IVD Assay Scientist: FDA/ISO & Reagent Development

Integrated Resources Inc.; San Jose (CA); On-site; USD 90,000 - 140,000; Full time

Job summary

Integrated Resources, Inc. in the San Jose area is seeking a candidate with 3 years of industry experience in FDA or ISO environments and 2 years of assay development to advance our IVD reagent programs.

The role focuses on assessing feasibility and development of new IVD reagents, working with cross‑functional teams to ensure regulatory compliance and reliable performance in clinical settings. Strong collaboration and meticulous execution are essential.

Qualifications

• 3 years industry experience in FDA or ISO environment.
• 2 years assay development
• Assessing feasibility and development of new IVD reagents.

Skills

FDA/ISO experience

Assay development

IVD reagents development

Job description

IRI believes in commitment, Integrity and strategic workforce solutions.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

We’ve stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.

Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients’ success.

Job Description

• 3 years industry experience in FDA or ISO environment.
• 2 years assay development
• Assessing feasibility and development of new IVD reagents.