DNAjobs.com is proud to feature the following jobs posted March 27 - April 3 (listed in chronological order). 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
Research Scientist
(US-California) Primary Responsibilities: Taking an active role in the development and growth of the company. Conductinganalyses and generating DNA sequence and multi-locus genotypes for services related to ancestry and paternity testing.In addition, we are seeking a candidate that has interest and research experience in the study and analysis of genetic variation and genetic identification at the individual, population and species levels.Duties: DNA Extraction, PCR amplification, RFLP, SNP, STR analyses, sequencing DNA of various species (mainly humans), managing the normal laboratory maintenance and operations, ordering supplies, creating and maintaining databases, assisting in the development and introduction of new techniques in the laboratory, and writing grant proposals topursue new lines of research. The candidate will also be expected to train and directly supervise laboratory technicians. Requirements: Candidate must have a PhD in a life science and experience with basic techniques and methodology ofmolecular biology, phylogenetic analysis, paternity analysis, population genetics and familiarity with public geneticdatabases.
(France-Champagne / Ardenne) A 2-year postdoctoral assistantship is currently available for a scientist possessing a PhD in a biochemistry or biology-related area. The successful candidate should have solid experience in recombinant DNA technology and especially in the area of recombinant protein production. The candidate will be a key actor in the development and use of a random mutagenesis strategy that will be applied to the improvement of the catalytic fitness of thermostable hemicellulases. The project will be performed within the framework of a collaboration involving two INRA teams, one based in Reims (Northeast France) and the other in Toulouse (Southwest France). During this two-year assistantship, the candidate will have access to a state of the art enzyme engineering facility that is housed within the Prof. Monsan’s Toulouse-based lab. Training in the areas of enzymology and HTS technologies will be given. Qualifications: a PhD in a biochemistry or biology-related area, good English fluency (or knowledge of French). Other skills: good oral communication skills and a willingness to travel (movement between the two labs) and work in different environments are essential qualities for this post.
(US) Our client maintains a repository of human biological samples and offers purified RNA, DNA, protein samples, tissue microarrays and disease specific protein expression databases. POSITION - Marketing Manager working in a staff position directly for an entrepreneurial CEO. Gaining great experience, then moving into a marketing line management position. Responsibility: As directed by CEO, will build a market-effective program on a project basis for client's life science products and services. Writing specification sheets, catalog copy, promotional materials, etc. REQUIREMENTS: Strong technical background (i.e.: minimum of Bachelor's cell biology--apoptosis, kinases, signal transduction, or histology or molecular biology) and must have 2+ years of related sales/marketing experience. MBA a plus. Can freely travel from Mid Atlantic headquarters thru the Northeast and to Western Europe. Looking for an overachiever with high capacity for work and desire to gain experience early in career, to move up the ranks. Someone that's fearless with a can do attitude. In addition to a solid understanding of related science issues, requires superior verbal, listening and writing skills.
(US-California-Silicon Valley/San Jose) This position manages a clinical group that supports clinical studies for new product development, modified existing products, marketing-claims, and products currently on the market. The manager coordinates activities of the clinical group, provides clinical guidance, and ensures compliance to company requirements and government regulations, including GCP. The essential functions and responsibilities are: perform management responsibilities (i.e. hiring, training, performance reviews, personnel and organizational development, budgeting, regular individual and department meetings); manage the external clinical studies group; establish priorities with management approval, provide adequate resources, support department personnel to meet deliverable expectations; review protocols, reports, and study documentation; develop appropriate department infrastructure to ensure project timeliness, adhere to regulatory requirements (i.e. procedures, training, capital, documentation archive, needed skill sets) and to company requirements; function as department liaison with other LifeScan departments in new and current product clinical studies; provide support and review for proposed studies external to the department (i.e. technical support, Marketing studies, customer requests, international studies); and ensure adherence to regulatory guidelines (FDA, ICH/GCP, and IVDD), LifeScan procedures, and J&J Corporate policies.
(US-Massachusetts-Boston) A leading research based pharmaceutical company with annual sales of $250 million plus, has an immediate opening for a Medical Director. This position will work closely with the Clinical Operations to design and prepare clinical trial protocols, data analysis and review plans for specific programs. Working with the Clinical Safety group the Medical Director will review and analyze safety data including adverse events and provide risk assessment. QUALIFICATIONS: Medical Degree and Board Eligible/ Board Certified in Pulmonology, Immunology, Pediatrics or a Respiratory therapeutic area. MUST HAVE Pulmonary experience. Prefer a candidate with 1-3 years of pharmaceutical industry experience but will consider a physician with strong academic/scientific experience and/or drug development experience as a clinical investigator. Able to work in a fast paced, multi-tasking office environment Competitive salary, bonus, stocks and relocation.
(US-New York-New York City) A well respected New York City based investment and strategic advisory group focused on the global pharmaceutical and biotechnology industry is seeking a highly motivated and entrepreneurially minded Biotech/Pharma Analyst. The candidate must have exceptional scientific grounding in cutting edge science and be interested in applying this perspective to financial and strategic analysis. The candidate must be well versed in one of the new scientific frontiers (i.e. immunology, genomics) and possess the maturity to judge the relative potential of competing technologies and therapeutic approaches in major disease areas (i.e. cancer, cardiovascular, anti-viral). The candidate must also have an understanding of key companies and industry trends in the pharma and biotech industries. Financial and strategic orientations are required as is an investment temperament. Excellent communication, interpersonal & writing skills are absolutely required. A PhD and/or MD and prior work experience in a biotech or large pharma company are preferred and an understanding of valuation methods is a plus.
(US-California-Orange County) Coordinate validation activities following the SDLC and compliant to corporate standards and regulatory requirements. Other core responsibilities are direct involvement in the creation of specifications (URS, FS, DS), writing of qualification test protocols (IQ, OQ, PQ), tractability matrices and respective validation reports. Assistance in the achievement of audit readiness for each facility within the scope of the program as well as coaching of the local site teams in validation. Intense cooperation with technical teams in the facilities and the global implementation team is expected as well as travel (up to 50%). Qualifications Project management and leadership Minimum of 3 years experience in Validation in the Pharmaceutical/Biotechnology Industry. Strong knowledge of validation with focus on PQ, OQ and IQ Validation protocol and test case creation (PQ, OQ, IQ). Strategic view and understanding of validation. Understanding of risk based validation Business analysis skills. Strong familiarity with LIMS as a concept. Familiarity with SQL LIMS as a product. Solid knowledge of the cGMPs (21 CFR 11, 210/211, 820 and 606) as well as GAMP Experience with creation and utilization of Specifications (URS, FS, DS).
(US-Indiana-Indianapolis) Job Responsibilities/Requirements include: Supporting remediation efforts by providing validation/technical writing support. Write and/or revise validation documentation for lab and manufacturing systems within a manufacturing plant. Examples of systems include: chromatography, PLCs, and IT systems. Diverse system experience is a plus. Must have knowledge of the validation lifecycle and 21 CFR Part 11. Should have 2-3 years of experience validating systems in the manufacturing area of a pharmaceutical company. Should be comfortable working closely with engineers, gathering technical information and developing documentation. Must be a self-starter and work independently. Must be proactive and meet strict deadlines and tasks assigned. A person with strong writing skills and solid validation knowledge is a good candidate. Written and verbal communication skills must be excellent.
(Bangalore - India) 1) Project Lead- Pharmaco-Informatics: Ph.D in Pharmaceutical Chemistry/ Molecular Pharmacology with 3-4 yrs experience in an established industry or scientific institution. People management skills are essential. 2) Trainee Scientists- Pharmaco-Informatics: Fresh Ph.Ds/M.Pharm in Pharmaceutical Chemistry/Molecular Pharmacology. 3) Trainee Analyst, Pharmaco-Informatics: Fresh B. Pharm with excellent academic record. 4) Trainee Scientists,Chemoinfomatics/Bioinfomatics: Fresh M.Sc. in Organic/ Medical/ General Chemistry or M.Sc. with specialization in Molecular Biology/ Biochemistry. 5) IT Analysts: B.E/ B.Tech/ MCA/ MSc (Comp.Sci.) with good exposure to any of the following: - Progamming in C++ & JAVA, and Rational tools - Expertise in X-Windows / Motif, Linux GTK, OpenGL, 2D-3D graphics - Application development in multi-tier architecture, object oriented technologies, Oracle 8i/ 9i.
(US-California-San Francisco) Sales Manager - Bay Area Proteomics, Gene Expression, Molecular Biology, Drug Discovery A world leader in the Proteomics & Molecular Biology fields, with offices in Japan, Europe and the United States, is searching for a Regional Sales Manager to cover clients in the San Francisco Bay Area, with occasional travel to Southern California. The firm is a PROFITABLE biotechnology company that provides proprietary technology tools to researchers in the Pharmaceutical, Biotech, and academic markets for drug discovery. The firm is introducing new product lines that instantly makes this company the largest supplier of such products in the world. The firm is also THE leading provider of Contract Research Services within their technical discipline. Responsibilities: Maintain and continue development of relationships with existing clients. Identify and initiate new business opportunities. Identify key decision-makers within potential clients and coordinate client visits with appropriate personnel from the firm. Identify client's future needs and make new product recommendations to firm. Responsible for initial contact with prospective clients, through eventual successful conclusion of the sales process.
(India - Delhi, Mumbai, Calcutta, Chennai and Lucknow) Role: Responsible for achieving targets, expanding business by seeking new opportunities including large institutional business. You will lead a large team and establish systems & processes. You will function virtually like an SBU head with profit responsibility. You will build rapport with government & influential members of the society. Profile: You should have strong sales instincts, man-management skills, and organizational abilities with emphasis on systems. You should have excellent communication skills. Experience: A 5-7 years experience in sales (Pharma or FMCG) with at least 2-3 years at handling large teams. Excellent sales record. Qualifications: Graduate/ MBA.
(Australia-New South Wales-Sydney) The Molecular Biology Fellow must have a PhD (or equivalent) with an outstanding academic record and experience in cDNA library screening, cDNA library construction and experience working with bacteriophage (for example phage display or phage library screening). Desirable criteria would be bacterial protein expression and purification, experience working with T7 bacteriophage, phage display and ligand receptor binding. Salary: $55,640 per annum Grants are provided towards travel and removal. Positions are initially for one year with a possible extension of six months. There is a housing office to help find accommodation. The project will be within the Institute of Biology and Chemistry, which incorporates both the Departments of Chemistry and Biological Sciences and the Australian Proteome Analysis Facility (APAF), Macquarie University Centre for Analytical Biotechnology (MUCAB). We have impressive infrastructure for this project including NMR (Bruker DRX600 and DPX400), mass spectrometry (LC-ESI, ESI- TOF, MALDI-TOF, MALDI-TOF/TOF, GCMS), chromatography (HPLC; Waters, Shimadzu, FPLC; Äkta, Smart, BioCad), electrophoresis (11, 17 and 24 cm 2D format gel systems, image analysis, electroblotting, MS analysis and bioinformatics) and BiaCore.
(Australia-New South Wales-Sydney) The Chemistry Fellow must have a PhD (or equivalent) with an outstanding academic record and experience in organic synthesis. Desirable criteria would be experience specifically in natural products chemistry, structure elucidation (NMR spectroscopy), chromatography (HPLC), biotinylation and linker design/synthesis and working with water soluble compounds. Grants are provided towards travel and removal. Positions are initially for one year with a possible extension of six months. There is a housing office to help find accommodation. The project will be within the Institute of Biology and Chemistry, which incorporates both the Departments of Chemistry and Biological Sciences and the Australian Proteome Analysis Facility (APAF), Macquarie University Centre for Analytical Biotechnology (MUCAB). We have impressive infrastructure for this project including NMR (Bruker DRX600 and DPX400), mass spectrometry (LC-ESI, ESI- TOF, MALDI-TOF, MALDI-TOF/TOF, GCMS), chromatography (HPLC; Waters, Shimadzu, FPLC; Äkta, Smart, BioCad), electrophoresis (11, 17 and 24 cm 2D format gel systems, image analysis, electroblotting, MS analysis and bioinformatics) and BiaCore.
