associates working on IS-related activities at the CGC.
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Project Leader Development
(India-Karnataka-Bangalore) Total experience of 5+ years Software development experience desired in C++/JAVA. Should have experience in client-server. Should have experience in web based application. Should have very good exposure to RDBMS like Oracle/SQL. Should have lead the team. Should have done requirement gathering.
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Technical Writers
(India-Karnataka-Bangalore) Minimum of 2 year as a technical writer. Expertise in Microsoft Office Product Suite. Excellent skills in written and spoken English. Qualification: Any Graduate preferable in English Literature.
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President and CEO
(US-Connecticut) The mission is to guide the continuing growth and development of the Company. This includes managing existing operations, insuring the success of existing partnerships, driving the development of products currently in the pipeline, creating a U.S. based corporate presence, raising the Company profile with the investment community and attracting additional capital.
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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.
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Sr. 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.
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Head Pharmacology
(India) Should be Ph.D with Pharma back ground in the field of Pharmacology / Pharmacokinetics with strong scientific background in VITRO and IN VIVO pharmacology. Expertise for cell biology, molecular biology and biochemical techniques in Drug Discovery. Should be able to assist clients in study and data interpretation and reporting.
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Sr. Manager - Marketing
(India) Candidate shall essentially look after and promote our business interest in US and grow our business further. He/she will coordinate with our existing customers on a regular basis to expand business volumes. In addition, he/she will create new business opportunity through identification of new business partners, new pharmaceutical services and products.
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Manager / Sr Manager - Business Development
(India) Candidate, should be a Ph.D. in Organic Chemistry / Biochemistry / Medicinal Chemistry, preferably a post-doc from US itself. Besides having experience of working as a scientist, candidate should have some experience in outsourcing / Business Development preferably of Pharmaceutical services / contract research offerings.
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Bioinformatics
(India) Ability to lead software developers in design, development and testing of web-based bioinformatics applications. Good knowledge of Bioinformatics public databases and technologies - from comparative Genomics to microarray analysis.
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Nurses (CGFNS, IELTS Cleared)
(UK/USA/Australia) We require Nurses (IELTS and CGNFS cleared). Please respond with your Current Resume, Current Location and Current Company if you meet the requirements.
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Speech Therapists
(UK/USA/Australia) We require Speech Therapists (Masters, TOEFL & TSE Cleared). Please respond with your Current Resume, Current Location and Current Company if you meet the requirements.
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Senior Clinical Data Manager
(US-New York) Coordinate in-house data management operations. Represent data management functionality at team meetings. Supervise clinical data specialists and data entry staff. Perform or oversee Case Report Form design. Perform or oversee database design and validation. Write data management plans and edit check specifications.
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Health and Safety Associate
(US-New York) Assist in implementing and training new hires in health and safety programs including Hazard Communication, Chemical Hygiene, Hazardous Waste Management, Spill Response, Respiratory Protection, Bloodborne Pathogen Exposure Control and Radiation Safety.
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Assistant Research Scientist
(US-New York) As part of a team the candidate will support our efforts for the HIV vaccine contract and will be involved in: Serological studies of animal sera immunized with different vaccine candidates. Immunological and biochemical characterization of vaccine candidates. Designing and performing purification processes for the recombinant proteins.
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Manager Regulatory Publishing
(US-New York) Evaluate, prepare, organize and publish documentation for electronic and paper submissions. Ensure documents are prepared in accordance with FDA, ICH guidelines & internal guidelines/SOPs. Manage junior/secondary/temporary publishers as needed.
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Associate Director Quality Assurance
(US-New York) Develop and execute plans to provide QA oversight of in-house and out sourced activities to meet project goals. Prepare CMC documentation to meet project goals. Serve as technical expert to direct Company programs in biologics and small molecules.
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Drug Safety Specialist
(US-New York) Review, evaluate, assess, and track serious adverse event (SAE) data received from the external vendor. Prepare and forward SAE related queries to the external vendor for clarification and/or additional information. Assist in the preparation of IND Safety Reports and Investigator Alert letters for submission to Regulatory and for notifications to Clinical Investigators.
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Associate Manufacturing Scientist - Cell Culture
(US-New York) Performs manufacturing processes including operation of bioreactors from the 5 L to the 1000 L scale in a cGMP environment; performing cell culture for preparation of bioreactor inoculum; performing routine bioreactor maintenance; performing initial purification/concentration steps and SOP writing and review.
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Manager / Senior Manager Formulation
(US-New York) Responsible for managing the development of new formulations for drugs in development. The scientific scope of the role ranges from initial pre-formulation through coordination with manufacturing of the initial commercial lot, and technical support for Manufacturing and Operations.
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Biostatistician
(US-New York) An opening for a biostatistics position to support statistical aspects of Phase II, III, and IV of pharmaceutical clinical trials. The candidate is required to have a Ph.D (MS) in Statistics with 1 to 9 years (4 to 12 years) of experience in clinical statistics.
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Medical Writer
(US-New York) Prepares clinical protocols and clinical study reports. Prepares materials supporting submission of INDs, NDAs, and ANDAs. Interfaces with contract Medical Writers to ensure timely delivery of high quality, on-budget medical writing deliverables.
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Clinical Project Manager / Associate Director
(US-New York) Recruitment of potential investigators, organization of meetings Identifies investigators and sites. Defines project task specifications together with medical director Interacts with our clients director of Operations and head of Biometrics to assemble study team. Reviews and approves Study Monitoring Plan.
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Patent Counsel
(US-New York) This newly created position will have a lead role in the development, protection and commercialization of the Company ntellectual property (IP) including patents, trademarks, trade secrets and copyrights. The position will report directly to the Company Vice-president and General Counsel.
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Clinical QA Manager
(US-New York) Develop, implement and track CQA programs Develop a quality plan for the Clinican and Regulatory groups. Support management of the internal QA audit process compliane to in house SOPs, systems and process documentation. Work with other disciplines to ensure training has been provided for specific job fundtions along with process improved initiatives.
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Virologist
(US-New York) Play a lead role in the discovery and development of novel small-molecule and antibody-based inhibitors of medically important viruses. Develop assays and methods to screen inhibitors of novel viral targets. Adapt methods to high-throughput screening.
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Clinical Trial Manager
(US-New York) Provides oversight management for CROs, consultants, and other vendors. Tracks and reports on the progress of assigned clinical trials. Assists in the development of protocols, synopses, and all study procedures documentation. Ensures that assigned studies are being conducted in accordance with the protocol, GCPs, FDA Regulations and departmental SOPs.
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Director / Sr. Director Clinical Research
(US-New York) Responsible for managing the direction, planning, execution and interpretation of trials/research and data collection activities. Establishes and approves scientific methods for design and implementation of clinical data collection systems and final reports.
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Formulation Manager
(US-New York) Responsible for managing the development of new formulations for drugs in development. The scientific scope of the role ranges from initial pre-formulation through coordination with manufacturing of the initial commercial lot, and technical support for Manufacturing and Operations.
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