Scientist, Associate
1 week ago
**About Abbott**
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
- Career development with an international company where you can grow the career you dream of.
- A company recognized as a great place to work in dozens of countries around the world 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 a best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
This position works out of our Ottawa, Ontario location in the Point of Care, Diagnostics division. We’re empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people.
Our Point of Care diagnostic portfolio spans key health and therapeutic areas, including infectious disease, cardiometabolic, informatics and toxicology.
As an Associate Scientist, and a member of our Bioreagents team, you will contribute to the team’s success by supporting continuity of supply efforts for bioreagents accepted materials and manufactured biochemical solutions by performing material qualifications for new vendor lots of incoming materials and completing work packages to update material specifications documentation when suppliers change product specifications and/or obsolete part numbers.
**What You’ll Do**
- Assist with material management and continuity of supply for bioreagents accepted materials by i) performing verification-based material qualifications for new vendor lots of materials and ii) completing work packages to update material specification documentation when there are supply disruptions caused by vendor changes to product specifications and/or obsoleted part numbers.
- Develop efficient execution strategies for complex tasks, communicate clearly and build team consensus.
- Coordinate experiments and verification activities with Engineering support, QA, operations, procurement, and planning staff.
- Responsible for utilizing statistical methods and statistical analyses in verification protocols and reports; and can draw conclusions from data analysis.
- Prioritize problems and participate in investigations and root cause analysis to identify sources of variability impacting product performance, when implementing different vendor lots of bioreagents accepted materials or newly made reagents.
- Communicate ideas and suggestions for improving processes; actively participate in implementing solutions.
- Manage documentation updates through the Design Control System by drafting document updates and driving approvals in the electronic document system.
- Ensures process changes and improvements are validated, verified, and justified appropriately according to established standards and procedures.
- Work independently in accordance with standard practices, policies, and precedents; seek direction when needed.
- Maintain contact with managers and group members from related functional areas, including product engineering, manufacturing, quality assurance and test.
- Understand and comply with Quality and EH&S policies, procedures, and guidelines. Safeguard the environment and facilitate a safe and healthy workplace culture.
- Communicate effectively orally and in writing with planning, operators, equipment technologists and group members of related areas and managers.
- Flexibility to support other miscellaneous duties and business demands as required.
**Required Qualifications**
- A Bachelor’s Degree in Science or Engineering with Chemical, Biochemical or Mechanical Engineering focus, or equivalent.
- 1 or more years related work experience preferred in a manufacturing/laboratory environment.
- Knowledge of MS Office, SAS JMP, Minitab
- Ability to design and conduct experiments, analyze and interpret data and document conclusions with appropriate attention to detail; experience using statistical methods is an asset.
- Analytical skills, creativity and innovative approach to problem solving.
- Ability to determine required analysis to make practical, objective decisions about the best solutions to problems.
- Effective at planning and coordinating, with excellent time-management skills.
- Experience in writing reports and quality records.
- Enthusiasm and propensity to continuous learning and experimentation.
- Ability to build and use an effective network of people inside and/or outside the organization to give and receive information and to accomplish work objectives.
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