CD

Codexis

- NASDAQ:CDXS
Last Updated 2020-06-01

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Track Codexis hiring and firing trends, filtered by title, location, type, date, category and date of posting.
Ticker Symbol Entity Name Domain As Of Date Title URL Brand Category Location Text City State Country Posted Date Number of Openings Description Date Added Date Updated GICS Sector GICS Industry
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com May 21st, 2020 12:00AM Product Development Scientist Open 47 - MCE Redwood City CA USA Product Development scientistCross-disciplinary position that will work closely with a variety of groups including Molecular Biology, Biochemistry, Computational Biology, QC, Manufacturing, and Marketing to develop and validate reagents, consumables, and kits for the expansion of Codexis’ molecular diagnostics product portfolio.  Candidates must have a broad working knowledge of molecular biology and be able to apply that knowledge independently and creatively toward the development of novel workflows. Previous experience with product devolvement as demonstrated by work on launched products is essential. The successful applicant will have exceptional attention to detail and the ability to execute and analyze highly complex experiments. Key ResponsibilitiesDevelopment and optimization of novel reagents for applications such as amplification (linear and exponential), ligation and NGS library preparation workflows. Design and initiate long-term stability studies to establish high risk reagents/work flow/storage issues.Conceive, develop, validate, and implement new QC methods to assess reagents, consumables, and kits through a variety of analytical and functional tests.Independently troubleshoot and resolve reagent formulation, QC, and incoming material issues.Design and conduct experiments to determine underlying reaction mechanisms, cause and effect, failure modes, guard band studies and optimization using DOE methodologies.Data driven - critically analyze and derive insights from experimental data, using standard and custom bioinformatics tools. Present results and conclusions for internal review.Lead the technology transfer phase of the product pipeline as new products move from R&D into Manufacturing in preparation for commercial launch.Help design studies for customers testing Codexis’ products; interpret data and incorporate customer feedback into optimization and development experiments. Help build internal process development infrastructure across product lines.Demonstrate exceptional time management skills and a ‘can do’ approach to the challenges at hand.Author documents and protocols for manufacturing, protocols for QC and release specifications for each of the key reagents. Required Skills and BackgroundPhD in molecular biology, biochemistry, developmental biology, genetics, microbiology, cell biology, analytical chemistry, or related fields, with 3+ years relevant biotechnology or pharmaceutical industry experience in product or process development. M.Sc/B. Sc. with 8+ years relevant industry experience will be considered. In depth knowledge of molecular biology and analytical techniques including PCR, qRT-PCR, dPCR, FISH, PAGE, flow cytometry, CE, molecular cloning, nucleic acid isolation and manipulation, and NGS sample preparation technologies. Experience developing and implementing novel QC methods to assess reagent performance in both functional and orthogonal assays.Demonstrated record of successful technology transfer from early R&D concepts into customer-facing products.Experience with moving products from concept phase through commercial launch. Familiarity with commercialization phase-gate process.Demonstrated success in developing and optimizing novel molecular biology assays.Proven ability to write SOPs and train others to successfully perform the work.Exceptionally strong collaboration and communication skills. Desired Skills Experience using statistical tools, such as JMP to analyze complex data sets, create DOE experiments, and data trending.Experience operating liquid handling robots and other laboratory automation tools. Experience programming these instruments would be highly beneficial.Experience working with microfluidic devices.Experience with custom reagent vendors and setting up OEM relationships.Knowledge of current and evolving trends in the NGS field.  The position comes with a competitive compensation and benefits package, including paid company holidays, paid time off, health benefits, 401k match, and much more.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com.EOEPRINCIPALS ONLYNO AGENCIES OR THIRD PARTIES May 21st, 2020 01:00AM May 21st, 2020 01:00AM Basic Materials Chemicals
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com May 21st, 2020 12:00AM Research Associate, Process Development-Downstream Open 49 - Fermentation R&D Redwood City CA USA Downstream Process Development Research Associate  Codexis, Inc. (Nasdaq: CDXS) is a protein engineering industry leader with successful track record of developing novel enzymes used as biocatalysts for the commercial production of small molecule pharmaceuticals, diagnostic tools, chemicals used in the food industry, as well as multiple other applications. Codexis has also applied its CodeEvolver technology platform to discover and develop novel biotherapeutics for the treatment of rare genetic disorders, among other indications with significant unmet medical need.   Position Description:  The Process Development Associate will be responsible for the development, optimization, and scale-up of protein purification processes. The ideal candidate will have experience with the optimization of enzyme recovery/purification processes.   Responsibilities Include: Perform protein recovery experiments using unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration.Perform resin screening, column chromatography (IEX, HIC, MMC, CHT etc.).Analyze processing samples, using biological, biochemical, and other relevant analytical methods.Communicate results of experiments to the Project team.Participate in daily operation and routine maintenance/housekeeping of process and analytical equipment.Maintain a clean, organized and tidy lab environment. Order, resource, and stock chemicals and lab consumables.Maintain lab notebooks, write reports and SOPs. Job Requirements: University degree in Chemical Engineering, Biochemistry, or related discipline with a minimum of 2-4 years or Master’s degree with 1-2 years of experience in downstream process development lab, preferably enzyme, recombinant protein recovery, chromatography, and TFF unit operations.Experience with DSP unit operations such as homogenization, centrifugation, depth filtration, tangential flow filtration, ion exchange chromatography.Strong Biochemistry and Analytical Chemistry skills with experience in various assay techniques such as HPLC, enzyme activity assays, protein assays, etc.Some knowledge of Quality by Design (QbD) or Design of Experiments (DOE) approaches to process development is desirable.Experience with pilot-scale DSP equipment is a plus. Experience with lyophilization process development is a plus.Excellent interpersonal and communication (oral and written) skills, documentation, organization, good record keeping, writing reports and SOPs.Ability to prioritize responsibilities, multi-task, growth mindset, and remaining flexible with changing needs.Must be motivated and able to work under tight deadlines.Attention to detail, safety and good laboratory practice. The position comes with a competitive compensation and benefits package.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com. EOEPRINCIPALS ONLY NO AGENCIES OR THIRD PARTIES May 21st, 2020 01:00AM May 21st, 2020 01:00AM Basic Materials Chemicals
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com May 21st, 2020 12:00AM Research Associate, Process Development-Upstream Open 49 - Fermentation R&D Redwood City CA USA Upstream Process Development Research Associate  Codexis, Inc. (Nasdaq: CDXS) is a protein engineering industry leader with successful track record of developing novel enzymes used as biocatalysts for the commercial production of small molecule pharmaceuticals, diagnostic tools, chemicals used in the food industry, as well as multiple other applications. Codexis has also applied its CodeEvolver technology platform to discover and develop novel biotherapeutics for the treatment of rare genetic disorders, among other indications with significant unmet medical need.   Position Description:  Codexis is seeking a research associate to work within the Bioprocess Development team. This position will focus on microbial fermentation process development and primary recovery for recombinant protein production, and will be part of a dynamic team responsible for bioprocess development, scale up, and tech transfer of enzyme product manufacturing. Responsibilities Include: Conduct fermentation experiments by performing bioreactor setup and sampling Perform protein recovery experiments using unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration. Analyze processing samples, using biological, biochemical, and analytical chemistry assay techniques.Communicate results of experiments to the Project teamParticipate in daily operation and routine maintenance/housekeeping of process and analytical equipment.Maintain a clean, organized and tidy lab environment. Chemicals and consumables stocking, etc.Maintain lab notebooks, write reports and SOPs. Job Requirements: University degree in Chemical Engineering, Biochemistry, or related discipline with a minimum of 2 years experience in development of microbial fermentation processes.Experience with DSP unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration is a plus. Strong Biochemistry and Analytical Chemistry skills with experience in various assay techniques such as HPLC, enzyme activity assays, protein assays, etc.Excellent interpersonal and communication (oral and written) skills, documentation, organization, good record keeping, writing reports and SOPs.Ability to prioritize responsibilities, multi-task and remain flexible with changing needs.Must be motivated and able to work under tight deadlines.Attention to detail, safety and good laboratory practice.  The position comes with a competitive compensation and benefits package.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com. EOEPRINCIPALS ONLY NO AGENCIES OR THIRD PARTIES May 21st, 2020 01:00AM May 21st, 2020 01:00AM Basic Materials Chemicals
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com May 21st, 2020 12:00AM Product Manager, Research Enzymes Open 60 - Business Operations Redwood City CA USA Product Manager, Research EnzymesThis position is critical to both day-to-day and longer-term strategic success of Codexis’ Research Enzyme Business (REB). The REB is both a direct-to-customer catalog business and also a critical follow on from many of the research projects the company undertakes in its Performance Enzymes business unit, which encompasses  small molecule pharmaceuticals, food and nutrition, personal care, life sciences and industrial enzyme applications. The Product Manager will be accountable for the REB product portfolio and will own the upgrading and management of the business plan for the Research Enzyme Business, including management of the product lifecycles, competitive strategy, marketing planning, promotion and pricing.  Working very closely with business leaders, technical project teams, manufacturing teams and the operational and quality functions, the role will be involved in much of the technical and operational management of product development and commercialization projects within the Performance Enzyme business unit. The ideal candidate will be a self-starter with a biotechnical background, preferably in enzyme production and/or technical program management. The ideal candidate will thrive in a dynamic and diverse environment and will be adaptable, highly accountable, detail focused, results oriented and strong in analytical and critical thinking. Most importantly, the candidate will be able to prioritize effectively across multiple objectives and have the ability to interact with and influence a wide range of stakeholders across functions and across multiple levels. Responsibilities:Own the generation and management of the business plan for the catalog Research Enzyme Business (REB), including outlining product requirements for new enzyme screening products, strategy development and stakeholder sign-off. Collaborate with Supply Chain, Manufacturing and Quality teams to schedule and prioritize product manufacture to ensure products are and delivered, within specification, on time to customers and that suitable inventories of catalog products are maintained.Collaborate with internal research and development, legal, intellectual property and finance to manage operational deliverables in programs and support contracts compliance. Participate on cross functional teams for continuous improvement of business processes.Conduct analysis and communicate summaries of sales and customer-usage trends within the business unit; use the analysis to drive customer follow-up with BD. Evaluate industry trends and developments including competitor, customer and market analysis to ensure Codexis addresses opportunities and threats in an effective way. Preparation of information on product features and benefits for use in marketing literature, client meetings and other relevant market-facing channels; attend client meetings as appropriate. Provide input to marketing and business development team to support the development of marketing plans and of long and short-term marketing strategies. Requirements:BA/BS in the life sciences or a related discipline required; a business degree or other business qualification, in addition, is desirable.3+ years of biotech R&D, product management, business development, or related experience required.Demonstrated competence with MS Office, including MS Word, Excel, Powerpoint and Project required.Project management experience is highly desirable.Experience with product lifecycle management from launch through obsolescence, including strategic market planning, competitive strategy, and management of pricing is desired.Experience using CRM software or other tools to communicate, manage and continuously improve business performance is desired; Salesforce experience is a plus.The position comes with a competitive compensation and benefits package, including paid company holidays, paid time off, health benefits, 401k match, and much more.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com.EOEPRINCIPALS ONLYNO AGENCIES OR THIRD PARTIES May 21st, 2020 01:00AM May 21st, 2020 01:00AM Basic Materials Chemicals
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com Mar 27th, 2020 12:00AM Translational Scientist Open 40 - New Molecular Entities Redwood City CA USA Translational ScientistCodexis, Inc. (Nasdaq: CDXS) is a protein engineering industry leader with successful track record of developing novel enzymes used as biocatalysts for the commercial production of small molecule pharmaceuticals, chemicals used in the food industry, as well as multiple other applications. Codexis has applied its CodeEvolver technology platform to discover and develop novel biotherapeutics for the treatment of rare genetic disorders, among other indications with significant unmet medical need. In 2017 the company announced a broad collaboration with Nestle Health Science, in which Nestle took an option to co-develop and potentially commercialize Codexis’ first self-developed therapeutic candidate, CDX-6114 for the treatment of Phenylketonuria (PKU), and also gained access to employ Codex’ protein engineering platform in a multi-project partnership for the discovery and development of new therapeutically relevant enzymes. This transaction marked the company’s first partnership for an internally developed biotherapeutic product, and validated the CodeEvolver protein engineering platform as a biotherapeutic discovery engine.  We are currently seeking a highly motivated Translational Scientist who will be responsible for effective bridging of our core enzyme optimization programs with ex vivo and in vivo preclinical studies. Successful candidates will be part of a growing interdisciplinary, dynamic and enthusiastic team responsible for further expanding Codexis’ biotherapeutic project portfolio and maximizing Codexis’ core technologies for the design, optimization and validation of protein therapeutics.   Primary responsibilities include:Integrate preclinical drug development studies into Codexis’ core workflows. Identifying, developing, and managing external collaborators (academic, industrial partners, and CROs) to support preclinical development programs. Collaborate with CRO’s/KOL’s to develop animal models relevant to programs.Design and execution of PK/PD and efficacy studies. Understand and support/conduct the in vitro assays necessary to move programs forward, participate where appropriate in design. Experience in immunogenicity assays a plus.Identification and validation of translational biomarkers ahead of moving to clinical trials.Maintains a current understanding of the scientific literature related to rare diseases where therapeutic enzymes and proteins could be impactful. Represent the Translational Biology group within project teams.Excellent and effective oral and written communication with Codexis R&D, senior leadership, and external collaborators.Participate in discussions with KOL’s to obtain feedback on preclinical development programs.  Desired Skills and ExperiencePhD preferably in Biology or Pharmacology plus 2+ years’ experience in preclinical drug development.  Hands-on experience with in vivo pharmacology highly desired, as well as experience in rare diseases where enzymes/proteins are therapies. An excellent scientific background as demonstrated through publications in top peer-reviewed journals. Successful track record of working with consultants, academic collaborations, and CROs. The position comes with a competitive compensation and benefits package, including paid company holidays, paid time off, health benefits, 401k match, and much more.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com.EOEPRINCIPALS ONLYNO AGENCIES OR THIRD PARTIES Mar 26th, 2020 11:11PM Mar 26th, 2020 11:11PM Basic Materials Chemicals
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com Mar 27th, 2020 12:00AM Research Associate, Biotherapeutics Lead Discovery Open 41 - Biochemistry Redwood City CA USA Research Associate 2/Senior Research Associate, Biotherapeutics Lead DiscoveryCodexis seeks a highly motivated research associate to join the Biotherapeutics Lead Discovery group to support our efforts to engineer novel biotherapeutic proteins. We are looking for an experienced scientific researcher proficient in protein biochemistry and analytical methods development. Successful candidates will be part of an interdisciplinary, dynamic and enthusiastic biotherapeutics discovery team responsible for implementing Codexis’ core technologies and delivering candidate biologics. Responsibilities include:Express and purify recombinant proteins at research scale from mammalian and E. coli systemsCharacterize purified proteins using standard analytical and biophysical techniques, including SDS-PAGE, Western Blot, ELISA, intact mass, size-exclusion chromatography, and melting temperature measurementCharacterize proteins in biochemical assaysMaintain a safe and efficient workplace, follow safe lab practices, keep diligent records, and write reports and SOPs as neededActively participate in project teams, present research updates, and collaborate with cross-functional team members. Job Requirements:BS with 5+ years of relevant experience or MS degree with 3+ years of experience in Biochemistry, Bioengineering, Molecular Biology, Cell Biology, or related field; industry experience strongly preferred. Level of hiring will be based on the candidate’s experience and capabilitiesKnowledge of recombinant expression in bacteria and mammalian cellsFamiliarity with mammalian cell culture and sterile techniquesHands-on protein purification expertise, including developing methods for untagged proteins. Experience operating AKTA FPLC systems strongly desiredExperience characterizing therapeutic proteins by analytical methods, ELISA, cell-based assays, high-content imaging, or related techniques is highly desiredHighly organized, attentive to detail, and able to work under tight timelines in a collaborative team settingExcellent interpersonal and communication skills The position comes with a competitive compensation and benefits package, including paid company holidays, paid time off, health benefits, 401k match, and much more.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com.EOEPRINCIPALS ONLYNO AGENCIES OR THIRD PARTIES Mar 26th, 2020 11:11PM Mar 26th, 2020 11:11PM Basic Materials Chemicals
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com Mar 27th, 2020 12:00AM Research Associate, Process Development-Downstream Open 49 - Fermentation R&D Redwood City CA USA Downstream Process Development Research Associate  Codexis, Inc. (Nasdaq: CDXS) is a protein engineering industry leader with successful track record of developing novel enzymes used as biocatalysts for the commercial production of small molecule pharmaceuticals, diagnostic tools, chemicals used in the food industry, as well as multiple other applications. Codexis has also applied its CodeEvolver technology platform to discover and develop novel biotherapeutics for the treatment of rare genetic disorders, among other indications with significant unmet medical need.   Position Description:  The Process Development Associate will be responsible for the development, optimization, and scale-up of protein purification processes. The ideal candidate will have experience with the optimization of enzyme recovery/purification processes.   Responsibilities Include: Perform protein recovery experiments using unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration.Perform resin screening, column chromatography (IEX, HIC, MMC, CHT etc.).Analyze processing samples, using biological, biochemical, and other relevant analytical methods.Communicate results of experiments to the Project team.Participate in daily operation and routine maintenance/housekeeping of process and analytical equipment.Maintain a clean, organized and tidy lab environment. Order, resource, and stock chemicals and lab consumables.Maintain lab notebooks, write reports and SOPs. Job Requirements: University degree in Chemical Engineering, Biochemistry, or related discipline with a minimum of 2-4 years or Master’s degree with 1-2 years of experience in downstream process development lab, preferably enzyme, recombinant protein recovery, chromatography, and TFF unit operations.Experience with DSP unit operations such as homogenization, centrifugation, depth filtration, tangential flow filtration, ion exchange chromatography.Strong Biochemistry and Analytical Chemistry skills with experience in various assay techniques such as HPLC, enzyme activity assays, protein assays, etc.Some knowledge of Quality by Design (QbD) or Design of Experiments (DOE) approaches to process development is desirable.Experience with pilot-scale DSP equipment is a plus. Experience with lyophilization process development is a plus.Excellent interpersonal and communication (oral and written) skills, documentation, organization, good record keeping, writing reports and SOPs.Ability to prioritize responsibilities, multi-task, growth mindset, and remaining flexible with changing needs.Must be motivated and able to work under tight deadlines.Attention to detail, safety and good laboratory practice. The position comes with a competitive compensation and benefits package.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com. EOEPRINCIPALS ONLY NO AGENCIES OR THIRD PARTIES Mar 26th, 2020 11:11PM Mar 26th, 2020 11:11PM Basic Materials Chemicals
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com Mar 27th, 2020 12:00AM Research Associate, Process Development-Upstream Open 49 - Fermentation R&D Redwood City CA USA Upstream Process Development Research Associate  Codexis, Inc. (Nasdaq: CDXS) is a protein engineering industry leader with successful track record of developing novel enzymes used as biocatalysts for the commercial production of small molecule pharmaceuticals, diagnostic tools, chemicals used in the food industry, as well as multiple other applications. Codexis has also applied its CodeEvolver technology platform to discover and develop novel biotherapeutics for the treatment of rare genetic disorders, among other indications with significant unmet medical need.   Position Description:  Codexis is seeking a research associate to work within the Bioprocess Development team. This position will focus on microbial fermentation process development and primary recovery for recombinant protein production, and will be part of a dynamic team responsible for bioprocess development, scale up, and tech transfer of enzyme product manufacturing. Responsibilities Include: Conduct fermentation experiments by performing bioreactor setup and sampling Perform protein recovery experiments using unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration. Analyze processing samples, using biological, biochemical, and analytical chemistry assay techniques.Communicate results of experiments to the Project teamParticipate in daily operation and routine maintenance/housekeeping of process and analytical equipment.Maintain a clean, organized and tidy lab environment. Chemicals and consumables stocking, etc.Maintain lab notebooks, write reports and SOPs. Job Requirements: University degree in Chemical Engineering, Biochemistry, or related discipline with a minimum of 2 years experience in development of microbial fermentation processes.Experience with DSP unit operations such as homogenization, centrifugation, depth filtration, microfiltration, and ultrafiltration is a plus. Strong Biochemistry and Analytical Chemistry skills with experience in various assay techniques such as HPLC, enzyme activity assays, protein assays, etc.Excellent interpersonal and communication (oral and written) skills, documentation, organization, good record keeping, writing reports and SOPs.Ability to prioritize responsibilities, multi-task and remain flexible with changing needs.Must be motivated and able to work under tight deadlines.Attention to detail, safety and good laboratory practice.  The position comes with a competitive compensation and benefits package.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com. EOEPRINCIPALS ONLY NO AGENCIES OR THIRD PARTIES Mar 26th, 2020 11:11PM Mar 26th, 2020 11:11PM Basic Materials Chemicals
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com Mar 27th, 2020 12:00AM Product Manager, Research Enzymes Open 60 - Business Operations Redwood City CA USA Product Manager, Research EnzymesThis position is critical to both day-to-day and longer-term strategic success of Codexis’ Research Enzyme Business (REB). The REB is both a direct-to-customer catalog business and also a critical follow on from many of the research projects the company undertakes in its Performance Enzymes business unit, which encompasses  small molecule pharmaceuticals, food and nutrition, personal care, life sciences and industrial enzyme applications. The Product Manager will be accountable for the REB product portfolio and will own the upgrading and management of the business plan for the Research Enzyme Business, including management of the product lifecycles, competitive strategy, marketing planning, promotion and pricing.  Working very closely with business leaders, technical project teams, manufacturing teams and the operational and quality functions, the role will be involved in much of the technical and operational management of product development and commercialization projects within the Performance Enzyme business unit. The ideal candidate will be a self-starter with a biotechnical background, preferably in enzyme production and/or technical program management. The ideal candidate will thrive in a dynamic and diverse environment and will be adaptable, highly accountable, detail focused, results oriented and strong in analytical and critical thinking. Most importantly, the candidate will be able to prioritize effectively across multiple objectives and have the ability to interact with and influence a wide range of stakeholders across functions and across multiple levels. Responsibilities:Own the generation and management of the business plan for the catalog Research Enzyme Business (REB), including outlining product requirements for new enzyme screening products, strategy development and stakeholder sign-off. Collaborate with Supply Chain, Manufacturing and Quality teams to schedule and prioritize product manufacture to ensure products are and delivered, within specification, on time to customers and that suitable inventories of catalog products are maintained.Collaborate with internal research and development, legal, intellectual property and finance to manage operational deliverables in programs and support contracts compliance. Participate on cross functional teams for continuous improvement of business processes.Conduct analysis and communicate summaries of sales and customer-usage trends within the business unit; use the analysis to drive customer follow-up with BD. Evaluate industry trends and developments including competitor, customer and market analysis to ensure Codexis addresses opportunities and threats in an effective way. Preparation of information on product features and benefits for use in marketing literature, client meetings and other relevant market-facing channels; attend client meetings as appropriate. Provide input to marketing and business development team to support the development of marketing plans and of long and short-term marketing strategies. Requirements:BA/BS in the life sciences or a related discipline required; a business degree or other business qualification, in addition, is desirable.3+ years of biotech R&D, product management, business development, or related experience required.Demonstrated competence with MS Office, including MS Word, Excel, Powerpoint and Project required.Project management experience is highly desirable.Experience with product lifecycle management from launch through obsolescence, including strategic market planning, competitive strategy, and management of pricing is desired.Experience using CRM software or other tools to communicate, manage and continuously improve business performance is desired; Salesforce experience is a plus.The position comes with a competitive compensation and benefits package, including paid company holidays, paid time off, health benefits, 401k match, and much more.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com.EOEPRINCIPALS ONLYNO AGENCIES OR THIRD PARTIES Mar 26th, 2020 11:11PM Mar 26th, 2020 11:11PM Basic Materials Chemicals
nasdaq:cdxs codexis.applytojob.com codexis.applytojob.com Mar 27th, 2020 12:00AM Associate Director, Technical Operations Open 60-Business Operations Redwood City CA USA Codexis, Inc. (Nasdaq: CDXS) is a protein engineering industry leader with successful track record of developing novel enzymes used as biocatalysts for the commercial production of small molecule pharmaceuticals, chemicals used in the food industry, as well as multiple other applications. Codexis has also applied its CodeEvolver technology platform to discover and develop novel biotherapeutics for the treatment of rare genetic disorders, among other indications with significant unmet medical need.  The Associate Director, Technical Operations role is critical to the success of Codexis’ pharmaceutical development and manufacturing efforts in pre-clinical and early stage clinical drug substance and drug product development for Codexis’ self-developed enzyme therapeutics pipeline. Working very closely with technical project teams and the operational and quality functions, as well as with consultants as appropriate, this combined project leader/project manager role will be key to the successful technical and operational management of biotherapeutics development programs at Codexis.Major ResponsibilitiesCoordination of multi-functional development teams including research, translational biology, bioprocess development, analytical development, quality, formulation, toxicology and regulatory resources in order to efficiently execute against development goals and identify opportunities for acceleration of timelines.Project management of project teams through scheduling of meetings, facilitation of communication; minuting of meeting decisions and action items; development of project scope, timelines, and deliverables; and identification of resource requirements.Building and managing project budgets including review of invoices and amending budget, revenue and expense forecasts. Critical involvement in identification and selection of CRO and CDMO partners for outsourced development and manufacture of drug substance and drug product through development of business intelligence on potential CRO and CDMO partners, preparation of RFPs, review of proposals, and participation in contract negotiations.Management of CRO and CDMO relationships in order to achieve the successful completion of project specific activities and timely achievement of project milestones.Management of the identification, calibration, mitigation and escalation of risks in the development, technology transfer and scale-up of drug substance and drug product at Biotherapeutic CDMOs.Project managing IND-enabling studies and regulatory submissions (IND or other) for Phase 1 clinical studies.Minimum RequirementsMinimum of either a PhD with 5 years of experience or a BS/BA (in biochemistry, chemistry, bioengineering or a related discipline) with 10 years of experience in CMC related pharmaceutical development roles in an industrial environment.  GMP experience strongly preferred.Drug substance development experience with biotherapeutic molecules essential and drug product development experience preferred.  Knowledge of enzymes desired.Experience with a range of biologic manufacturing expression systems desired – ideally including both microbial and mammalian strains.Experience managing external CRO/CDMO/CMO relationships required, ideally including demonstrated experience running vendor selection processes and contract/scope negotiations.Experience preparing and supporting early phase regulatory filings strongly preferred – IND strongly preferred and knowledge of regulatory submission in other geographies desired.Excellent communication skills (written and verbal)Strong project management experience and skillsExpertise in using MS Office, including MS Project, essentialMust be able to travel internationally and domestically a minimum of 10% of the timePMP certification desired The position comes with a competitive compensation and benefits package, including paid company holidays, paid time off, health benefits, 401k match, and much more.  For more information about our plans for the future, and to be considered for this career opportunity, please visit www.codexis.com.EOEPRINCIPALS ONLYNO AGENCIES OR THIRD PARTIES Mar 26th, 2020 11:11PM Mar 26th, 2020 11:11PM Basic Materials Chemicals

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