DNAjobs.com is proud to feature the following jobs posted October 15 - 22. 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
Marketing Biologicals
(India-Delhi) Person with biological science background, and flair for marketing who is willing to travel. Company Profile: Primarily engaged in marketing of Equipments / Consumables for use in bio research and healthcare.
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Bioinformatics Research
(India-Andra Pradesh-Hyderabad) To fuel the growth of our Informatics Division based in Hyderabad, we are looking for Postgraduates with knowledge in the areas of Chemistry, Pharmacy and Microbiology. Candidates working in pharmaceutical or biotech companies with experience in drug discovery and development, bio and cheminformatics will be preferred.
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Project Manager
(Germany-Frankfurt) Responsible for the successful implementation of InfoPro software at the client site. Work directly with clients to ensure project delivery meets clients expectations. Coordinate Business and Support analyst activities to execute project plan. Requirements/Qualifications: Successful track record of managing of one or more pharmaceutical system implementations.
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Senior Validation Analyst
(India-Karnataka-Bangalore) Qualifications / Technical Skill Set: Preferably in possession of an engineering degree. Has to be fully aware of SDLC process. Effective management of a 10+ staff of developers, QA and analysts. Must be able to manage a team effectively and independently. Must be aware of different types of test scripts and test strategies.
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Department Head - Development Quality Control
(US-California) In charge of managing a department responsible for release and stability testing of both small molecule and Biologic drug substances and drug products used in early phase clinical development projects. Department also supports process and formulation development. Reports to the Director of Analytical Development.
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Department Head - Small Molecule Analytical Chemistry
(US-California) In charge of managing a department responsible for development, qualification/validation and application of analytical methods used to characterize small molecule drug substance and drug products used in early phase clinical development projects. Department also supports process and formulation development and transfer of methods to different sites.
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Project Leader
(India-Karnataka-Bangalore) Qualifications / Technical Skill Set: Preferably in possession of an engineering degree. Adequate experience and knowledge in SDLC processes, QA, preferably CMM/ISO procedures and would be required to perform code walk through to ensure compliance to coding standards.
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Developers
(India-Karnataka-Bangalore) Qualifications / Technical Skill Set: Hands on experience in Oracle, D2K and other tools. Thorough knowledge of SQL, PL/SQL and Forms and a fair degree of competence in Oracle 8i and Reports. Exposure to Web-related tools and QA methodologies is desirable though not essential.
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Biopharmaceutical Market Research Manager
(US-Florida) Develop and execute marketing research plans for the United States. Develop product design to address primary research needs. Develop product pipeline forecasts. Develop action plans and recommendations based on results of marketing research. Work closely with internal clients including Sales, Marketing, Business Development, etc. to identify marketing needs.
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Clinical Research Associate
(Canada) The clinical research associate monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols. Review regulatory documents as required and prepare site visit reports. Responsible for multiple projects and must work both independently and in a team environment.
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Senior QC Analyst
(India-Karnataka-Bangalore) Qualifications / Technical Skill Set: Preferably in possession of an engineering degree. 3 to 5 years of experience. Has to be fully aware of SDLC process. Must be able to manage a team effectively and independently. Hands on and thorough experience in Win Runner.
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Biostatistician
(India-Andra Pradesh-Hyderabad) M.Sc in Biostatistics with 3-5 years of experience. Performance areas would be inputs for generation of protocols, management and evaluation of data and writing statistical reports.
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Facility Trainer
(US-Maryland-Montgomery County) SoBran, Inc., a rapidly growing biomedical laboratory services company, has a full-time opening for an experienced Trainer at one of the NIH, Bethesda, MD sites. Qualified applicants will have a High School diploma or equivalent. Must be AALAS certified preferably at the LATG level.
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Group Leader - Analytical Chemistry
(India-Andra Pradesh-Hyderabad) M.Pharm. / M.Sc / Ph.D in Analytical Chemistry with 3-5 years experience in Bioanalytical Research.
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Staff Nurses
(India-Andra Pradesh-Hyderabad) B.Sc Nursing with experience of working in the ICU and capable of handling medical exigencies. The responsibility would also include providing nursing care to the volunteers and blood collection.
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Sales Representative (Inside)
(US-California-Los Angeles) This position will report to the Director, Product Services and will be responsible for selling company products and services by contacting prospective and established customers. The Sales Representative will follow up on leads and establish close customer contacts to promote company products to select accounts as designated by Sales Management.
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Research on Algorithms and Architectures for Computational Biochemistry
(US-New York) Extraordinarily gifted computer scientists, systems architects, electrical engineers and systems software professionals are sought to join a rapidly growing New York–based research group pursuing an ambitious, long-term project aimed at achieving major scientific advances in the field of biochemistry and fundamentally transforming the process of drug discovery.
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Senior Research Associate / Research Associate (SRA / RA)
(India-Andra Pradesh-Hyderabad) M.Pharm with 4-5 yrs experience in Bioequivalence. The job profile would include: Writing and reviewing of SOPs Protocol Preparation. Monitoring GMP in the clinic. Review of clinical reports. Interact with QA department during the studies. Knowledge of implementation of GLP and regulatory guidelines.
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