Reagent Production Technician

JR United Kingdom; Cardiff; On-site; GBP 30,000 - 50,000; Full time

Job summary

An innovative healthcare technology company is seeking a dedicated individual to join their team in Cardiff. This role focuses on adhering to strict manufacturing procedures in a cGMP compliant environment, ensuring high-quality production of diagnostic reagents. The ideal candidate will have a background in scientific disciplines, experience in cGMP manufacturing, and a proactive approach to problem-solving. Join a forward-thinking organization committed to expanding access to care and making a difference in the healthcare landscape. If you are detail-oriented and thrive in a collaborative environment, this opportunity is perfect for you.

Qualifications

• BSc in a relevant scientific discipline required.
• 2+ years experience in cGMP manufacturing of formulated reagents.

Responsibilities

• Follow SOPs for production of formulated reagents.
• Maintain accurate production records and engage in quality management.

Skills

Attention to Detail

Teamwork

Microsoft Office

cGMP Compliance

Problem Solving

Education

BSc in a relevant scientific discipline

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Teams

Job description

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Client:

binx health

Location:

trowbridge, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

8

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

Who We Are:

binx health is a healthcare technology and diagnostics company focused on expanding access to care. The binx io is the world’s first FDA-cleared, CLIA-Waived, point-of-care platform for chlamydia and gonorrhoea testing in both males and females. Our rapid, molecular platform brings rapid, accurate and convenient infectious disease testing to clinical settings nationwide. Our solutions have the ability to broaden access to care for millions and put proprietary testing solutions in the hands of clinicians everywhere. We work with universities, hospitals, clinics, public health departments, k-12 schools, employers and other organizations to provide patient-centric solutions for their communities. Our Values:

Our Values:

We are…

Bold – Tenacious – One Team – Fixated on Our Mission

At binx health, we know a diverse workforce adds to our collective value and strength as an organization. People of colour, the LGBTQIA+ community, disabled candidates and veterans are strongly encouraged to apply. binx health is proud to be an Equal Opportunity Employer, committed to equal employment opportunity and fair, equitable compensation regardless of race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

The Position:

Responsibilities:

• Follow manufacturing procedures (SOPs) for the production of formulated reagents at a cGMP/ISO13485 compliant binx production site
• 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
• Follow and engage in the Quality Management System
• Perform an active role in identifying improvements to the manufacture processes, including the updates of Standard Operating Procedures and Job Aids
• Assisting with experimentation to define and characterise improvements for manufacture
• Ad-hoc tasks may be assigned due to business needs.

Education, Experience and Demonstrated Skills:

• BSc in a relevant scientific discipline
• Ability to strictly adhere to production procedures
• Practical experience handling reagents
• High attention to detail
• Organised and logical approach to tasks
• Demonstrated ability to work as part of a team
• Competent in the use of Microsoft Office (Word Excel, PowerPoint, Teams)
• Proactive and efficient attitude
• Ability to adapt to new tasks
• Experience (2y+) in cGMP manufacturing of formulated reagents (pharma/ medical devices industry)
• Equipment and process validation
• Completion and maintenance of production records to procedures
• Background in formulations manufacturing
• Knowledge of LEAN manufacturing
• Experienced in ISO13485 / cGMP compliance