Miltenyi Biotec
Overview
Your Role: This position is primarily responsible for performance of duties within the functional area of molecular engineering of gene vectors and immune or stem cells. Responsibilities
Responsible for the analysis of lentiviral vector function using standard assays, monitoring the impact of cell engineering with LV that leads to new functional activities of those cells, understanding the impact of LV transduction on the biology of immune effector cells, stem cells, and immortalized cell lines. Responsible for culture and analysis of primary human T cell lines, immortalized cell lines, cryopreservation of these lines, and documentation of cell line identity. Perform analytical assays such as, qPCR, SDS-page, Western Blot, protein and DNA quantitation, Flow Cytometry/FACS. Assist with the generation of LV laboratory stocks for specific cell biology projects. Design of specific experiments to test LV function, appropriate statistical analysis of results, ability to communicate results internally, for publication, and in scientific meetings. The ability to generate LV-based gene vectors as both laboratory stocks for specific research projects and in collaboration with other members of the organization desiring to implement their use. Ability to design and execute animal experiments to test immune effector cell function, or the function of modified stem cells, in model systems of human disease. Design and develop new processes and protocols, as needed. Maintain inventory and restock supplies when needed. Complete Purchase Order Requests. Responsible for cleaning of equipment and work areas as required. Qualifications
PH.D. or master’s degree (M.S.) in Molecular Biology, Immunology, or Virology with at least one-year related experience and/or training; or equivalent combination of education and experience. Compensation and Benefits
The hiring range for this position is expected to fall between $107,800-$117,300/year, reflecting the range candidates can reasonably expect to be considered for at time of offer, based on factors such as experience, internal equity, and qualifications. The salary of the finalist(s) selected for this role will be set based on a variety of considerations, including but not limited to internal equity, experience, education, specialization, skills, abilities, and training. The above range represents the Company’s good faith and reasonable estimate of possible compensation at the time of posting. In addition to your salary, the Company offers a comprehensive benefits package, including health, vision, and dental insurance, as well as a 401(k) plan. All benefits are subject to eligibility requirements. Certain positions may also be eligible for additional compensation such as bonuses or commissions. Miltenyi Biotec is an EO Employer – M/F/Veteran/Disability/Sexual Orientation/Gender Identity. Miltenyi Biotec, Inc. participates in E-Verify. About Miltenyi Biotec
Are you ready to start revolutionizing biomedical research? When you join Miltenyi Biotec, you join a family that is passionate about making a real impact – one breakthrough at a time. One integral division of that Miltenyi Biotec family is Miltenyi Bioindustry— our contract development and manufacturing organization (CDMO). As a full-scale CDMO, we provide customers with services for the development and manufacturing of lentiviral vectors and cell and gene therapy products. Miltenyi Bioindustry plays a unique role as both the producer and the service provider, relying on our instruments and reagents for each workflow step, controlling the entire supply chain and thus delivering greater security and planning clarity to our customers. Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
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Your Role: This position is primarily responsible for performance of duties within the functional area of molecular engineering of gene vectors and immune or stem cells. Responsibilities
Responsible for the analysis of lentiviral vector function using standard assays, monitoring the impact of cell engineering with LV that leads to new functional activities of those cells, understanding the impact of LV transduction on the biology of immune effector cells, stem cells, and immortalized cell lines. Responsible for culture and analysis of primary human T cell lines, immortalized cell lines, cryopreservation of these lines, and documentation of cell line identity. Perform analytical assays such as, qPCR, SDS-page, Western Blot, protein and DNA quantitation, Flow Cytometry/FACS. Assist with the generation of LV laboratory stocks for specific cell biology projects. Design of specific experiments to test LV function, appropriate statistical analysis of results, ability to communicate results internally, for publication, and in scientific meetings. The ability to generate LV-based gene vectors as both laboratory stocks for specific research projects and in collaboration with other members of the organization desiring to implement their use. Ability to design and execute animal experiments to test immune effector cell function, or the function of modified stem cells, in model systems of human disease. Design and develop new processes and protocols, as needed. Maintain inventory and restock supplies when needed. Complete Purchase Order Requests. Responsible for cleaning of equipment and work areas as required. Qualifications
PH.D. or master’s degree (M.S.) in Molecular Biology, Immunology, or Virology with at least one-year related experience and/or training; or equivalent combination of education and experience. Compensation and Benefits
The hiring range for this position is expected to fall between $107,800-$117,300/year, reflecting the range candidates can reasonably expect to be considered for at time of offer, based on factors such as experience, internal equity, and qualifications. The salary of the finalist(s) selected for this role will be set based on a variety of considerations, including but not limited to internal equity, experience, education, specialization, skills, abilities, and training. The above range represents the Company’s good faith and reasonable estimate of possible compensation at the time of posting. In addition to your salary, the Company offers a comprehensive benefits package, including health, vision, and dental insurance, as well as a 401(k) plan. All benefits are subject to eligibility requirements. Certain positions may also be eligible for additional compensation such as bonuses or commissions. Miltenyi Biotec is an EO Employer – M/F/Veteran/Disability/Sexual Orientation/Gender Identity. Miltenyi Biotec, Inc. participates in E-Verify. About Miltenyi Biotec
Are you ready to start revolutionizing biomedical research? When you join Miltenyi Biotec, you join a family that is passionate about making a real impact – one breakthrough at a time. One integral division of that Miltenyi Biotec family is Miltenyi Bioindustry— our contract development and manufacturing organization (CDMO). As a full-scale CDMO, we provide customers with services for the development and manufacturing of lentiviral vectors and cell and gene therapy products. Miltenyi Bioindustry plays a unique role as both the producer and the service provider, relying on our instruments and reagents for each workflow step, controlling the entire supply chain and thus delivering greater security and planning clarity to our customers. Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
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