Senior QC Analyst - GMP Lab, Validation & Training

Replimune

Abingdon

On-site

GBP 36,000 - 48,000

Full time

12 days ago
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Job summary

Replimune is seeking a QC Laboratory Technician at Milton Park to perform routine and non-routine QC testing in accordance with SOPs and established methods. This role involves reagent preparation, tissue culture support, equipment maintenance, and inventory management.

The position is on-site with a typical 5-day week, requiring meticulous attention to detail and strict adherence to cGMP/GDP practices, while supporting audits and documentation with a collaborative team.

Qualifications

  • 3 years or more of laboratory-based experience.
  • Competent analytical skills and attention for detail.
  • Understanding of GMP requirements.
  • Computer literacy (MS Word and Excel), good communication and organizational skills.
  • Ability to work independently and with others in a team.

Responsibilities

  • Perform QC testing of routine and non-routine samples according to SOPs.
  • Maintain cell lines by revival and passaging.
  • Manage QC sample and material receipts and inventory.
  • Routine equipment maintenance and troubleshooting.
  • Lead introduction of new equipment and participate in validation activities.
  • Write, review or update SOPs, protocols, and forms.
  • Support QC method transfers, validation and stability activities.
  • Adhere to cGMP and GDP practices.
  • General lab tasks including housekeeping and supplies inventory.
  • Assist investigations related to OOS/OOT results and deviations.

Skills

QC testing
Cell culture
GMP

Education

Degree in Chemistry/Biochemistry

Tools

MS Word
Excel

Job description

Replimune is seeking a QC Laboratory Technician at Milton Park to perform routine and non-routine QC testing in accordance with SOPs and established methods. This role involves reagent preparation, tissue culture support, equipment maintenance, and inventory management.

The position is on-site with a typical 5-day week, requiring meticulous attention to detail and strict adherence to cGMP/GDP practices, while supporting audits and documentation with a collaborative team.

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