The following career opportunities were posted this week at DNAjobs.com. 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
Senior Research Positions
(China) Senior Research Positions Medgenn Inc., Yantai, Shandong, China Yantai Medgenn is one of the leading biotech companies in China. With one drug already in clinical trial phase III, the company is more than ever committed to promote excellence in drug research and development. In the midst of a significant expansion of the R&D group, we invite outstanding scientists to apply for multiple senior research positions. Though not limited to, we are particularly interested in people with experience in one or more of the following fields: 1) protein expression in eukaryotic cells; 2) pharmaceutics; 3) protein or chemical drug design. Applicants with industrial experiences and with experiences either on animal models for drug screening or clinical trial designing are strongly encouraged to apply. Medgenn offers competitive salaries, good stock incentive plan, subsidized housing and other compensation benefits.
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Senior R&D Scientist - Cell Culture
(US) Ideal candidate will have a PhD or MS ( with 5+years relevant experience) in Cell Biology, Molecular Biology, biology or other life science. Experience in the culture of mammalian cells and a broad knowledge of mammalian cell biology is required. Experience desired in media development for cell lines producing recombinant proteins and/or engineering of these types of cell lines, the cultureof CHO/NSO cells and antibody production. Knowledge of , and the ability to exploit the mechanisms underlying cell functions such as attachment, proliferation, and cellular metabolism is highly desired. You must have demonstrated experiencein independent experimental design (DOE),data analysis, andexcelllentwritten and oral communication skills. Excellent team and leadership skills. Good computer skills includimng MS Office.
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cGMP Protein Purification Manager
(US) You will have responsibility for our protein purification activities, employee development and training,and quality systems. 10+ years experience in protein purification (downstream processing experience desirable.) CGMP manufacturing experience desirable. Direct experience in the manufacture of therapeutic proteins for clinical use. Experience with antibodies, protein folding, and inclusion body work helpful. Mammalian cell culture or bacterial fermentation experience desirable. Prior employee supervisory experience or managerial responsibility required.
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R&D Scientist
(US) PhD in chemistry with demonstrated skills in Inorganic synthesis. Interest in research & development of new products & process improvements of existing products for catalog & custom requests is required. Experience with ultra-pure inorganics and metals for high tech uses a plus. Must be self-motivated, flexible,team player. Good communication and interpersonal skills. Small companybusinessknowledge and experience is desirable. Interest in superbvision of other chemists a plus.
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Process Development Scientist
(US-California) Our client, a major pharmaceutical company in Freemont, CA is looking for a Process Development Scientist with the following qualifications: Incubant will work at a Biopharmaceutical company in the East Bay to be part of a joint research/development team doing downstream process development work on a new recombinant biologic. Must have a BS/MS/PhD in Biochemistry, Biological Science, or Chemical Engineering (with a biotech background) with 5 years+ exp. in process/product development, 3 years exp. with protein purification using analytical techniques (HPLC, LC), and scale-up. Must have an emphasis in preparative chromatographic skills, HPLC, and electrophoretic anaytical techniques. Must also have extensive experience with cGMP, strong analytical and organizational skills, excellent written/oral communication, collaborative and interpersonal skills.
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Healthcare - Pharmacist
(US-Illinois) Our client, a major pharmaceutical company in Lake County, IL is looking for a Healthcare - Pharmacist with the following qualifications: Reviews prescriptions issued by Physician, or other authorized prescriber to assure accuracy and determine formulas and ingredients needed. Compounds medications, using standard formulas and processes such as weighing, measuring, and mixing ingredients. Directs pharmacy workers engaged in mixing, packaging, and labeling pharmaceuticals. Answers questions and provides information to pharmacy customers on drug interactions, side effects, dosage and storage of pharmaceuticals. Maintains established procedures concerning quality assurance, security of controlled substances, and disposal of hazardous waste drugs. Enters data such as patient name, prescribed medication and cost, to maintain pharmacy files, charge system, and inventory. Assays medications to determine identity, purity, and strength.
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Clinical Statistician II - A
(US-Illinois) Our client, a major pharmaceutical company in Lake County, IL is looking for a Clinical Statistician II - A with the following qualifications: REQUIRES 0-3 YEARS EXPERIENCE Provide in-depth statistical expertise in the areas of; experiment, protocol, case report form design, data base structure, and analysis plan; collaborate with the medical groups to complete joint scientific reports and FDA overviews, including review of such reports to ensure accuracy and clarity. May also contribute to the decision for optimal study design and contribute to the proper use of statistical methodologies for a study. Must have clinical research experience. MS Preferred (PHD). MS in statistics or biostatistics required. Must have 0-2 years of experience.
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Post Doctoral Research Scientist – Genetics of Coronary Heart Disease
(US-New York) The “Laboratory of Biochemical Genetics and Metabolism” at Rockefeller University is looking for a research scientist. The project combines studies in both human and mouse genetics to unravel the genetic basis of coronary heart disease. Two project components, the study of the genetics of heart disease risk factors in a Micronesian Island population and the development of mouse models of atherosclerosis to identify modifier loci, have advanced to the point where they are ready for this analysis. The position offers an enterprising individual the opportunity to make a breakthrough in the field and achieve appropriate recognition. The selected scientist will work with pioneers in the field of genetics of heart disease, obesity, diabetes, and hypertension. Location: The Laboratory is on Manhattan’s Upper East Side adjacent to Sloan Kettering Cancer Research Center and Memorial Hospital as well as the Cornell-Weill Medical School and New York Hospital.
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Post Doctoral Research Scientist – Mouse Models of Diabetic Complications
(US-New York) The “Laboratory of Biochemical Genetics and Metabolism” at Rockefeller University is looking for a research scientist. The project is focused on making a mouse model in which diabetes greatly worsens macro vascular disease. The Laboratory is breeding mouse models of atherosclerosis, such as the LDRL receptor knockout mouse, with mouse models of hyperglycemia, insulin resistance or both and evaluating effects on vessel wall biology and atherosclerotic lesion progression. The position offers an enterprising individual the opportunity to make a breakthrough in the field and achieve appropriate recognition. The selected scientist will work with pioneers in the field of genetics, heart disease, obesity, diabetes, and hypertension. Location: The Laboratory is on Manhattan’s Upper East Side adjacent to Sloan Kettering Cancer Research Center and Memorial Hospital as well as the Cornell-Weill Medical School and New York Hospital.
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Investigator/Analytical/Bioanalytical
(US-Massachusetts) Manage and lead a functionally oriented team focused on analytical method development and high throughput characterization of parallel synthesis products. RESPONSIBILITIES: 1)Manage a 13 member team (of BS, MS, PhDs) that provides method development capabilities to synthetic chemistry and maintains a HTP characterization operation. 2) Assure a high level of productivity and maintain the team on the cutting edge of high throughput characterization, responding to changing needs of external collaborations and analytical methods that become available. 3) Interact closely with peers from synthetic chemistry and parallel synthesis operations to assure an efficient process and productive work flow. Requirements: EXPERIENCE: PhD, ideally with a Post-Doc and at least 7-10 years industry experience or equivalent. A strong background in either separation science or mass spectroscopy, ideally with a PhD obtained in a recognized lab that specializes in either one PLUS Experience with quality control/characterization of small organic molecules.
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Analytical Chemist
(US-Massachusetts) Keys: Supervisory experience, small molecules, method development, Mass Spec. If you possess these attributes, you should read on! Responsibilities: An opportunity currently exists to manage and lead a team of scientists (10-15) focused on analytical method development and HT characterization of synthesis products. You and your group will work closely with peers from synthetic chemistry and parallel synthesis operations to assure an efficient process and productive work flow. Education: PhD with Post-Doc. Requirements: You should have 10+ years of biotech/pharma industry experience. A strong background in separation science or mass spectroscopy combined with quality control/characterization of small organic molecules.
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Research Scientist-Formulations
(US-Massachusetts) Develop and characterize formulations to support small molecule drug discovery and development programs. The position requires hands on laboratory work. Job Responsibilities: Establish a formulation development and testing lab. Develop prototypes of formulations (solid and liquid dosage forms for injection and oral dosing). Characterize new drug substances and formulations with respect to relevant thermal, solid state, solubility, and stability properties. Hands on operation and maintenance of analytical instruments. Effectively transfer research formulations developed in the lab to the manufacturing facilities. Assist with defining QC specifications / audits / generation of documents for regulatory agencies. Education/Experience: Ph.D. with a minimum of 3 years industry experience developing formulations for injection and oral dosing (capsule and tablet) of small molecules.
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Associate Bioinformatics Scientist
(US-Florida) A research institute located in Florida is seeking an Associate Bioinformatics Scientist for their Bioinformatics Services & Research IT division. Primary Responsibilities: Will work closely with researchers from various departments who are involved in molecular biology and biotechnology research with an emphasis on translational science. Will work in a UNIX environment with all the standard biotechnology software. Assist in data mining and analysis using advance software tools. Assist in algorithm/software development for various molecular biology problem resolution. Requirements: PhD in Bioinformatics, Molecular Biology, Biochemistry or related area with one (1) year experience in Computational Biology or Bioinformatics field. Must be proficient in the analysis of micro array data (Affymetrix), the related algorithms, statistical analysis and biological interpretation of data.
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Associate Medical Director
(US-Massachusetts) A leading contract research organization in the Boston area has an immediate opening for an Associate Medical Director to work closely with clients to develop strategies for the use of imaging in clinical trials. The position will provide expertise on imaging related projects that are used to evaluate the safety or efficiency of a drug or medical device. REQUIREMENTS: PhD or MD with specialty training in imaging (radiology); would consider cardiologist, oncologist or neurologist if the candidate has a STRONG imaging background. 3 years of clinical and/or clinical trial experience. Prior industry experience preferred. Good working knowledge of medical terminology and standard medical practice. Excellent written and verbal communication skills.
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Director/Exploratory Research
(US-Massachusetts-Boston) The successful candidate will lead the Research team in formulating strategic decisions related to new technologies, new product development opportunities, design and assessment of proof-of-principle experiments, and technological risk assessment for new product concepts. The ideal candidate will have a Ph.D. in cell biology, molecular biology, or related discipline and at least 5 years post doctoral or industry research experience with a proven ability to manage multiple research projects and provide sound scientific judgment. Biotechnology industrial experience is a plus. The successful candidate will possess a broad working knowledge of, and interest in, the biomedical sciences as well as a demonstrated skill in moving therapeutic concepts to preclinical candidates using highly focused proof-of-principle studies.
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Director of Business Development
(US-Massachusetts) Reporting: The Director, Business Development will report to the Vice President, Business Development. Essential Job Function: To represent the COMPANY in interactions with pharmaceutical companies, biotechnology firms and academic organizations in pursuing opportunities for in-licensing and out-licensing products or technologies for development and commercialization. Individual Responsibilities: Collaborate in the development and execution of a comprehensive business development program to identify potential business partners and promising alliances. Utilize a strong knowledge of the pharmaceutical and biotechnology industries to identify, investigate and assess corporate partnering opportunities, and initiate discussions pertaining to both in-licensing and out-licensing opportunities. Foster relationships with pharmaceutical companies, biotech companies and academic organizations by providing relevant information to interested parties, arranging meetings and facilitating technical discussions between company representatives.
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Manager Regulatory Affairs, Labeling and Promotion
(US) It may be cold here in the Northeast but this Company is HOT! Do not wait to respond to this position. What will the qualified candidate do: You will be responsible for the management of regulatory activities in the support of external commercial communications, labeling development and labeling maintenance. You will represent regulatory in cross-functional teams that review and/or approve promotional materials, sales training materials and press materials. You will represent regulatory in cross-functional teams that develop draft labeling for regulatory authority review and approval. You will be the liaison with regulatory authorities and other functional teams within the Company in labeling and promotions. What is your education/experience? BS degree and minimum 2 years experience in regulatory promotional review or labeling.
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Manager Regulatory Affairs
(US) Have you experience in IND’s and BLA’s? If so, you will want to learn more about this opportunity! What will the qualified candidate do? Represent RA on all relevant project teams. Responsible for the development and implementation of RA strategy for assigned projects and programs. Responsible as the primary contact for all communications with the regulatory agencies relevant to assigned projects or programs. Responsible for coordinating all aspects of regulatory submissions relevant to assigned projects or programs. May supervise regulatory associates. Prepare written and oral presentations of Regulatory plans to project teams and Senior Management. Participate in industry associations. What is your education/experience? BS/MS degree and a minimum of 3 years experience. Extensive knowledge of US regulations and some international regulatory experience preferred.
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