Senior QC Reviewer / Planner 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, 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