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Posted on March 31, 2022 in UK Jobs

UK Reagent Production Technician

Who we are

binx health has the world’s fastest FDA-cleared molecular platform for CT/NG testing for male and female samples. We also have a broad suite of offerings in sample collection for large corporate partners for broadened access to STI and COVID-19 care. Our molecular point of care platform brings rapid, accurate, and convenient infectious disease testing to people where they live, work, and shop. Our solutions offer front-end engagement, and end-to-end logistics in concert with our reference lab partners to offer partners “turn-key” answers for their infectious disease testing needs. Our solutions broaden access to care for millions and put proprietary testing solutions in the hands of clinicians everywhere, including in the ever-expanding footprint of retail health. Our suite of medical guideline-driven sample collection and laboratory testing solutions for STIs and COVID-19 are designed to reach the many who are unwilling or unable to visit a physical location.

The Position

We are looking for a Production Technician to work the day-to-day duties of our reagents department.

Responsibilities

  • Follow manufacturing procedures (SOPs) for the production of formulated reagents at a cGMP/ISO13485 compliant binx production site
  • Follow QC procedures for the testing of incoming raw materials, goods in, formulated reagents, and final product
  • Operate according to cGMP and ISO13485
  • Produce and maintain accurate production records (MBRs and forms) for manufacturing, QC, and IQ/OQ/PQ activities
  • Implement site management activities (equipment maintenance and calibration, cleaning, health and safety, waste management, etc) as instructed by the production manager
  • Maintain training records up to date

Education, Experience, and Demonstrated Skills

  • BSc in a relevant scientific discipline
  • Experience (2y+) in cGMP manufacturing of formulated reagents (pharma/ medical devices industry)
  • Commercial in vitro diagnostic/medical devices product manufacturing experience
  • Experienced in ISO13485 / cGMP compliance
  • Verification & Validation experience
  • QC and validation for raw materials, reagents, and finished product
  • Ability to strictly adhere to production procedures
  • Completion and maintenance of production records to procedures
  • Background in formulations manufacturing
  • ISO13485 / cGMP compliance
  • Equipment and process validation
  • Experience working with eQMS systems
  • Attention to detail & well organized
  • Competent in the use of Microsoft Office (Word Excel, PowerPoint, Teams)

binx health, Inc. is an Equal Opportunity Employer For interested applicants, please submit resumes to careers@mybinxhealth.com