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Reagent Manufacturing Project Manager

Location: Salt Lake City, UT, United States
Position Type: All
Job Function: Manufacturing

A family-owned company, bioMérieux has grown to become a world leader in the field of in vitro diagnostics. For almost 60 years and across the world, we have imagined and developed innovative diagnostics solutions to improve public health. Today, our teams are spread across 44 countries and serve 160 countries with the support of a large distribution network. This includes our SLC site, formerly known as BioFire Diagnostics.

Description

Responsibilities:

  • Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics’ Quality System.
  • Leads and monitors projects throughout development, initiation, planning, execution, control and closing. 
  • Acts as the point of contact and expert for assigned projects.
  • Develop risk assessment, specifications, validation plans, protocols and reports that support the qualification and validation of manufacturing processes.
  • Develop and maintain accurate timelines for multiple projects.
  • Plan and oversee the implementation of new and/or improved manufacturing processes and equipment
  • Schedule meetings, create agendas, documents meeting minutes, correspondence, and presentations
  • Communicates, prepares and presents reports, summaries and analysis to support the project and status of projects. 
  • Creates and maintains relevant project documentation throughout the project.
  • Applies project management best practices throughout the project lifecycle
  • Investigates, creates, and develops new methods and technologies for project advancement.
  • Uses professional concepts in accordance with company objectives to solve complex problems in creative and effective ways.
  • Promote QSR and regulatory compliance into assigned projects.

 

Studies and Experience:

  • Minimum of Bachelor’s degree in related scientific or engineering field.
  • Minimum two years in project management is desired.

 

Skills and Qualifications:

  • Knowledge of validation strategies as they pertain to the medical device manufacturing industry
  • Ability to relate with people at all levels within an organization
  • Must work well independently as well as in a team environment
  • Must be an effective communicator
  • Must be able to work on multiple projects simultaneously
 

BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant’s identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).

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