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Product Support Scientist; Fluids

Job in City of Rochester, Rochester, Monroe County, New York, 14602, USA
Listing for: The Fountain Group
Full Time position
Listed on 2026-02-08
Job specializations:
  • Healthcare
    Medical Technologist & Lab Technician, Medical Science, Clinical Research
Salary/Wage Range or Industry Benchmark: 35 - 45 USD Hourly USD 35.00 45.00 HOUR
Job Description & How to Apply Below
Position: Product Support Scientist (Fluids)
Location: City of Rochester

Overview

The Fountain Group is currently seeking a Product Support Scientist (Fluids) for a prominent client of ours. This position is located at Rochester, NY. Details for the position are as follows:

  • Title:

    Product Support Scientist (Fluids)
  • Location:

    Rochester, NY
  • Duration: 1 Year (With Possible Extension/Hire)
  • Pay range: $35-45/Hour on W2

This is a contract position in the Operations Product Support team at Quidel Ortho, located in Rochester, NY. This role supports validation activities for new products within a medical device manufacturing facility and requires the ability to work both independently and as part of a cross-functional team.

Responsibilities
  • Support validation work for new products, including laboratory testing utilizing VITROS analyzers.
  • Prepare and handle clinical test specimens according to approved procedures, best practices, and safety requirements, including appropriate PPE.
  • Perform pilot-scale formulations with biological materials, as needed.
  • Operate and maintain laboratory equipment; complete all required documentation in real time (QC records, instrument logs, test records).
  • Independently execute laboratory experiments and assist with troubleshooting instrument and test failures, as needed.
  • Review and analyze data; document conclusions and test summaries in appropriate quality records within Quidel Ortho's quality system.
  • Ensure organization, documentation, and tracking of long-term studies with multiple factors, products, and conditions.
  • Maintain a working knowledge of cGMP requirements and adhere to all quality, regulatory, and safety guidelines.
  • This role involves both laboratory and computer-based work.
Qualifications
  • Bachelor s degree in a scientific field (e.g., Chemistry, Biology, or equivalent) required.
  • Experience in an FDA-regulated industry and in validation for medical devices preferred.
  • Familiarity with VITROS products and VITROS analyzers highly desired.
  • Familiarity with biological formulations and processing techniques highly desired.
  • Strong written and verbal communication skills with excellent attention to detail required.
  • Strong organizational skills and ability to manage complex, long-term studies required.
  • Proficiency in Excel required, with additional statistical analysis skills preferred.

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