AskBio Inc. a wholly owned and independently operated subsidiary of Bayer AG is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular central nervous system cardiovascular and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure limb-girdle muscular dystrophy multiple system atrophy Parkinsons disease and Pompe disease. AskBios gene therapy platform includes Pro10 an industry-leading proprietary cell line manufacturing process and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park North Carolina and European headquarters in Edinburgh Scotland the company has generated hundreds of proprietary capsids and promoters several of which have entered pre-clinical and clinical testing.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform peoples lives.
Our principles:
Advance innovative science by pushing boundaries.
Bring transformative therapeutics to patients in need.
Provide an environment for employees to reach their fullest potential.
Our values:
Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
Cultivate Collaboration. Strive to be the best teammate actively listen openly communicate and embrace diverse points of view.
Embrace Responsibility. We are humbled by the enormity of our hold a relentless commitment to advance science and clinical outcomes for our patients families and caregivers.
Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
Act with Uncompromising Integrity. Be honest transparent and committed to doing whats right in every situation. Make clear commitments and follow through.
The Research Associate II Bioanalytical will report to the Director Translational Biomarkers and will participate in the development qualification validation and execution of assays investigating biodistribution viral shedding and functional assessments in support of pre-clinical and clinical stage programs. This is an on-site lab-based position in Morrisville NC and prior experience with methods for extraction and quantification of nucleic material (DNA RNA) and protein is required. The ideal candidate would have knowledge of various molecular techniques to quantify transgene expression. Candidates may also have opportunities to learn different techniques for protein assessment. Experience with GxP regulation and working in a regulated lab space is preferred but not required.
Job Responsibilities
Isolate and quantify nucleic acids and proteins from various model systems and tissue types
Participate in assay design including assay qualification and validation
Utilize molecular techniques including but not limited to gene expression analysis primer probe set design/validation ddPCR RT-ddPCR ELISA western blots and MSD for sample analysis
Responsible for co-authoring and reviewing test methods work plans SOPs and qualification/validation reports
Contribute to data review and quality control of data in support of regulatory filings
Perform routine instrument maintenance and performance verification
Maintain organized electronic and/or paper-based documentation that is fit-for-purpose with regards to regulatory requirements.
Receive accession and manage samples using LIMS
Perform data analysis and effectively communicate results in formal reports and presentations for technical discussions
Maintain inventories and/or place orders of reagents and materials needed for the assigned projects allowing for timely execution of related lab work
Ensure lab areas are clean and organized and that equipment supplies and raw materials are available for use
Minimum Requirements
Masters degree in biology chemistry or related field OR bachelors degree in biology chemistry or related field with 2 years relevant work experience OR High School Diploma and 6 years relevant work experience
Hands-on experience with the processing of and isolation of nucleic acids and protein from material acquired from different species and organ types
Demonstrated understanding of assay qualification and/or validation requirements
Possess knowledge of and experience with multiple assays including: ddPCR RT-ddPCR ELISA western blots and/or MSD-based platforms
Excellent technical lab skills with attention to detail and the ability to assume independent ownership of workflows
Knowledge of GxP regulatory requirements
Ability to multitask among multiple projects and teams and work in a fast-paced highly interactive environment
Self-motivated organized and capable of troubleshooting independently
Proficiency in Microsoft Office Suite (Word Excel PowerPoint)
Excellent communication skills with ability to collaborate with colleagues across multiple communication platforms including e-mail Microsoft Teams and Sharepoint sites
Preferred Education Experience and Skills
Hands-on experience with assay qualification and validation
Prior work in a regulated lab environment
Familiarity with software such as Softmax Pro graphpad prism and smartsheet
Prior use of LIMS sample management software and/or lab automation
Relevant knowledge and industrial experience with gene therapy including AAV and/or lentiviral-based platforms
AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race color religion gender sexual orientation gender identity national origin age disability veteran status or any other protected status prohibited under Federal State or local laws. All employment decisions are based on valid jobrelated requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website you may request a reasonable accommodation to express interest in a specific opening by calling us at or sending us an email at .
Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio through any medium will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio no fee or payment of any kind will be paid to the agency.
Required Experience:
IC
AskBio Inc. a wholly owned and independently operated subsidiary of Bayer AG is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular central nervous system card...
AskBio Inc. a wholly owned and independently operated subsidiary of Bayer AG is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular central nervous system cardiovascular and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure limb-girdle muscular dystrophy multiple system atrophy Parkinsons disease and Pompe disease. AskBios gene therapy platform includes Pro10 an industry-leading proprietary cell line manufacturing process and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park North Carolina and European headquarters in Edinburgh Scotland the company has generated hundreds of proprietary capsids and promoters several of which have entered pre-clinical and clinical testing.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform peoples lives.
Our principles:
Advance innovative science by pushing boundaries.
Bring transformative therapeutics to patients in need.
Provide an environment for employees to reach their fullest potential.
Our values:
Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
Cultivate Collaboration. Strive to be the best teammate actively listen openly communicate and embrace diverse points of view.
Embrace Responsibility. We are humbled by the enormity of our hold a relentless commitment to advance science and clinical outcomes for our patients families and caregivers.
Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
Act with Uncompromising Integrity. Be honest transparent and committed to doing whats right in every situation. Make clear commitments and follow through.
The Research Associate II Bioanalytical will report to the Director Translational Biomarkers and will participate in the development qualification validation and execution of assays investigating biodistribution viral shedding and functional assessments in support of pre-clinical and clinical stage programs. This is an on-site lab-based position in Morrisville NC and prior experience with methods for extraction and quantification of nucleic material (DNA RNA) and protein is required. The ideal candidate would have knowledge of various molecular techniques to quantify transgene expression. Candidates may also have opportunities to learn different techniques for protein assessment. Experience with GxP regulation and working in a regulated lab space is preferred but not required.
Job Responsibilities
Isolate and quantify nucleic acids and proteins from various model systems and tissue types
Participate in assay design including assay qualification and validation
Utilize molecular techniques including but not limited to gene expression analysis primer probe set design/validation ddPCR RT-ddPCR ELISA western blots and MSD for sample analysis
Responsible for co-authoring and reviewing test methods work plans SOPs and qualification/validation reports
Contribute to data review and quality control of data in support of regulatory filings
Perform routine instrument maintenance and performance verification
Maintain organized electronic and/or paper-based documentation that is fit-for-purpose with regards to regulatory requirements.
Receive accession and manage samples using LIMS
Perform data analysis and effectively communicate results in formal reports and presentations for technical discussions
Maintain inventories and/or place orders of reagents and materials needed for the assigned projects allowing for timely execution of related lab work
Ensure lab areas are clean and organized and that equipment supplies and raw materials are available for use
Minimum Requirements
Masters degree in biology chemistry or related field OR bachelors degree in biology chemistry or related field with 2 years relevant work experience OR High School Diploma and 6 years relevant work experience
Hands-on experience with the processing of and isolation of nucleic acids and protein from material acquired from different species and organ types
Demonstrated understanding of assay qualification and/or validation requirements
Possess knowledge of and experience with multiple assays including: ddPCR RT-ddPCR ELISA western blots and/or MSD-based platforms
Excellent technical lab skills with attention to detail and the ability to assume independent ownership of workflows
Knowledge of GxP regulatory requirements
Ability to multitask among multiple projects and teams and work in a fast-paced highly interactive environment
Self-motivated organized and capable of troubleshooting independently
Proficiency in Microsoft Office Suite (Word Excel PowerPoint)
Excellent communication skills with ability to collaborate with colleagues across multiple communication platforms including e-mail Microsoft Teams and Sharepoint sites
Preferred Education Experience and Skills
Hands-on experience with assay qualification and validation
Prior work in a regulated lab environment
Familiarity with software such as Softmax Pro graphpad prism and smartsheet
Prior use of LIMS sample management software and/or lab automation
Relevant knowledge and industrial experience with gene therapy including AAV and/or lentiviral-based platforms
AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race color religion gender sexual orientation gender identity national origin age disability veteran status or any other protected status prohibited under Federal State or local laws. All employment decisions are based on valid jobrelated requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website you may request a reasonable accommodation to express interest in a specific opening by calling us at or sending us an email at .
Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio through any medium will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio no fee or payment of any kind will be paid to the agency.
Required Experience:
IC
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