DNAjobs.com is proud to feature the following jobs posted February 17 - 21 (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
Pharmaceutics Research Associate
(US-California) We currently have the following opportunity at our Thousand Oaks, CA facility. Research Associate III - Pharmaceutics Requirements: Bachelor's or Master's Degree in Life Sciences or a related field required. Typically 3-5 plus years relevant and increasingly complex laboratory experience also required. Job Summary: This position's primary responsibility is to develop biopharmaceutical formulations. The successful candidate must have solid grasp of biochemical and biophysical principles of protein activities and stability. Protein characterization skills are essential to succeed: highly proficient in chromatographic and electrophoretic analysis techniques and in-depth understanding of macromolecular spectroscopy and its applications. Experience and knowledge in biological mass spectroscopy, lyophilization and calorimetry are advantageous. Good troubleshooting skills for laboratory analytical instruments is helpful.
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Research Assistant
(US-Wisconsin) QUALIFIED CANDIDATE SHALL BE RESPONSIBLE FOR PREPARING AND MAINTAINING REAGENTS REQUIRED FOR INSTRUMENT QUALIFICATION AND VERIFICATION. CANDIDATE SHALL ALSO DESIGN AND PERFORM EXPERIMENTS INVOLVING REAL-TIME PCR AND APPLICATIONS THEREOF. CANDIDATE SHALL ALSO BE RESPONSIBLE FOR PREPARING AND MAINTAINING BASESTATION-RELATED CONSUMABLES THAT ARE SOLD TO EXISTING CUSTOMERS. CANDIDATE SHALL WORK COLLABORATIVELY WITH MOLECULAR BIOLOGY AND QUALITY SYSTEMS DEPARTMENTS IN ANALYZING SEQUENCING AND GENOTYPING GELS AND OTHER DATA GENERATED IN THE COURSE OF VALIDATING INSTRUMENTATION. GATHER DATA, PREPARE RESEARCH REPORTS, AND WRITE JOURNAL ARTICLES BASED ON RESEARCH. RESEARCH, DESIGN AND EXECUTE EXPERIMENTS OPTIMIZING REAL-TIME PCR INSTRUMENTATION AND OPTIMIZING TEST PROCEDURES & TEST REAGENTS RELATED TO SUCH DEVICES.
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Director Clinical Operations
(US-Massachusetts) The Director, Clinical Operations will be responsible for planning and executing clinical programs and managing clinical research resources including personnel and finances. The position requires the ability to work on problems/issues diverse in scope. Responsibilities: Establish clinical conduct infrastructure including but not limited to: documentation, clinical trial management systems, safety data collection and management and review/revise clinical research Standard Operating Procedures to ensure applicability. Establish and maintain Clinical Department budget: Report variances to management in a timely manner. Manage the execution of the clinical trials within the established infrastructure. Establish clinical research programs to meet the strategic objectives of the organization: Coordinate efforts to develop studies designed to meet the regulatory registration and/or marketing objectives. Define efforts and resources (financial, personnel and time) to meet program plans. Identify critical issues that impact the quality of the research program or impact the program resources (i.e., financial, personnel and time).
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Director Global Project Management
(US-Massachusetts) Director, Global Project Management Reports to: Executive Director, Global Project Management The ideal candidate will have a minimum of 7 years of development experience in a major pharmaceutical or biotechnology company, including having held positions in one of the discovery or development sciences. Prior experience managing multi-disciplinary project teams with demonstrated performance in successful IND and NDA submissions are also required. An advanced degree, either Masters or Ph.D. is desirable. Responsibilities: Manages global development projects. Responsible for overseeing assigned development projects to ensure meeting stated corporate goals and objectives. Tracks and manages project budgets. Facilitates information flow between team members and strives to identify and resolve issues arising on the project. Routinely reports progress to management. Key responsibilities include: Achievement of development project goals and milestones and integration of strategies across all disciplines involved with the project. Develop and implement specific communication tools that enhance information exchange and stimulate creative project interactions.
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Medical Writer
(US-Connecticut) Our client, a major pharmaceutical company in Stamford, CT is looking for a Medical Writer with the following qualifications: Experience: 3-5 Years Mandatory Industry Experience: Pharmaceutical Ideal Industry Experience: CRO Summary of Work to be Performed: Draft regulatory document templates (including clinical study report, clinical overview, and clinical summary templates) according to regulatory guidelines. Attend meetings and teleconferences with reviewers to understand and resolve comments and issues. Revise draft documents based on reviewer comments. Review regulatory documents to understand relevant concepts and focus. Review documents for consistency with American Medical Association format and style. Provide project management support by tracking timeline accomplishments for the identified stages of production. Assemble periodic status reports and presentations for management on regulatory template development. Primary Skills: Writing, organizational, project management, active listening, understanding of timelines. Secondary Skills: MS Office Suite, Gantt charting. Ideal Education Level - Certifications: Ph.D., Minimum Education Level: Masters Degree.
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Lab Technician
(US-New Jersey) Our client, a major pharmaceutical company in Cranbury, NJ is looking for a Lab Technician with the following qualifications: Experience: 1-3 Years Pharmaceutical. Required Knowledge of Machinery: pH-meter; balances; osmometer; tools for cell culturing. Primary Skills: Cell Culture, Cell Biology. Summary of Work to be Performed: Intensive assay-development / trouble-shooting is completed the assays. In October 2003 the Department of Molecular Pharmacology (Cranbury) acquired the 16-Channel Automated Patch Clamp System for $300,000.00 (PatchXpress 7000A /Axon Instruments, Inc.). This is a piece of cutting-edge technology that, for the first time, allows experimenters to directly record ion channel function with 10x the throughput of conventional electrophysiological measurements. For the intensive assay-development stage of the transfer it is necessary to have a technician to provide continuous cell culture support for the PhD staff operating the equipment. Assist with the assay transfer. Ideal Education Level/ Certifications: Bachelors Degree.
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Sr. Associate Scientist
(US-New Jersey) Our client, a major pharmaceutical company in Cranbury, NJ is looking for a Sr. Associate Scientist with the following qualifications: Experience 1-3 Years in Pharmaceutical. Primary Skills: Successful candidates should have a B.S. or M.S. in biology or related field and have 1 year experience working in a laboratory setting. Significant experience with carrying out biochemical and/or cell-based assay development, high-throughput screening, cell culture, and data management is required. Excellent proficiency with laboratory robotics systems is also required. Excellent communication and interpersonal skills are required. Secondary Skills: Experience with ion channel assays, enzyme assays, radioligand binding and functional assays for GPCRs would be an advantage. Experience with neuroscience or pain research would be an advantage. Required Knowledge of Machinery: standard laboratory robotics.
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VP, Strategic Partners Operating Unit
(US-Ohio) Our client, a highly respected international Clinical Research Organization, is interviewing qualified candidates for the VP of Strategic Partners Operating Unit. This high profile position will report directly to the President & COO of the company and will be responsible for all aspects of phase I-IV clinical trial activities with selected key sponsors. RESPONSIBILITIES: Overall responsibility for all financial (full P&L), management, marketing and sales for this unit. Develop and implement a strategic business plan and operating plans that will meet the needs of the clinical trials marketplace. Develop, train and mentor team members. Market/sell the operating unit's services QUALIFICATIONS: A Medical or PharmD degree is preferred. A PhD will be considered with extensive experience in the following requirements. In depth clinical development/clinical sciences and executive management experience. Must have strong knowledge/track record in marketing, ability to focus on strategice customers and projects, experience in a global setting and understanding of management responsibilities and financial fundamentals.
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Process Development Engineer
(US-New Jersey) Our Client, a biotechnology global leader in the processing of human bone, connective tissue and asceptic allograft tissue, has an immediate need for a Process Development Engineer. This newly formed position will report to the Sr. Director of Process Development. RESPONSIBILITIES AND DUTIES: *Design and implement manufacturing processes, instrumentation and equipment from laboratory through pilot plant and manufacturing scale *Provide engineering, design and process scale-up *Assist in equipment & systems problem solving, establish operating equipment specifications, new product scale-up, technology transfer and process specifications *Help determine future process and equipment optimum usage REQUIREMENTS AND QUALIFICATIONS: *BS Degree in Science or Engineering, Mechanical or Chemical *Process development experience with tissue, bone or allograft experience *2+ years industry experience in industrial process development, experimental process/equipment evaluation *Pilot plant experience preferred *QSR experience preferred.
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