Posted:
8/18/2026, 8:05:31 PM
Location(s):
Dodoma Region, Tanzania ⋅ Bengaluru, Karnataka, India ⋅ Manyata, Dodoma Region, Tanzania ⋅ Karnataka, India
Experience Level(s):
Junior
Field(s):
Customer Success & Support
Workplace Type:
On-site
Position Summary:
In this cross functional Quality role, the Product Complaint Analyst 2 will be responsible for processing complaints related to on-market medical devices. Participate in complaint handling activities, such as complaint record review and closure and participate in escalated complaint investigation, as needed, as part of Illumina’s Quality Complaint Handling Unit.
This position is responsible for processing complaints which includes, documenting, evaluating and facilitating cross functional discussions with SMEs and ensuring that customer feedback is appropriately evaluated. Provide colleagues support as needed.
Responsibilities:
Conduct review of complaints for regulated products in a timely manner.
Identify, and triage potential adverse events and/or field actions and escalate to the QA Complaint leadership team in a timely manner
Participate in monitoring the QA Complaint Handling inbox and conduct tasks associated with rotational “monitor” activities
Ensure adequacy and accuracy of complaint records
Support Global complaints for case handling audits, when necessary
Complete other activities as assigned
All listed tasks and responsibilities are deemed essential functions to this position; however, business conditions may require reasonable accommodation for additional tasks and responsibilities.
Education:
Bachelor’s degree in an engineering or science discipline desired; advanced degree preferred
Quality Certification a plus (e.g., CQA, CQE)
Experience:
Minimum 2 years’ experience in complaint handling or direct experience working in medical device / in-vitro diagnostics (IVD) industry preferred
Knowledge and/or experience using Electronic Quality Management System for Complaint Handling is preferred
Good Documentation Practice (GDP) experience
Familiar with quality regulations and standards (21CFR820, ISO 13485, ISO 14971, and/or IVDR)
Skills:
Use of Microsoft Office Products and standard office tools
Ability to multi-task in a fast-paced environment and manage changing priorities with a high degree of self-motivation
Good written, oral, and interpersonal English communication skills
Willingness to work in shifts to support the US region (No night shift required)
Website: http://www.illumina.com/
Headquarter Location: San Diego, California, United States
Employee Count: 5001-10000
Year Founded: 1998
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Biotechnology ⋅ Genetics ⋅ Health Care ⋅ Medical
Visa Sponsorship: Sponsors work visas