About this opportunity
Abbott Laboratories lists this Sr Technical Services Application Scientist opportunity in madison, Wisconsin. Review the employer’s description below for duties, qualifications and application requirements.
Job description
The Opportunity
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 115,000 colleagues serve people in more than 160 countries.
What You’ll Work On
Include, but are not limited to, the following:
Receive and document incoming customer communications.
Work cooperatively with the technical services team and internal functional departments to troubleshoot and resolve customer questions or requests related to reagents, consumables, and assay issues.
Lead troubleshooting of customer issues through root cause investigation, experiment design, study execution, data analysis, and reporting.
Conduct bench level experiments within several product areas.
Prepare technical experiment reports with all technical specifications and information to present to the supervisor or project team.
Lead development of training materials for internal and external customers and train customers.
Coordinate with the development and marketing teams for proper implementation of new products to provide technical input and participate in decisions affecting project plans and experimental design.
Prepare detailed technical protocols.
Communicate the customer feedback for product requirements to the development team for better designs and implementation of new and existing products.
Identify gaps in processes, make recommendations, and implement change.
Draft and distribute the content of customer communications, customer notifications, and technical or service bulletins.
Identify, contribute, implement, and report on improvements in processes and products.
Contribute ideas or drive improvements to team processes.
Lead complex level projects, sit on core teams, and participate with complex projects.
Develop white papers.
Direct customer interactions to problem solve and facilitate enhancement generation.
Train and mentor team members.
Summarize and document troubleshooting activities or technical summary.
Ability to communicate clearly, frequently, and accurately in person, via the telephone, or by email.
Ability to work independently.
Apply advanced analytical and troubleshooting skills.
Apply strong communication and organizational skills.
Apply high complexity problem-solving abilities to provide technical input, design experiments, propose product enhancement ideas and voice of customer (VOC).
Ability to maintain confidentiality of sensitive information.
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 on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
Ability to work on a computer and phone simultaneously.
Ability to use a telephone through a headset.
Ability to travel 35% of working time away from work location, may include overnight/weekend travel.
Required Qualifications
Bachelor’s Degree in Life Sciences or field as outlined in the essential duties.
10+ years of experience in the life sciences industry.
5+ years of experience working in a molecular diagnostic or clinical laboratory.
5+ years of experience working in next generation sequencing.
Demonstrated advanced proficiency or coursework with molecular biology techniques and Real-Time- polymerase chain reaction (PCR) Assays.
Demonstrated advanced knowledge of clinical lab regulations for computer aided planning (CAP), clinical laboratory improvement amendments (CLIA), invitro diagnostic regulation (IVDR), and food and drug administration (FDA).
Demonstrated understanding of statistical and mathematical methods in biology or genetics.
Advanced data analysis skills and analytical aptitude.
Proficiency in Microsoft Office programs, such as Word, Excel, PowerPoint, Outlook, Access, and OneNote.
Demonstrated ability to perform the essential duties of the position with or without accommodation.
Authorization to work in the United States without sponsorship.
Preferred Qualifications
7+ years of experience in a Biotech/Medical Device field working in a regulated environment, e.g., CAP, CLIA, ISO 13485, FDA GMP, or USDA.
7+ years of experience working within Quality System Regulations.
5+ year of experience working in a technical support function.
Experience working in Next Generation Sequencing (NGS).
The base pay for this position is $99,300.00 – $198,700.00. In specific locations, the pay range may vary from the range posted.
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Worksite address
madison, WI, 53774, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.