Total Comp in the $165,000 range
Are you a Ph.D with at least 5 successful years selling in to the IVD (in vitro diagnostics market)?
Are you able to travel (in the midwest) up to 75-85%?
Do you live or can you relocate to Chicago?
This is an awesome position with a cutting-edge diagnostic and research company. Company is in need of a Ph.D Technical & Scientific Sales Manager.
Focus is on diagnostic solutions and tomorrow’s emerging technologies for molecular diagnostics, next generation ...
A. PRIMARY FUNCTION:
• Assures that new products are developed in line with the global registration requirements of targeted countries and obtains expedient registration of these products in a cost effective manner.
• Maintains registrations of existing products in compliance with applicable regulations.
B. MAJOR DUTIES AND RESPONSIBILITIES:
Develops regulatory strategies for development projects and manufacturing improvements, and analyzes risk vs. benefit in regulatory strategies to ensure ...
As the lead molecular biologist develop reagents to prepare clinical specimens for molecular amplification and analysis.
Assist in the development and validation of processes in various stages of development and product transfer into manufacturing.
Company is focused on achieving scientific excellence, and this is only achievable by employing people that are constantly striving to be the best. Offering an incredible starting salary to $70,000 as well as attractive employment packages, annual ...
Develop protein purification processes to be scaled up and transferred into manufacturing including evaluation of transferred processes, transfer of processes to manufacturing, harvest clarification, normal flow filtration, purification, tangential flow filtration, and product final formulation.
Apply your expertise in multiple facets of biologics development and manufacturing of Monoclonal Antibodies, Enzymes, Growth Factors, PEGylated Proteins and Cytokines derived from mammalian cell lines
As a key scientific leader create early clinical research strategies to drive the development of novel oncology therapeutics. Work with our clinics and laboratories to develop novel biomarkers, research tools and study designs derived from the safety, pharmacokinetic and pharmacodynamic data obtain in the early phase trials.
*** Determine the most efficient study designs, patient population and biomarkers to ensure the success of early clinical research
*** Conceptualize and implement ...
Seeking expertise in the identification and evaluation of gene expressed proteins or peptides acting as renal biomarkers to act as the primary contact and principal scientist and lead a small team in the design and development of mechanism of action studies for clinical trials and analyze and interpret data generated from MOA studies.
Additionally, shall lead collaborative efforts for in vitro cell based assays, stem cell differention, and biochemical assays design, development and data ...
Major pharmaceutical company seeks PhD and 3+ years experience in the following:
*** Designed and executed rodent in vivo experiments to evaluate the primary pharmacology and side effect profile of novel renal therapeutic compounds.
*** Expert knowledge in determination of Mechanism of Action, Pharmacokinetics & Pharmacodynamics, Animal handling, dosing, bleeding, subcutaneous, intraperitoneal, intradermal, and intravenous injections.
Candidate shall perform similar duties with the goal of ...
Job Responsibilities and Requirements: Responsibilities include rapid response to environmental incidents and disaster situations such as industrial accidents, spills, fires, hurricanes, and floods; performing multi-media environmental investigations at potential hazardous waste sites; and conducting oversight activities at hazardous waste removal sites. The ideal candidate will: Provide field support during emergency response situations, including air-monitoring and multi-media sampling. Provide ...
Data Analysis: Write SAS code for common statistical analyses. Understands and correctly uses validated SAS macros in the data analysis programs. Conducts thorough and detailed reviews of project documentation, program algorithms and analysis outputs. Interprets the analysis output clearly and effectively.
Identifies data analysis related issues and resolves promptly Study Preparation: Meets with CRA, R&D, Instrumentation scientists, department data collection programmers, and data entry to find ...
X-FACTOR: BS Chem, ChemE, Env., Health Biology…open. 5-10 years of Safety, Health, Environmental compliance. Experienced in safety protocols for compliance of pilot plant scale-up. Assure ISO and RC14001 compliance. Will consider fresh grads with co-op.
Y-FACTOR: Must be very “hands on” administrative type. Will teach and train across the board. Will manage project and programs but no employees. Very much a facilitator. Very detail-oriented. Also, very analytical by thought and nature.
Seeking scientist with molecular IVD expertise to optimize, scale up, and transfer nucleic acid based assays (DNA and RNA) from R&D to manufacturing for a novel IVD platform.
*** Optimize and Validate molecular assays targeting DNA and RNA
*** Perform Design Verification and Validation Studies
*** Scale up and Transfer molecular IVD assays from R&D into manufacturing
*** Maintain proper ISO and FDA QSR documentation and implementation
*** MS or PhD in relevant ...
Seeking 5+ years experience in biological manufacturing in a quality assurance function with track record designing, planning and conducting live training classes to assume responsibility for:
*** Course Development & Implementation
*** Policy Development & Execution
*** Metrics Development, recording and reporting
*** Administration and Coordination
*** Curriculum Development
*** Inspection Preparedness
Large company with diverse career path choice and generous benefits package ...
Focus on developing, revising, and proofing all reports related to the manufacturing of biologics to ensure compliance with applicable regulatory requirements. Establish priorities, deadlines and changes required for technical documents.
Requires a Bachelor’s degree in the life sciences and 2+ years of scientific writing experience.
Familiar with concept of design history files; familiar with documentation control system, such as Agile.
Would you like to join a company that has been voted top ...
Apr 2 -
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