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Global Technical Support Specialist

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Location: Saint Louis, United States
Position Type: Unfixed Term
Job Function: Customer Service

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.

A world leader in the field of in vitro diagnostics for over 55 years, bioMérieux provides diagnostic solutions that detect disease and contamination to improve patient health and ensure consumer safety. In North America we have more than 5,000 team members across 12 sites or subsidiaries, including Salt Lake City based BioFire Diagnostics. We believe in the power of diagnostics and bioMérieux sponsors public health initiatives and partnerships to address antimicrobial resistance, sepsis awareness, food safety, and consumer health across the globe. Come be a part of our mission to help save lives.


Position Summary:

Within the Global Industry Customer Service (GiCS), the Global Investigation Leader is responsible of Complaint Handling Process. It includes the management, the coordination and the accountability of the end to end investigation. This role, will also enable the person to represent pharmaceutical customer voice through transversal activities with other internal departments (manufacturing, R&D, marketing…).



  • Provide technical support to subsidiaries and distributors on two specific ranges intended for Industry Pharma Customers : VITEK 2 Compact and BACT/ALERT.
    • Application point of view
    • Instrument point of view
    • Software point of view
  • Be responsible and lead the investigations of concerned range of products
  • Improve investigation processes with Quality Sites based in US thanks to a global view of the systems
  • Lead the implementation of new processes and tools
  • Coordinate with various cross-functional teams within the organization including QA, QC, Manufacturing, Logistics and R&D to investigate incoming enquiries.
  • Track/report the status of investigations and escalate concerns to management in a timely manner and make decision/action plans for resolution.
  • Be THE referent in case of audit and lead the audit preparation – 1st line of contact in case of audit.
  • Perform complaint trend analysis and prepare reports for other departments.
  • Coach subsidiaries/distributors on support desks activities and troubleshoot at customer sites or remotely if necessary.
  • Develop and adapt the support tools for subs and distributors to use in the support of customers (troubleshooting, guide, FAQ, KPI, Trend analysis, training materials and customer documentation…)
  • Provide feedback on product/service issues to R&D, manufacturing and the PMO team
  • Contribute to the design of support tools for subs/distributors to use in the support of customers (troubleshooting, guide, FAQ…).
  • Be qualified as a Customer Service technical representative and Scientific referent


Studies and Experience:

  • Master degree in Microbiology required with 3 years industry experience
  • Ideally, experience in participating to regulatory audits (ex: FDA, ISO, OSHA, EPA etc.)


Skills and Qualifications:

  • First experience in the pharmaceutical market
  • Technical knowledge on VITEK 2 Compact or BACT/ALERT preferred
  • Have a system view approach : rather application specialist profile but with technical skills, taste for instrument handling, IT aspects…
  • You are recognized for your strong leadership, and your ability to convince and gain buy-in.
  • Good communication skills, good team spirit, analysis and synthesis
  • Committed to customer and to service with a sense of urgency and accountability.
  • Knowledge in ERP functioning and reporting tools (SAP, CRM…)
  • Must be proficient in Microsoft Office tools
  • Must possess good technical writing skills for drafting  investigation reports and other communications
  • High sense of autonomy and interdependence
  • Cross cultural flexibility.
  • French language is a plus


Joining bioMérieux, is choosing to join an innovative company with a long term vision, committed to the service of public health and carried out with a humanistic corporate culture. Our Group offers numerous possibilities: so come and join the 13,000 bioMérieux team members who already identify with these values!

bioMérieux is an Equal Opportunity, Affirmative Action Employer. M/F/Vet/Disability/Sexual Orientation/Gender Identity/GINA.

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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