Senior QC Reviewer / Planner

Company: L M MANUFACTURING LIMITED
Apply for the Senior QC Reviewer / Planner
Location: Weedon Bec
Job Description:

Overview

Hit Apply below to send your application for consideration. Ensure that your CV is up to date, and that you have read the job specs first.

Weedon, Northamptonshire (NN7 4PP)

£34,000 – £36,000 per annum (depending on experience)

Permanent | Full Time | Monday to Friday

Benefits

  • 21 days annual leave plus UK bank holidays, with additional annual leave based on length of service (up to 4 extra days).
  • Statutory pension scheme, 7 days paid sick leave, Time Off in Lieu (TOIL) and free parking.
  • Stable long-term career opportunities and development support

Looking for a secure role in pharmaceutical quality?

Join LM Manufacturing as a Senior QC Reviewer / Planner supporting our Quality Control function.

This role is suited to candidates with experience in analytical data review, laboratory planning and compliance within pharmaceutical or regulated laboratory environments.

Key Responsibilities

  • Review analytical data generated from QC testing activities
  • Support planning and coordination of QC testing schedules
  • Review data from HPLC, UV, FTIR and Karl Fischer analysis
  • Support compliance with ALCOA++ principles, data integrity and GMP requirements
  • Assist with laboratory investigations including OOS, OOT and deviations
  • Review documentation in line with quality and regulatory standards
  • Support method validation and adherence to ICH and 21 CFR requirements
  • Work collaboratively across QC and wider site functions

What We’re Looking For

  • 5–8 years’ experience in Quality Control review or laboratory support
  • Experience reviewing analytical data in pharmaceutical or regulated laboratories
  • Familiarity with Chromeleon or similar laboratory software desirable
  • Understanding of data integrity, xlqdzyr GMP and compliance requirements
  • Strong attention to detail and documentation skills
  • Ability to support planning and prioritisation of QC activities

Desirable

  • Experience with OOS/OOT investigations
  • Exposure to method validation activities
  • Degree in Chemistry, Pharmacy or related scientific discipline

Why Join Us?

  • Competitive salary
  • Secure permanent employment
  • Supportive quality team
  • Opportunity to build your career in regulated pharmaceutical manufacturing

Apply now to join our Quality team

#J-18808-Ljbffr…

Posted: April 28th, 2026