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Production Technician

ProTech Recruitment Ltd
Posted 11 hours ago, valid for 15 days
Location

Trowbridge, Wiltshire BA14 7WJ

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

info
  • We are looking for a Reagent Production Technician to join a growing medical device company.
  • Candidates should have a BSc in a relevant scientific field and at least 2 years of hands-on experience in cGMP manufacturing, preferably in medical devices or pharmaceuticals.
  • The role involves manufacturing reagents, performing QC testing, and maintaining production records in a compliant facility.
  • A familiarity with ISO 13485 standards and experience with reagent formulation and process validation are essential.
  • The position offers a competitive salary, which will be discussed during the hiring process.

Reagent Production Technician

We are seeking a Reagent Production Technician to join a medical device company that is growing it's team. This is a great opportunity for someone who thrives in a fast-paced, collaborative setting and wants their work to directly support better health outcomes.

Responsibilities

  • Manufacture formulated reagents following SOPs in a cGMP / ISO 13485-compliant facility

  • Perform QC testing on raw materials, in-process, and finished reagents

  • Complete production records (MBRs, QC forms, validation documentation) with accuracy and care

  • Support validation activities (IQ/OQ/PQ), cleaning, equipment calibration, and general lab upkeep

  • Follow strict quality, safety, and regulatory procedures - and help maintain audit readiness

  • Keep training records up to date and contribute to continuous improvement efforts

Qualifications
  • BSc in a relevant scientific field (e.g., Chemistry, Biochemistry, Bio medical Science)

  • 2+ years' hands-on experience in cGMP manufacturing (medical devices or pharma preferred)

  • Familiarity with ISO 13485 standards and working in regulated environments

  • Experience with reagent formulation, QC, and process validation

  • Comfortable with electronic QMS platforms and Microsoft Office tools

  • Great attention to detail, excellent organisation, and a "get things done" mindset

  • Comfortable using Microsoft Office
  • A collaborative approach - you're someone who thrives in a close-knit, ambitious team

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.