Biotech Jobs

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Requirements: Experience in statistical analysis, machine learning, and clustering algorithms, and software development Experience with predictive modeling is preferred – multivariate regression, logistic regression, and time series analysis Some experience in optimization and stochastic processes Experience with Matlab, R, or Weka Strong plus: 1+ year’s developing software in java, python, C+, or...

Job Description: Job Details: Under general supervision, this position will perform routine processes relating to templates testing procedures into Corp electronis systems in support of the data acquisition integration initiative. This position will be responsible for one or more of the following activities: - Performing quality checks of template information to confirm accuracy, running scenarios...

Job Description: This Sr Associate GRAAS Operations Position Features: ? E ? E ? E ? Great Pay to $0K Immediate need for sr associate graas operations seeking e, e and e. E, e and e will be keys to success in this prestigious organization. Will be responsible for e, e and e for Biotechnology/Pharmaceuticals company. Great benefits. Apply for this great position as a sr associate graas operations t...

Research Technician in Gene Regulation Job Description: The selected candidate will split their time between research activities and laboratory management. Perform plasmid cloning, PCR, manipulation of animal virus vectors, transfection, and cell/mouse based assays. Produce reliable, precise, and carefully recorded data to support our scientific investigations. Interpret and present findings to co...

The ideal candidate is a clinical laboratory professional with extensive experience in all aspects of laboratory operations and with the development and commercialization of molecular assays, immunoassays, medical devices and diagnostics. Due to the strategic nature of this role, effective communication skills are a MUST. The candidate must be able to convey the business implications to executives...

Akcea Therapeutics, Inc., a subsidiary of Isis Pharmaceuticals, Inc., is focused on realizing the transformative potential of the leading RNA-targeted technology for patients with complex dyslipidemias. Based in Cambridge, MA, Akcea is developing and commercializing six drugs discovered and initiated by Isis for its Lipid Franchise, anchored by ISIS-APOCIIIRx, currently in Phase 3 development. Akc...

Our client on the Peninsula is looking for a Research Associate II to add to their team! Duties: The Research Associate II will perform R&D activities as part of a highly collaborative team, sometimes on complex problems. Conduct research and development activities with limited supervision and direction from supervisor. Conceptualize appropriate controls and procedures designed to foresee potentia...

Job Description: Job Details: The position will involve assay support and evaluation of stability for protein therapeutic formulation candidates. Desired experience includes size exclusion HPLC, cation-exchange HPLC and knowledge of particle analysis techniques such as HIAC and MFI (Micro Fluidics Imaging). A knowledge of speadsheet programs such as Excel and chromatography software such as Chrome...

Collaborative is seeking a Regulatory Affairs Associate for long term contract position with large pharmaceutical company located in North Chicago, IL Position Description: The candidate will be the primary point of contact to provide change control execution and expertise in the context of CFR 820 Design Controls. The candidate will be responsible for creation/remediation, maintenance, accuracy a...

Collaborative is seeking a Research Associate for long term contract position with large pharmaceutical company located in Santa Clara, CA Position Description: Designs and conducts experiments, summarizes data, interprets results and draws conclusions. Prepares summary reports based on test results and conclusions. Proactively presents scientific observations to others. Evaluates data using analy...

Job description Serve as an Hazard Assessment and Communication Specialist. Critical role in ensuring company supports customer safety goals, and complies with global regulations governing hazard communication, and supports innovation and business goals. Primary tasks Conducting chemical hazard assessments Manage and maintain hazard assessments in a centralized database Update hazard assessment cr...

TechData Service is interested to talk to you about open contract positions with our top pharmaceutical clients. Currently, we have openings for home-based Sr CRA (Senior Clinical Research Associate),Process Documentation Writer, (Cambridge, MA), Project Manager- Scientific, Regulatory Affairs Manager, Standard Operating Procedure Coordinator,(Lexington, MA), home-based Biostatistician – Phase I,...

Job ID: 38317 Position Description: Clean Harbors is the leading provider of environmental, energy and industrial services throughout North America. The Company serves a diverse customer base, including a majority of the Fortune 500 companies, thousands of smaller private entities and numerous federal, state, provincial and local governmental agencies. Through its Safety-Kleen subsidiary, Clean Ha...

Senior Regulatory CMC Specialist Job Summary Leading global pharma organisation is seeking a Senior Regulatory CMC specialist, who has a proven track record of Regulatory Strategy and Regulatory Submissions process (Regulatory/Submissions/CMC) to join the Regulatory Affairs team. This is a 12 month contract based out of Key Activities: Provides strategic regulatory input and regulatory risk assess...

Hampton-Clarke, located in Fairfield, NJ, provides environmental field sampling services: air, soil and water. We have an immediate need for an experienced Environmental Field Services Manager. JOB RESPONSIBILITIES SUMMARY The Manager will manage the day-to-day activities of the Field Services department. Manager will be responsible for the overseeing and managing of multiple site-specific field a...

Regulatory CMC Specialist Job Summary Leading global pharma organisation is seeking a Senior Regulatory CMC specialist, who has a proven track record of Regulatory Strategy and Regulatory Submissions process (Regulatory/Submissions/CMC) to join the Regulatory Affairs team. This is a 12 month contract based out of Princeton, NJ. Key Activities: Provides strategic regulatory input and regulatory ris...

Manufacturing Supervisor-Verona, WI A globally recognized name in Active Pharmaceutical Ingredients is looking for a Manufacturing Supervisor to join their growing team. As Manufacturing Supervisor you will be responsible for all production activities including: planning and scheduling of production resources, troubleshooting process chemistry, training employees on equipment operation, assisting...

Job Description RESEARCH SUPPORT ASSOCIATE II, Koch Institute for Integrative Cancer Research-Hammond Lab, to support and be part of an exciting team working in nanomaterials technology for cancer therapeutics. Will be responsible for in vitro techniques including cell culture, cell viability test, cell labeling, immunostaining and imaging (microscope and FACS), and western and northern blotting;...

Regulatory CMC Specialist Job Summary Leading global pharma organisation is seeking a Senior Regulatory CMC specialist, who has a proven track record of Regulatory Strategy and Regulatory Submissions process (Regulatory/Submissions/CMC) to join the Regulatory Affairs team. This is a 12 month contract based out of Framingham, MA. Key Activities: Provides strategic regulatory input and regulatory ri...

Job ID: 38503 Position Description: Clean Harbors is the leading provider of environmental, energy and industrial services throughout North America. The Company serves a diverse customer base, including a majority of the Fortune 500 companies, thousands of smaller private entities and numerous federal, state, provincial and local governmental agencies. Through its Safety-Kleen subsidiary, Clean Ha...