Senior QC Reviewer & Laboratory Planner

Senior QC Reviewer & Laboratory Planner
Senior QC Reviewer | QC Compliance Reviewer | Laboratory Planner
LM Manufacturing Limited – Northamptonshire (NN7, Weedon Bec)
Permanent | Full Time | Monday to Friday

LM Manufacturing Limited is seeking an experienced Senior QC Reviewer & Laboratory Planner to join our growing Quality Control team within a pharmaceutical manufacturing environment.

This Senior QC Reviewer & Laboratory Planner role is ideal for candidates with strong experience in analytical data review, laboratory coordination, GMP compliance, QC documentation review, and QC planning activities within regulated pharmaceutical laboratories.

The successful Senior QC Reviewer will support laboratory review activities, QC compliance, laboratory planning, GMP documentation review, and coordination of Quality Control testing schedules.

Key Responsibilities:

• Review analytical data generated from QC testing activities
• Coordinate and support QC laboratory testing schedules and planning activities
• Review analytical data from HPLC, UV, FTIR, and Karl Fischer testing
• Ensure compliance with ALCOA++, data integrity, and GMP requirements
• Support laboratory investigations including OOS, OOT, deviations, and CAPAs
• Review laboratory documentation in line with quality and regulatory standards
• Support method validation and verification activities
• Ensure compliance with ICH guidelines and 21 CFR requirements
• Work collaboratively with QC, QA, Production, and other site departments
• Support continuous improvement initiatives within the QC function

What We’re Looking For:

• 5–8 years’ experience within Quality Control in a pharmaceutical or regulated laboratory environment
• Strong experience as a QC Reviewer, GMP Reviewer, or QC Compliance Reviewer
• Experience reviewing analytical data and laboratory documentation
• Hands-on knowledge of HPLC, UV, FTIR, and Karl Fischer analysis
• Good understanding of GMP, data integrity, and regulatory compliance
• Experience with Chromeleon or similar CDS software preferred
• Strong organisational skills and attention to detail
• Excellent communication and problem-solving skills

Desirable:

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

Benefits:

• Competitive salary depending on experience
• 21 days annual leave plus bank holidays
• Additional annual leave based on service
• Pension scheme
• Paid sick leave after probation
• Time Off in Lieu (TOIL)
• Free parking
• GP on-demand service
• Stable long-term career opportunities and development support

Location: NN7, Weedon Bec, Northamptonshire
Job Type: Permanent | Full Time | Day Shift

Please note: Sponsorship is not available for this role.