Technician III-Medtronic,USA

We believe that when people from different cultures, genders, and points of view come together, innovation is the result —and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive. In general, the following responsibilities apply for the Lab Technician III role. This includes, but is not limited to, the following

Skills

• Develops, validates, and maintains quality data queries and reports
• Partners with cross-functional teams to analyze quality data signals and completes relevant quality system documentation
• Performs a variety of technical procedures such as preparing routine solutions and reagents and performing routine reactions.
• Makes and records observations; performs simple calculations; and collects and prepares data for evaluation.
• Conducts laboratory support functions such as stocking and distributing supplies and equipment; arranging and dismantling apparatus; and collecting, washing, and storing glassware.
• Performs technical and record keeping duties in conformance with company and regulatory policies and standards to meet quality and accuracy requirements.
• May analyze compounds and manage corporate compound collection.
  Performs technical procedures in one or more of the following areas: Production, Research and
• Development, Quality Control/Assurance, and/or Compliance/Environmental
• Compiles, analyzes, and presents periodic quality data analysis, including Periodic Safety Update
• Reports (PSUR) for required regulatory submissions, and quarterly Product Quality Meeting data.
• Travel requirement: 0%

Qualifications

• TO BE CONSIDERED FOR THIS ROLE, PLEASE BE SURE THE MINIMUM REQUIREMENTS ARE EVIDENT ON YOUR RESUME
• High School diploma, vocational or technical education
  Minimum of 4 years of work experience in Data Analysis OR Advanced degree in technical discipline with 0+ years of work experience.
  Nice to Have
• Strong analytical skills and experience with large, complex datasets
• Report validation experience
• Strong written and verbal communication skills and work cooperatively as part of a team and cross functionally
• Ability to manage project timelines to execute deliverables in a timely manner.
• Ability to solve problems and innovate solutions.
• Medical Device Industry experience.
• Quality experience working in a regulated industry.
• Knowledge of Microsoft Office Applications (Word, Excel, Access, and PowerPoint) and Windows OS.
• Familiarity with these regulations: FDA 21 CFR Part 820 cGMP, ISO 13485, ISO 10012, and ISO 17025.
• Experience with and passion for Continuous Improvement