Codexis Biotech Jobs

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Senior R&D Engineer TEI Biosciences Inc. seeks for a highly driven engineer with a passion for product development and a proven track record of taking products from concept to launch. The successful candidate will have a biomedical/mechanical engineering background with experience developing polymer/biopolymer and tissue-based Medical Device products for human implantation. TEI Biosciences is an...
Hays has partnered with a global Biotech company seeking a Sr. Mechanical Engineer. The ideal candidate is innovative, dynamic and looking for a high growth opportunity. This company supports over 6,000 employees and works in over 110 countries around the world. The ideal candidate will manage product develop initiatives in Fluid Management (CFD) ranging from concept, engineering, testing and lau...
Job Title: Clinical Outsourcing Consultant Job Code: RCI-ESI-1891 Job location: Woodcliff Lake, NJ 07677 Duration: 12 Months JOB DESCRIPTION: Support client's internal customers in the development of outsourcing requirements for Phase I-IV global clinical trials Lead and support the qualification and evaluation process for new service providers Lead the process of Request for Proposal (RFP)...
Highly visible position for individual with an executive presence, high energy and passion. Base salary starts at $350,000 plus bonus and equity potential in the seven figures range. Full company paid family benefits, tuition reimbursement, first class travel, expense account, club membership and executive perquisites. Seeking Medical Doctor with drug development experience in the area of Oncol...
Senior Research Associate - Contract Local SF BioPharma company is looking for an excellent candidates with inhalation experience! If you have the experience below, please send your resume to us ASAP! Position Duties: · Liquid aerosol testing for nebulizer inhalation solution product · Late-stage development testing · Device development, packaging, and characterization · Develop protocols & ...
Seeking board-certified physician with significant experience in Endo Metabolics applied to pharmaceutical company medical affairs and late stage clinical development and solid key opinion leader relationships in the therapeutic area to translate and align commercial and scientific goals and objectives for multiple product launches. Shall: *** Interact extensively with medical advisory boards. ...
Our client is the world's leading chemical company. With more than 110,000 employees, six affiliate sites and approximately 380 additional production sites worldwide they serve customers and partners in almost all countries of the world. They combine economic success, social responsibility and environmental protection. Through science and innovation they enable customers in almost all industries t...
Abacus Service Corporation is a nation-wide staffing firm based out of Farmington Hills, Michigan that services Fortune 500 companies in varying industries across the US. Our client is looking for a Regulatory Affairs Manager in Wayne, PA. Job Title : Regulatory Affairs Manager Duration : 6 months contract (Possibility of an extension) Location : Wayne PA-19087 Job Description: Primary Duties...
Position for executive players only. Must have an executive presence, high energy and passion. Base compensation at $400,000 plus bonus and equity potential in the seven figures range, first class travel, expense account, club membership and executive perquisites. Seeking Medical Doctor with track record maintaining relationships with key stakeholders and leading: *** Phase IV Clinical Trial Pro...
Opening for a Pharmaceutical Buyer with Versatex! We are actively seeking results driven Pharmaceutical Buyer to join our diverse team!! We provide comprehensive procurement and supplier management solutions. We focus on managing suppliers that support the Consumer Products, Food & Beverage, and Health & Science industries. We deliver savings, compliance, and enhanced service. Role Summary/Purp...
This position is responsible for the performance of pharmaceutical formulation research and development activities; formulating of controlled release products; authors supporting process documentation (URS, SOPs, Change Control, etc.); Provide technical input for the documentation and execution of validation protocols; leading pharmaceutical process development and design; and/or participation in ...
Manage activities associated with regulatory approval of in vitro diagnostic medical devices. Responsible for activities which lead to and maintain domestic and international regulatory approval to market devices. Responsible for assessment of device changes for regulatory implications. ESSENTIAL FUNCTIONS: Provide support to currently marketed products, e.g., review engineering changes, labelin...
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 ...
Lead Medical Affairs strategies and tactics for post phase two and product launch of Therapeutic Endometabolic Products. Responsibilities: *** Ensure accurate and robust medical-scientific knowledge is shared with stakeholders and Key Opinion Leaders. *** Identify the gaps in medical and scientific support and implement initiatives to address them. *** Serve as internal medical expert and medi...
Seeking Medical Doctor with 10+ years of post phase three imunnology-dermatology experience for commercial projects and promotional strategies including experience reviewing, approving and overseeing post marketing clinical studies to lead a US Medical Affairs team across a portfolio of autoimmune dermatology therapies providing strategic, operational, and medical leadership aligned with a patient...
Our client, a leading dermatologically-focused specialty pharmaceutical/medical device company, has engaged Hays Life Sciences to recruit for a Regulatory Affairs Director on a contract to hire basis. Our client has no pre-existing Regulatory department, giving this position an unmatched level of authority compared to other roles of this nature. This Director of Regulatory Affairs job is a unique ...
Job ID: 2458 Position Description: The Associate Director, Safety Information Management (SIM) manages the PVRM reporting and analysis function. The AD applies medical expertise and provides guidance to support case processing and aggregate reporting, and participates in proactive pharmacovigilance activities. Implements global guidelines concerning good pharmacovigilance practices including, b...
I have a very interesting Career Opportunity for a Hacker to take-on the duties of a Security Researcher / Online Threat Specialist / Malware Scientist who analyzes online security threats daily. You will be joining a recently well funded startup that is building anti-malware technologies for mobile devices and other systems that function online. You will analyze and research the various loopholes...
Fortune-500 Pharmaceutical / Biotech Company is seeking two motivated, experienced QC Analysts to join our team. We are seeking one QC Analyst with a focus in QC Microbiology and another with a focus in QC Chemistry. Below are the full details for both opportunities. QC Analyst – Microbiology: · Completes testing of raw materials, in-process and final products in accordance with SOPs for product...
This position is responsible for completing project tasks by carrying out laboratory experiments for assignments that are varied in nature. Responsibilities Laboratory Performs analysis on materials in support of cGMP activities. Performs responsibilities in compliance with Evonik quality systems. Maintains permanent records on all analyses performed and communicates results to appropriate Evo...

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