Associate Product Support Scientist

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.

Location:

Onsite
- Position is based in Madison, WI.

Hours:

1st shift, 8am-4:30pm.

• Provide technical and product support to Operations working cross-functionally with the Production, QC, Supply Chain, R&D, and Quality teams.
• Perform investigative testing for Out of Specification events (OOS), non-conformances (NCMRs), and corrective action preventive action (CAPA) plans through root cause investigation, experiment design, study execution, data analysis, and reporting.
• Provide support for PCR-based and/or NGS-based reagents and products.
• Provide support to Operations teams for qualifying new raw materials and alternative supply channels for products.
• Demonstrated proficiency in a variety of basic laboratory skills and techniques.
• Basic knowledge base in Molecular Biology, Biochemistry, Biotechnology, Chemistry, or a related field.
• Good understanding of in-vitro diagnostic product manufacturing processes and relevant assays (e.g. biochemical, RT-PCR, and NGS).
• Program, operate, and troubleshoot complex instrumentation such as microplate readers, real-time and digital polymerase chain reaction (PCR) instruments, next-generation sequencers, and liquid handling automation.
• Assist development and characterization of simple manufacturing processes incorporating industry standard techniques.
• Assist characterization of basic assay variability for simple measurement systems.
• Apply basic statistical techniques: assessing data normality, control charting and data trending, hypothesis testing, assessing variation, linear regression and model fitting.
• Analyze data to identify trends, assists troubleshooting and root cause investigation efforts with ability to utilize recognized root cause analysis tools.
• Assist investigations into analytical and functional assays, associated equipment, materials, and/or processes.
• Clearly and accurately generate experimental protocols, draft work instruction procedures, test methods, and summarize development activities through technical summary reports.
• Support Process and Test Method Validation readiness and execution.
• Provide support and review in generating Validation documentation.
• Write new and edit existing Quality System documents (e.g. work instructions, standard operating procedures).
• Responsible for generating/driving corrective actions/action plans for changes.
• Collaborate with other departments (Quality Engineering, R&D, Regulatory Affairs, Supply Chain, Production, Validation, Quality Control) to achieve business results.
• Able to meet objectives without negatively impacting other functions.
• Actively participates in project execution.
• Consistently hit deliverables as outlined by manager.
• Function independently with limited guidance from supervisor as well as part of a team.
• Adaptable to rapid changes in priorities, strong sense of urgency, and able to identify ways to work together to achieve results needed for all requests.
• Strong verbal and written communication skills.
• 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.
• Maintain regular and reliable attendance.
• Ability to act with an inclusion mindset and model these behaviors for the organization.
• Ability to work designated schedule.
• Ability to work nights and/or weekends, as needed.
• Ability to work on a mobile…