Associate Research Scientist II at Abbott

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position works out of our Madison, Wisconsin location in the Cancer Diagnostics R&D Product Development Division. The Associate Research Scientist II, with some guidance from more experienced scientists, works on projects which are moderate to complex in scope and will have the chance to work on our Multi-Cancer Early Detection Test. What You’ll Work On Support moderate to complex R&D projects by planning and executing experiments, analyzing data, and contributing to scientific problem-solving with some guidance from senior scientists. Conducts late-stage product development studies, including stability testing, design verification and validation, product performance improvements, and manufacturing investigations. Develop and applies expertise in molecular biology techniques, including blood processing, nucleic acid extraction, qPCR, protein-based assays, and next-generation sequencing (NGS) methods. Collaborate effectively within and across functional teams in a fast-paced, milestone-driven environment to support the development and continuous improvement of early cancer detection diagnostics while maintaining high quality standards. Essential Duties include but are not limited to the following: Conduct bench level experiments within a specific product or technology area and identifies problems and discrepancies. With some guidance, plan and analyze results of bench level experiments within a specific product or technology area. Operate scientific instrumentation related to performance of duties and notify appropriate personnel of any problems. Effectively utilize and apply methods or technologies and provide ideas for new techniques, when appropriate. Maintain knowledge of technological industry developments that could assist in completion of an assignment or aid in the development of new processes or procedures. Provide technical input and participates in decisions affecting project planning and experimental design. Prepare and provide information and generate data for scientific abstracts/conferences/project meetings/publications. Follow research plans and experimental outlines to write experimental protocols and perform laboratory experiments. Maintain lab notebook in a complete and consistent manner, following all legal, ISO, and QSR requirements, as well as keeping clear and complete. Prepare reports and documentation providing the analysis or summarization of experimental results and outcomes to supervisor, technical teams/groups, or project teams. Present experimental results, scientific ideas and findings, information, and updates at project or departmental meetings. Present clear project summaries and outcomes in written and verbal formats to supervisor and other members of the scientific team. Work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. Work on individual assignments and with project team members, as appropriate, to meet department and project objectives. Work within project timeframes that are established collaboratively by team members. Exercise discretion and independent judgement to interpret results, analyze data, and present findings in a professional and knowledgeable manner. Ability to train and mentor junior level research associates. Ability to organize, present, and convey moderate problems or issues. Ability to communicate clearly with supervisor and group members. Excellent presentation skills. Ability to collaborate and work effectively within team and department. Strong attention to detail skills. Ability to effectively work on several varied projects at one time, with frequent changing priorities. Successful in analytical, problem solving, and decision-making skills. Successful in technical proficiency, scientific creativity, collaboration with others, and independent thought. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company’s Quality Management System policies and procedures. Regular and reliable attendance. Ability to work nights and/or weekends, as needed. Ability to lift to 20 pounds for approximately 5% of a typical working day. Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 50% of a typical working day. Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height. Ability to comply with any applicable personal protective equipment requirements. Ability to use various types of laboratory equipment including microscopes, microtomes, blades, strainers, pipettes for extended periods of time. May perform repetitious actions using lab tools. Ability to use near vision to view samples at close range. May be exposed to hazardous materials, tissue specimens and instruments with moving parts, lasers, heating and freezing elements, and high-speed centrifugation. Ability and means to travel between Exact Sciences locations. Ability to travel 5% of working time away from work location, may include overnight/weekend travel. Minimum Qualifications Bachelor’s degree in Life Sciences, Medical Technology, Clinical Laboratory Science, Chemical/Physical/Biological Science, or related field. 3 years of relevant experience. 2 years of hands-on experience in molecular biology and /or biochemical techniques. Basic understanding of GMP, ISO, and Quality Systems. Demonstrated ability to apply statistical and mathematical methods in biology/genetics/genomics. Proficient in Microsoft Office Word, Excel, and PowerPoint. Authorization to work in the United States without sponsorship. Demonstrated ability to perform the Essential Duties of the position with or without accommodation. Preferred Qualifications M.S. degree in Molecular Biology, Biochemistry, Genetics, Biomedical Engineering, Computational Biology, or related scientific discipline. 4 years of experience supporting development, optimization, validation, or transfer of molecular diagnostic assays in a regulated environment. Experience with nucleic acid technologies including qPCR, multiplex PCR, next-generation sequencing (NGS), DNA/RNA extraction, hybridization-based methods, or related molecular biology techniques. Working knowledge of Design Control, Verification & Validation (V&V), Method Validation, Measurement System Analysis (MSA), and scientific risk assessment methodologies. Experience designing and executing statistically sound experiments, including Design of Experiments (DOE), precision studies, robustness studies, capability assessments, or threshold-setting activities. Proficiency analyzing scientific data using JMP, R, Python, or equivalent statistical software. Experience generating, reviewing, and maintaining technical documentation within a Quality Management System, including protocols, reports, test methods, requirements, design documentation, change controls, and risk assessments. Familiarity with GMP, GLP, ISO 13485, FDA Quality System Regulation (QSR), and/or Design Control requirements for in vitro diagnostic (IVD) products. Experience supporting reagent, control, calibrator, or consumable development, characterization, release testing, or lifecycle management. Demonstrated ability to independently troubleshoot complex experimental issues and identify root causes using data-driven approaches. Experience collaborating across multidisciplinary teams including R&D, Product Development, IT, Quality, Regulatory Affairs, Manufacturing, and Operations. Experience presenting experimental results and technical recommendations to technical teams, project teams, and leadership audiences. Knowledge of bioinformatics, genomics, cancer biology, or liquid biopsy technologies. Experience with laboratory automation, high-throughput workflows, or development of scalable laboratory processes. Proven ability to manage multiple projects simultaneously while meeting project timelines and quality requirements. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at abbott.com , on LinkedIn at linkedin.com , and on Facebook at facebook.com . The base pay for this position is $61,300.00 – $122,700.00 In specific locations, the pay range may vary from the range posted. JOB FAMILY: Research and Discovery DIVISION: ONCO Cancer Diagnostics LOCATION: United States > Madison : 501 Charmany Dr ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 5 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Work with human blood or other potentially infectious materials Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law link - English: webstorage.abbott.com EEO is the Law link - Espanol: webstorage.abbott.com

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Must-haves

JOB DESCRIPTION: Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:
Career development with an international company where you can grow the career you dream of.
An excellent retirement savings plan with a high employer contribution.
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
This position works out of our Madison, Wisconsin location in the Cancer Diagnostics R&D Product Development Division.
What You’ll Work On
Support moderate to complex R&D projects by planning and executing experiments, analyzing data, and contributing to scientific problem-solving with some guidance from senior scientists.
Conducts late-stage product development studies, including stability testing, design verification and validation, product performance improvements, and manufacturing investigations.
Develop and applies expertise in molecular biology techniques, including blood processing, nucleic acid extraction, qPCR, protein-based assays, and next-generation sequencing (NGS) methods.
include but are not limited to the following:
Conduct bench level experiments within a specific product or technology area and identifies problems and discrepancies.

Nice-to-haves

M.S. degree in Molecular Biology, Biochemistry, Genetics, Biomedical Engineering, Computational Biology, or related scientific discipline.
Experience with nucleic acid technologies including qPCR, multiplex PCR, next-generation sequencing (NGS), DNA/RNA extraction, hybridization-based methods, or related molecular biology techniques.
Working knowledge of Design Control, Verification & Validation (V&V), Method Validation, Measurement System Analysis (MSA), and scientific risk assessment methodologies.
Experience designing and executing statistically sound experiments, including Design of Experiments (DOE), precision studies, robustness studies, capability assessments, or threshold-setting activities.
Proficiency analyzing scientific data using JMP, R, Python, or equivalent statistical software.
Familiarity with GMP, GLP, ISO 13485, FDA Quality System Regulation (QSR), and/or Design Control requirements for in vitro diagnostic (IVD) products.
Experience supporting reagent, control, calibrator, or consumable development, characterization, release testing, or lifecycle management.
Demonstrated ability to independently troubleshoot complex experimental issues and identify root causes using data-driven approaches.
Experience collaborating across multidisciplinary teams including R&D, Product Development, IT, Quality, Regulatory Affairs, Manufacturing, and Operations.
Experience presenting experimental results and technical recommendations to technical teams, project teams, and leadership audiences.

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Platform: workday
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