Werfen · 4 hours ago
Technologist II, QC Lab
Werfen is a growing, family-owned company and a worldwide leader in specialized diagnostics. The QC Technologist II is responsible for executing a range of bench test procedures, maintaining documentation, and assisting with product performance investigations in the Quality Control laboratory.
Health CareHospitalManufacturingMedical Device
Responsibilities
Perform testing of biological raw materials and finished goods per relevant SOP
Perform testing for product validation and process validation on existing products
Perform testing and prepare reports as required for environmental monitoring or investigation of out-of-specification results, as required
Perform testing and assist with preparation of reports for various special projects as deemed necessary by technical review team
Responsible for tracking relevant trends
Maintain proper laboratory housekeeping and supply levels in the QC laboratory, including submission of purchase requisitions and inventory adjustments
Document all test results and maintain product release records (including electronic records)
Document existing product/process validation test results (including electronic records)
Maintain product testing database and perform relevant statistical analyses associated with product specifications as specified in laboratory SOPs
As required, assist with investigation and resolution of complaints, non-conforming material and product performance issues
Submit basic change orders to update procedures as required
Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures and processes
Other duties as assigned
Qualification
Required
High school diploma required; Bachelor's degree in Science or equivalent experience preferred
Thorough understanding of Good Laboratory Practices (GLP) required
Without Related degree: A minimum of two (2) years previous Quality Control lab (QC) and/or Quality Assurance (QA) experience required
With related degree, a minimum of one (1) years previous Quality Control lab (QC) and/or Quality Assurance (QA) experience required
Strong written and verbal communication skills
Ability to work independently and as part of a team
Proficiency with common laboratory techniques, such as pipetting and use of balances
Proficiency with Microsoft Office suite
Must occasionally lift up to 25 lbs
Preferred
Experience within a regulated medical device manufacturing or In-Vitro Diagnostic Device (IVDD) strongly preferred
Phlebotomy certification a plus
Proficiency with Large Enterprise Resources Planning (ERP) preferred
Company
Werfen
Werfen is a developer, manufacturer and distributer of IVD testing solutions.
H1B Sponsorship
Werfen has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (10)
2024 (12)
2023 (10)
2022 (2)
2021 (11)
2020 (8)
Funding
Current Stage
Late StageLeadership Team
Recent News
MarketScreener
2025-12-17
2025-12-08
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