NV

Novavax

- NASDAQ:NVAX
Last Updated 2019-07-19

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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 Ticker Sector Ticker Industry
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 5th, 2018 12:00AM Quality Systems Specialist IV (Temporary Assignment) Open Novavax CONTRACTOR Gaithersburg MD USA Jul 13th, 2018 12:00AM At Novavax, a clinical-stage vaccine company, we are creating tomorrow's vaccines today! We seek to attract, develop, and retain talented people who share our passion for science, medicine, and human health. We foster an environment of teamwork and collaboration, built on a culture that values and appreciates its employees. We are a fast-paced company that provides employees with opportunities to achieve personal and professional goals while also maintaining a balance between work and personal life. We are seeking a temporary Quality Systems Specialist to join our Quality Systems group to perform a variety of activities to ensure the safety, quality, and efficacy of our product. The Quality System Specialist will be responsible for general support and maintenance of the Quality System within the requirements of FDA Quality System Regulation (QSR). The primary duties for this individual will be to review and approve laboratory investigations, deviations and CAPA and support the Change Control program. Additional functions include writing and revising standard operating procedures, training, and tracking and trending data. Duties for this position support Manufacturing, Quality Control, Quality Assurance, product release, and training.   Responsibilities include but are not limited to:  Monitor, review and approve laboratory investigations, deviations and CAPA (including CAPA effectiveness checks) in the Quality Management System. Track and trend Quality System Data. Perform Root Cause Analysis. Review of change controls for content and completeness. Generate and update standard operating procedures to define and improve quality system functions. Participate in the implementation and monitoring of the QMS training program. Interface with other departments regarding documentation requirements and complex investigations. Prepares information related to the state of the QMS to be used in routine monthly reporting and Quality Council meetings. Proactively, based on data analysis, recommends to management areas of improvement within the various operations. Participate in continuous improvement projects as required.   Minimum Requirements:  Bachelor's Degree in a relevant life science field such as Biology, Microbiology, Chemistry, Biochemistry, etc. with at least 8 years of working experience in Quality Assurance, Quality Control or Manufacturing. Previous professional experience with cGMPs and associated regulatory compliance requirements and guidelines for the manufacture, testing, and release of pharmaceutical or biopharmaceutical products. Knowledge of FDA requirements including 21CFR210, 211 and Quality System Regulations. Able to rapidly adapt to changing environment and circumstances requiring flexibility, tolerance and great sense of urgency while ensuring that all cGMP and Regulatory requirement are met. Experience in compiling data to support metrics analyzing current processes. Proficiency with Word, Excel and Power Point.   Additionally, we prefer candidate that have: The ability to effectively build and maintain relationships with multiple departments in order to effectively solve problems. The ability to lead teams and meetings and represent Quality at cross-functional meetings. Must exercise accurate judgment and be able to evaluate information critically and decide upon appropriate course of action. Must be able to correlate events and determine the action plan required to avoid incidents recurrence and or regulatory exposure. The ability to organize, prioritize and deliver tasks & projects with a sense of urgency under minimal supervision with neglecting attention to detail. The ability to enable and drive change while being focused on internal and external customers. The ability to communicate well both verbally and in writing with all levels both inside and outside of the organization. Prior experience with Lean Six Sigma. Capable to manage multiple priorities.   Novavax, Inc. is a clinical-stage biotechnology company committed to delivering novel products to prevent a broad range of infectious diseases. Using innovative proprietary recombinant nanoparticle vaccine technology, we produce vaccine candidates to efficiently and effectively respond to both known and emerging disease threats. Our vaccine candidates are genetically engineered three-dimensional nanostructures that incorporate recombinant proteins critical to disease pathogenesis. Our product pipeline targets a variety of infectious diseases, with clinical vaccine candidates for respiratory syncytial virus (RSV) and Ebola virus (EBOV), and preclinical programs for Zika virus (ZIKV), seasonal influenza and a combination respiratory vaccine candidate, as well as other infectious disease vaccine candidates. Novavax, Inc. is headquartered in Gaithersburg, Maryland with additional facilities in Rockville, Maryland and Uppsala, Sweden. Novavax is traded on the Nasdaq Stock Market under the symbol NVAX and is dedicated to developing novel vaccines to address infectious disease. Novavax, Inc. offers a base salary, annual bonus, stock options, professional career development/growth opportunities, and a comprehensive benefits package including medical, dental, vision, Rx, STD, LTD, Life, Optional Life, 401(k) plan.   Equal Opportunity Employer/Veterans/Disabled Novavax, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Aug 5th, 2018 07:53AM Aug 5th, 2018 07:53AM Health Care Pharmaceuticals & Biotechnology
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 5th, 2018 12:00AM Scientist, Analytical Development (Contract) Open Novavax CONTRACTOR Gaithersburg MD USA Jul 30th, 2018 12:00AM The candidate will work in the Characterization group support one or two projects related to RSV F or Nano HA. The candidate will work in the lab using methods such as liquid chromatography, dynamic light scattering, and analytical ultracentrifugation and will assist in various studies supporting characterization of the Nano HA and RSV F products. The candidate will organize and present data in meetings and will work closely with other members of the Characterization group. Minimum requirements: Undergraduate or graduate degree in a related field of science (e.g. chemistry, biochemistry, biophysics) At least five years of lab research experience, with supporting record of peer-reviewed publications Experience in methods for protein characterization, including HPLC separations based on size, charge, or hydrophobicity Analytical Ultracentrifugation (AUC) of biomolecules or nanoparticles Dynamic Light Scattering (DLS) of proteins or nanoparticles Proficient with Microsoft Office programs Excellent organizational, verbal, and written communication skills Detail oriented and self-motivated Aug 5th, 2018 07:53AM Aug 5th, 2018 07:53AM Health Care Pharmaceuticals & Biotechnology
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 6th, 2018 12:00AM Analytical Development Associate II (Contract) Open Novavax CONTRACTOR Gaithersburg MD USA Jun 19th, 2018 12:00AM At Novavax, a clinical-stage vaccine company, we are creating tomorrow's vaccines today! We seek to attract, develop, and retain talented people who share our passion for science, medicine, and human health. We foster an environment of teamwork and collaboration, built on a culture that values and appreciates its employees. We are a fast-paced company that provides employees with opportunities to achieve personal and professional goals while also maintaining a balance between work and personal life. We are currently looking for an Analaytical Associate II to work as a part of our Molecular and Cellular Virology Group, within the Analytical Development Department. The successful candidate will report a team leader in the Molecular and Cellular Virology Group. The successful candidate will be responsible for in-process sample testing, detecting infectious, and potency assays. The candidate will make detailed observations, analyze data, and interpret results. The candidate will receive general instructions from a supervisor for routine work and new assignments                                                                                                                                  Duration: July 2018-December 2018, with possibility for extension   Minimum requirements:  BS degree in a relevant scientific discipline with 2+ years relevant industry experience MS degree in a relevant scientific discipline with 1+ years of relevant industry experience Experience recording data according to Good Documentation Practices Standards Ability to plan and perform complex procedures and experiments Experience analyzing and interpreting data Proficiency in Microsoft Word, PowerPoint, Excel Proficiency with statistical software is a plus   Novavax, Inc. is a clinical-stage biotechnology company committed to delivering novel products to prevent a broad range of infectious diseases. Using innovative proprietary recombinant nanoparticle vaccine technology, we produce vaccine candidates to efficiently and effectively respond to both known and emerging disease threats. Our vaccine candidates are genetically engineered three-dimensional nanostructures that incorporate recombinant proteins critical to disease pathogenesis. Our product pipeline targets a variety of infectious diseases, with clinical vaccine candidates for respiratory syncytial virus (RSV) and Ebola virus (EBOV), and preclinical programs for Zika virus (ZIKV), seasonal influenza and a combination respiratory vaccine candidate, as well as other infectious disease vaccine candidates. Novavax, Inc. is headquartered in Gaithersburg, Maryland with additional facilities in Rockville, Maryland and Uppsala, Sweden. Novavax is traded on the Nasdaq Stock Market under the symbol NVAX and is dedicated to developing novel vaccines to address infectious disease.   Equal Opportunity Employer/Veterans/Disabled Novavax, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Aug 6th, 2018 07:46AM Aug 6th, 2018 07:46AM Health Care Pharmaceuticals & Biotechnology
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 6th, 2018 12:00AM Quality Systems Specialist IV (Temporary Assignment) Open Novavax CONTRACTOR Gaithersburg MD USA Jul 13th, 2018 12:00AM At Novavax, a clinical-stage vaccine company, we are creating tomorrow's vaccines today! We seek to attract, develop, and retain talented people who share our passion for science, medicine, and human health. We foster an environment of teamwork and collaboration, built on a culture that values and appreciates its employees. We are a fast-paced company that provides employees with opportunities to achieve personal and professional goals while also maintaining a balance between work and personal life. We are seeking a temporary Quality Systems Specialist to join our Quality Systems group to perform a variety of activities to ensure the safety, quality, and efficacy of our product. The Quality System Specialist will be responsible for general support and maintenance of the Quality System within the requirements of FDA Quality System Regulation (QSR). The primary duties for this individual will be to review and approve laboratory investigations, deviations and CAPA and support the Change Control program. Additional functions include writing and revising standard operating procedures, training, and tracking and trending data. Duties for this position support Manufacturing, Quality Control, Quality Assurance, product release, and training.   Responsibilities include but are not limited to:  Monitor, review and approve laboratory investigations, deviations and CAPA (including CAPA effectiveness checks) in the Quality Management System. Track and trend Quality System Data. Perform Root Cause Analysis. Review of change controls for content and completeness. Generate and update standard operating procedures to define and improve quality system functions. Participate in the implementation and monitoring of the QMS training program. Interface with other departments regarding documentation requirements and complex investigations. Prepares information related to the state of the QMS to be used in routine monthly reporting and Quality Council meetings. Proactively, based on data analysis, recommends to management areas of improvement within the various operations. Participate in continuous improvement projects as required.   Minimum Requirements:  Bachelor's Degree in a relevant life science field such as Biology, Microbiology, Chemistry, Biochemistry, etc. with at least 8 years of working experience in Quality Assurance, Quality Control or Manufacturing. Previous professional experience with cGMPs and associated regulatory compliance requirements and guidelines for the manufacture, testing, and release of pharmaceutical or biopharmaceutical products. Knowledge of FDA requirements including 21CFR210, 211 and Quality System Regulations. Able to rapidly adapt to changing environment and circumstances requiring flexibility, tolerance and great sense of urgency while ensuring that all cGMP and Regulatory requirement are met. Experience in compiling data to support metrics analyzing current processes. Proficiency with Word, Excel and Power Point.   Additionally, we prefer candidate that have: The ability to effectively build and maintain relationships with multiple departments in order to effectively solve problems. The ability to lead teams and meetings and represent Quality at cross-functional meetings. Must exercise accurate judgment and be able to evaluate information critically and decide upon appropriate course of action. Must be able to correlate events and determine the action plan required to avoid incidents recurrence and or regulatory exposure. The ability to organize, prioritize and deliver tasks & projects with a sense of urgency under minimal supervision with neglecting attention to detail. The ability to enable and drive change while being focused on internal and external customers. The ability to communicate well both verbally and in writing with all levels both inside and outside of the organization. Prior experience with Lean Six Sigma. Capable to manage multiple priorities.   Novavax, Inc. is a clinical-stage biotechnology company committed to delivering novel products to prevent a broad range of infectious diseases. Using innovative proprietary recombinant nanoparticle vaccine technology, we produce vaccine candidates to efficiently and effectively respond to both known and emerging disease threats. Our vaccine candidates are genetically engineered three-dimensional nanostructures that incorporate recombinant proteins critical to disease pathogenesis. Our product pipeline targets a variety of infectious diseases, with clinical vaccine candidates for respiratory syncytial virus (RSV) and Ebola virus (EBOV), and preclinical programs for Zika virus (ZIKV), seasonal influenza and a combination respiratory vaccine candidate, as well as other infectious disease vaccine candidates. Novavax, Inc. is headquartered in Gaithersburg, Maryland with additional facilities in Rockville, Maryland and Uppsala, Sweden. Novavax is traded on the Nasdaq Stock Market under the symbol NVAX and is dedicated to developing novel vaccines to address infectious disease. Novavax, Inc. offers a base salary, annual bonus, stock options, professional career development/growth opportunities, and a comprehensive benefits package including medical, dental, vision, Rx, STD, LTD, Life, Optional Life, 401(k) plan.   Equal Opportunity Employer/Veterans/Disabled Novavax, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Aug 6th, 2018 07:46AM Aug 6th, 2018 07:46AM Health Care Pharmaceuticals & Biotechnology
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 6th, 2018 12:00AM Scientist, Analytical Development (Contract) Open Novavax CONTRACTOR Gaithersburg MD USA Jul 30th, 2018 12:00AM The candidate will work in the Characterization group support one or two projects related to RSV F or Nano HA. The candidate will work in the lab using methods such as liquid chromatography, dynamic light scattering, and analytical ultracentrifugation and will assist in various studies supporting characterization of the Nano HA and RSV F products. The candidate will organize and present data in meetings and will work closely with other members of the Characterization group. Minimum requirements: Undergraduate or graduate degree in a related field of science (e.g. chemistry, biochemistry, biophysics) At least five years of lab research experience, with supporting record of peer-reviewed publications Experience in methods for protein characterization, including HPLC separations based on size, charge, or hydrophobicity Analytical Ultracentrifugation (AUC) of biomolecules or nanoparticles Dynamic Light Scattering (DLS) of proteins or nanoparticles Proficient with Microsoft Office programs Excellent organizational, verbal, and written communication skills Detail oriented and self-motivated Aug 6th, 2018 07:46AM Aug 6th, 2018 07:46AM Health Care Pharmaceuticals & Biotechnology
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 7th, 2018 12:00AM Analytical Development Associate II (Contract) Open Novavax CONTRACTOR Gaithersburg MD USA Jun 19th, 2018 12:00AM At Novavax, a clinical-stage vaccine company, we are creating tomorrow's vaccines today! We seek to attract, develop, and retain talented people who share our passion for science, medicine, and human health. We foster an environment of teamwork and collaboration, built on a culture that values and appreciates its employees. We are a fast-paced company that provides employees with opportunities to achieve personal and professional goals while also maintaining a balance between work and personal life. We are currently looking for an Analaytical Associate II to work as a part of our Molecular and Cellular Virology Group, within the Analytical Development Department. The successful candidate will report a team leader in the Molecular and Cellular Virology Group. The successful candidate will be responsible for in-process sample testing, detecting infectious, and potency assays. The candidate will make detailed observations, analyze data, and interpret results. The candidate will receive general instructions from a supervisor for routine work and new assignments                                                                                                                                  Duration: July 2018-December 2018, with possibility for extension   Minimum requirements:  BS degree in a relevant scientific discipline with 2+ years relevant industry experience MS degree in a relevant scientific discipline with 1+ years of relevant industry experience Experience recording data according to Good Documentation Practices Standards Ability to plan and perform complex procedures and experiments Experience analyzing and interpreting data Proficiency in Microsoft Word, PowerPoint, Excel Proficiency with statistical software is a plus   Novavax, Inc. is a clinical-stage biotechnology company committed to delivering novel products to prevent a broad range of infectious diseases. Using innovative proprietary recombinant nanoparticle vaccine technology, we produce vaccine candidates to efficiently and effectively respond to both known and emerging disease threats. Our vaccine candidates are genetically engineered three-dimensional nanostructures that incorporate recombinant proteins critical to disease pathogenesis. Our product pipeline targets a variety of infectious diseases, with clinical vaccine candidates for respiratory syncytial virus (RSV) and Ebola virus (EBOV), and preclinical programs for Zika virus (ZIKV), seasonal influenza and a combination respiratory vaccine candidate, as well as other infectious disease vaccine candidates. Novavax, Inc. is headquartered in Gaithersburg, Maryland with additional facilities in Rockville, Maryland and Uppsala, Sweden. Novavax is traded on the Nasdaq Stock Market under the symbol NVAX and is dedicated to developing novel vaccines to address infectious disease.   Equal Opportunity Employer/Veterans/Disabled Novavax, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Aug 7th, 2018 08:47AM Aug 7th, 2018 08:47AM Health Care Pharmaceuticals & Biotechnology
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 7th, 2018 12:00AM Quality Systems Specialist IV (Temporary Assignment) Open Novavax CONTRACTOR Gaithersburg MD USA Jul 13th, 2018 12:00AM At Novavax, a clinical-stage vaccine company, we are creating tomorrow's vaccines today! We seek to attract, develop, and retain talented people who share our passion for science, medicine, and human health. We foster an environment of teamwork and collaboration, built on a culture that values and appreciates its employees. We are a fast-paced company that provides employees with opportunities to achieve personal and professional goals while also maintaining a balance between work and personal life. We are seeking a temporary Quality Systems Specialist to join our Quality Systems group to perform a variety of activities to ensure the safety, quality, and efficacy of our product. The Quality System Specialist will be responsible for general support and maintenance of the Quality System within the requirements of FDA Quality System Regulation (QSR). The primary duties for this individual will be to review and approve laboratory investigations, deviations and CAPA and support the Change Control program. Additional functions include writing and revising standard operating procedures, training, and tracking and trending data. Duties for this position support Manufacturing, Quality Control, Quality Assurance, product release, and training.   Responsibilities include but are not limited to:  Monitor, review and approve laboratory investigations, deviations and CAPA (including CAPA effectiveness checks) in the Quality Management System. Track and trend Quality System Data. Perform Root Cause Analysis. Review of change controls for content and completeness. Generate and update standard operating procedures to define and improve quality system functions. Participate in the implementation and monitoring of the QMS training program. Interface with other departments regarding documentation requirements and complex investigations. Prepares information related to the state of the QMS to be used in routine monthly reporting and Quality Council meetings. Proactively, based on data analysis, recommends to management areas of improvement within the various operations. Participate in continuous improvement projects as required.   Minimum Requirements:  Bachelor's Degree in a relevant life science field such as Biology, Microbiology, Chemistry, Biochemistry, etc. with at least 8 years of working experience in Quality Assurance, Quality Control or Manufacturing. Previous professional experience with cGMPs and associated regulatory compliance requirements and guidelines for the manufacture, testing, and release of pharmaceutical or biopharmaceutical products. Knowledge of FDA requirements including 21CFR210, 211 and Quality System Regulations. Able to rapidly adapt to changing environment and circumstances requiring flexibility, tolerance and great sense of urgency while ensuring that all cGMP and Regulatory requirement are met. Experience in compiling data to support metrics analyzing current processes. Proficiency with Word, Excel and Power Point.   Additionally, we prefer candidate that have: The ability to effectively build and maintain relationships with multiple departments in order to effectively solve problems. The ability to lead teams and meetings and represent Quality at cross-functional meetings. Must exercise accurate judgment and be able to evaluate information critically and decide upon appropriate course of action. Must be able to correlate events and determine the action plan required to avoid incidents recurrence and or regulatory exposure. The ability to organize, prioritize and deliver tasks & projects with a sense of urgency under minimal supervision with neglecting attention to detail. The ability to enable and drive change while being focused on internal and external customers. The ability to communicate well both verbally and in writing with all levels both inside and outside of the organization. Prior experience with Lean Six Sigma. Capable to manage multiple priorities.   Novavax, Inc. is a clinical-stage biotechnology company committed to delivering novel products to prevent a broad range of infectious diseases. Using innovative proprietary recombinant nanoparticle vaccine technology, we produce vaccine candidates to efficiently and effectively respond to both known and emerging disease threats. Our vaccine candidates are genetically engineered three-dimensional nanostructures that incorporate recombinant proteins critical to disease pathogenesis. Our product pipeline targets a variety of infectious diseases, with clinical vaccine candidates for respiratory syncytial virus (RSV) and Ebola virus (EBOV), and preclinical programs for Zika virus (ZIKV), seasonal influenza and a combination respiratory vaccine candidate, as well as other infectious disease vaccine candidates. Novavax, Inc. is headquartered in Gaithersburg, Maryland with additional facilities in Rockville, Maryland and Uppsala, Sweden. Novavax is traded on the Nasdaq Stock Market under the symbol NVAX and is dedicated to developing novel vaccines to address infectious disease. Novavax, Inc. offers a base salary, annual bonus, stock options, professional career development/growth opportunities, and a comprehensive benefits package including medical, dental, vision, Rx, STD, LTD, Life, Optional Life, 401(k) plan.   Equal Opportunity Employer/Veterans/Disabled Novavax, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Aug 7th, 2018 08:47AM Aug 7th, 2018 08:47AM Health Care Pharmaceuticals & Biotechnology
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 7th, 2018 12:00AM Scientist, Analytical Development (Contract) Open Novavax CONTRACTOR Gaithersburg MD USA Jul 30th, 2018 12:00AM The candidate will work in the Characterization group support one or two projects related to RSV F or Nano HA. The candidate will work in the lab using methods such as liquid chromatography, dynamic light scattering, and analytical ultracentrifugation and will assist in various studies supporting characterization of the Nano HA and RSV F products. The candidate will organize and present data in meetings and will work closely with other members of the Characterization group. Minimum requirements: Undergraduate or graduate degree in a related field of science (e.g. chemistry, biochemistry, biophysics) At least five years of lab research experience, with supporting record of peer-reviewed publications Experience in methods for protein characterization, including HPLC separations based on size, charge, or hydrophobicity Analytical Ultracentrifugation (AUC) of biomolecules or nanoparticles Dynamic Light Scattering (DLS) of proteins or nanoparticles Proficient with Microsoft Office programs Excellent organizational, verbal, and written communication skills Detail oriented and self-motivated Aug 7th, 2018 08:47AM Aug 7th, 2018 08:47AM Health Care Pharmaceuticals & Biotechnology
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 7th, 2018 12:00AM Quality Assurance Specialist II/III, Analytical (Contract Assignment) Open Novavax CONTRACTOR Gaithersburg MD USA Aug 6th, 2018 12:00AM At Novavax, a clinical-stage vaccine company, we are creating tomorrow's vaccines today! We seek to attract, develop, and retain talented people who share our passion for science, medicine, and human health. We foster an environment of teamwork and collaboration, built on a culture that values and appreciates its employees. We are a fast-paced company that provides employees with opportunities to achieve personal and professional goals while also maintaining a balance between work and personal life. The QA Specialist, Quality Operations, is responsible for support of GMP compliance with a focus on QC/analytical areas through provision of critical review, organization, and Quality oversight of records generated during GMP release and stability testing of biotechnologically produced vaccines in a fully functional GMP manufacturing facility. This is a temporary assignment for 6+ months.   Responsibilities include but are not limited to:  Review of analytical records generated during the testing of vaccines for compliance to current Good Manufacturing Practices (cGMP) and Novavax Standard Operating Procedures (SOPs). Records include, but are not limited to: Lot release test records. Stability test records. Raw material test records. Review of records related to the general operation and upkeep of a GMP Quality Control laboratory, including but not limited to, records associated with: Preparation, qualification, and control of standards and controls. Test sample chain of custody. Preparation, qualification, and control of laboratory reagents. Provision of QA support for the stability program, including: Review and compilation of stability time point packages and reports. Review of stability information submitted in Regulatory filings. Interaction with Quality Control group to resolve review observations. Maintenance of systems for organizing, tracking, and reporting completed reviews and metrics related to the review system. Provide review and input for generation of new or revised QA SOPs and other controlled documentation. Author quality documents as assigned. Other duties as assigned.   Minimum requirements:  Bachelor's degree in a scientific discipline. Minimum 2 years work experience in Quality Assurance and/or Quality Control in a GMP regulated environment. Familiarity with biotechnological testing methodologies, including HPLC, Immunoassays (e.g. ELISA, Western Blot and SRID), SDS-PAGE, PCR. Familiarity with stability program requirements for biotech products. Proficiency with Microsoft Office and Outlook. Proficiency with Microsoft Access a plus. Excellent multi-tasking and organizational skills.   Novavax, Inc. is a clinical-stage biotechnology company committed to delivering novel products to prevent a broad range of infectious diseases. Using innovative proprietary recombinant nanoparticle vaccine technology, we produce vaccine candidates to efficiently and effectively respond to both known and emerging disease threats. Our vaccine candidates are genetically engineered three-dimensional nanostructures that incorporate recombinant proteins critical to disease pathogenesis. Our product pipeline targets a variety of infectious diseases, with clinical vaccine candidates for respiratory syncytial virus (RSV) and Ebola virus (EBOV), and preclinical programs for Zika virus (ZIKV), seasonal influenza and a combination respiratory vaccine candidate, as well as other infectious disease vaccine candidates. Novavax, Inc. is headquartered in Gaithersburg, Maryland with additional facilities in Rockville, Maryland and Uppsala, Sweden. Novavax is traded on the Nasdaq Stock Market under the symbol NVAX and is dedicated to developing novel vaccines to address infectious disease. Novavax, Inc. offers a base salary, annual bonus, stock options, professional career development/growth opportunities, and a comprehensive benefits package including medical, dental, vision, Rx, STD, LTD, Life, Optional Life, 401(k) plan.   Equal Opportunity Employer/Veterans/Disabled Novavax, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Aug 7th, 2018 08:47AM Aug 7th, 2018 08:47AM Health Care Pharmaceuticals & Biotechnology
nasdaq:nvax novavax.applicantpro.com novavax.applicantpro.com Aug 8th, 2018 12:00AM Analytical Development Associate II (Contract) Open Novavax CONTRACTOR Gaithersburg MD USA Jun 19th, 2018 12:00AM At Novavax, a clinical-stage vaccine company, we are creating tomorrow's vaccines today! We seek to attract, develop, and retain talented people who share our passion for science, medicine, and human health. We foster an environment of teamwork and collaboration, built on a culture that values and appreciates its employees. We are a fast-paced company that provides employees with opportunities to achieve personal and professional goals while also maintaining a balance between work and personal life. We are currently looking for an Analaytical Associate II to work as a part of our Molecular and Cellular Virology Group, within the Analytical Development Department. The successful candidate will report a team leader in the Molecular and Cellular Virology Group. The successful candidate will be responsible for in-process sample testing, detecting infectious, and potency assays. The candidate will make detailed observations, analyze data, and interpret results. The candidate will receive general instructions from a supervisor for routine work and new assignments                                                                                                                                  Duration: July 2018-December 2018, with possibility for extension   Minimum requirements:  BS degree in a relevant scientific discipline with 2+ years relevant industry experience MS degree in a relevant scientific discipline with 1+ years of relevant industry experience Experience recording data according to Good Documentation Practices Standards Ability to plan and perform complex procedures and experiments Experience analyzing and interpreting data Proficiency in Microsoft Word, PowerPoint, Excel Proficiency with statistical software is a plus   Novavax, Inc. is a clinical-stage biotechnology company committed to delivering novel products to prevent a broad range of infectious diseases. Using innovative proprietary recombinant nanoparticle vaccine technology, we produce vaccine candidates to efficiently and effectively respond to both known and emerging disease threats. Our vaccine candidates are genetically engineered three-dimensional nanostructures that incorporate recombinant proteins critical to disease pathogenesis. Our product pipeline targets a variety of infectious diseases, with clinical vaccine candidates for respiratory syncytial virus (RSV) and Ebola virus (EBOV), and preclinical programs for Zika virus (ZIKV), seasonal influenza and a combination respiratory vaccine candidate, as well as other infectious disease vaccine candidates. Novavax, Inc. is headquartered in Gaithersburg, Maryland with additional facilities in Rockville, Maryland and Uppsala, Sweden. Novavax is traded on the Nasdaq Stock Market under the symbol NVAX and is dedicated to developing novel vaccines to address infectious disease.   Equal Opportunity Employer/Veterans/Disabled Novavax, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Aug 8th, 2018 07:53AM Aug 8th, 2018 07:53AM Health Care Pharmaceuticals & Biotechnology

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