Biotech Startup Jobs

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The Senior Environmental Engineer will ensure compliance with environmental regulations and permits. Other responsibilities include, but are not limited to: Development, modification, and implementation of environmental permits, plans, and company procedures to ensure compliance with environmental regulations and corporate programs, procedures, policies, and manuals. Leading internal departments...
Oversees all aspects of management of laboratory operations within the different functional groups of the GMP, GCL, Vaccines & Biologics or Bio-Analytical laboratories. Ensures productivity, efficiency and quality of the work are maintained and financial objectives of the business are achieved. Oversees the development and implementation of laboratory systems and processes. Ensures client delivera...
GENERAL: Participate in and manage both stability and sterility activities in the stability program for PharMEDium?s services. RESPONSIBILITIES: Assist in the design and acceptance of method validation protocols preparation and execution of stability testing protocols. Manage new product evaluations based on current stability data. Identify potential areas where current stability data and lite...
Novum is looking for an individual that possess strong management skills, good clinical practices, experience with FDA regulations, research studies and other regulatory standards. Position Summary Day to day staff management and clinic conduct of Phase I investigations. Responsibilities Coordinate all clinic activities and support service, to ensure coverage; for example, clinic set-up, scree...
Hays is currently recruiting for a Project Manager for our global pharmaceutical client located in Northern NJ. This hands-on, process driven Project Manager position is a 6 month contract job. This position is an excellent opportunity to leverage your Drug Development and Regulatory Filing experience in a tangible project-based setting. This position will be responsible for hands-on daily projec...
Global Stability Operations works closely with each Hospira plant to ensure all stability commitments are met, including the annual placement of each Hospira product required on stability, reconciliation of special stability commitments, compilation of reports used by Regulatory Affairs for use in submissions and annual updates. The gropu controls the Stability database where all stability data is...
As part of the iCAD/Xoft Clinical Affairs team, the Clinical Affairs Project Manager will be responsible for the coordination of all activities associated with the conduct of multiple clinical trials (develops study protocols, CRFs; supervises study tasks and mentors other CRAs; assists in the generation and oversight of trial budgets and contracts; and communicates trial status to management). In...
Assist in monitoring and collecting data from sponsor initiated clinical study. RESPONSIBILITIES: Travel to clinical research sites to collect clinical data for publication Check the data for compliance with study/site protocol, consistency and quality assurance Post-process, analyze the collected data using various software tools Document and report the analysis results Work with Investigat...
If you are a confident and highly motivated individual looking for a great sales opportunity with uncapped earnings and growth potential, join our team at MedSupply Partners! MedSupply Partners is a nationwide distribution company that specializes in providing high quality laboratory equipment, reagents and consumables to academic research laboratories and biotechnology/pharmaceutical companies. ...
To maintain and coordinate Quality Systems related documents namely deviation reports, change controls and product complaints for compliance with cGMP and company procedures with minimal supervision. To review and write cGMP procedures under supervision. To process changes in analytical methods, test specifications and batch records. To issue effective documents including procedures, forms, report...
RMC is seeking an environmental protection specialist with a bachelor’s degree and 7 years experience or a master’s degree and 3 years experience with environmental impact assessment and NEPA (AICP certification is a plus). The candidate should have background in transportation planning for transit project development and/or city/urban planning. Must have a working knowledge of NEPA, NHPA/Section ...
At St. Jude Medical every one of us plays a role in our collective ability to save and improve lives. As an organization, we want to continue to grow and lead our industry in changing the way the world views the treatment of expensive, epidemic diseases. By seeing things from a different perspective, using our imagination, leading with character, and working with passion, we all have a role to pla...
The scientist will be part of a team effort to provide cell banking services to the Client, other R&D customers, Client Supply Chain and other clinical and commercial manufacturing sites. The scientist will perform cell culture according to Standard Operating Procedures using Good Manufacturing Practices. Primary responsibilities will be: Culture and cryopreservation of a variety of cell lines ...
Follows current GMP requirements and complies with company safety policies. Participates in repair and maintenance of lab equipment and laboratory housekeeping (disinfection and cleaning). Initiate, document, and perform microbiological analysis on received test samples (including raw materials, bulk, final product, stability, water) as per USP, in-house, or customer methods. Evaluates and record...
United Therapeutics Corporation is a biotechnology company focused on the development and commercialization of unique products to address the unmet medical needs of patients with chronic and life-threatening conditions. We have four approved products on the market today and we are not stopping there! From the United States to Europe to the Asia Pacific, we are proud of our multicultural business e...
NPA Coatings Inc., a manufacturer of liquid coatings and pre-treatment chemicals is currently seeking a Chemist to join our Liquid Division supporting the Cleveland production operations. The Chemist position is responsible for testing, formulating, analyzing and experimenting with raw and in process material. The Chemist interacts with others within the department to support existing products whi...
United Therapeutics Corporation is a biotechnology company focused on the development and commercialization of unique products to address the unmet medical needs of patients with chronic and life-threatening conditions. We have four approved products on the market today and we are not stopping there! From the United States to Europe to the Asia Pacific, we are proud of our multicultural business e...
This pharmaceutical company is known as a human health care (hhc) company seeking innovative solutions in disease prevention, treatment and care for the health and well-being of people worldwide. They use their talents to explore new therapeutic approaches that help address two key goals: meeting the medical needs of patients and their families, and improving their quality of life. Job Descriptio...
We are looking for Validation Engineer for the leading biotech company is South San Francisco. Below is the job description. Interested candidates, please submit your resume to ***** or call (510) 353 1700 Ext. 231 to discuss further about this position. Job Description: Job Title Systems Engineer - Verification and Validation You will work in collaboration with R&D, Marketing and P...
Controls Engineer needed for Automotive Tier 1 Supplier in Northern Kentucky/Greater Cincinnati. You will maintain machine, robot and equipment prints and resolve major programming issues. You should have a strong PLC troubleshooting and programming background within heavy industry. Must be open to 1st or 2nd shift. Responsibilities for the Controls Engineer Debug and implement process improveme...

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