Instrument Lifecycle Coordinator

SRG; Loughborough; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading CDMO is seeking an Instrument Lifecycle Coordinator in Loughborough for a 12-month contract. This role involves coordinating qualification activities for laboratory instruments, maintaining compliance, and supporting calibration schedules. Ideal candidates should have at least 2 years in a GxP environment and familiarity with analytical instruments like HPLC. Strong organizational skills and a degree in analytical sciences are essential.

Qualifications

• At least 2 years' experience in a GxP-regulated pharmaceutical environment.
• Recent hands-on involvement in equipment qualification and calibration processes (IQ, PQ, OQ, DQ).
• Familiarity with analytical instruments such as HPLC and GC.

Responsibilities

• Coordinating qualification activities for laboratory instruments.
• Assisting with procurement, delivery, and installation of new equipment.
• Supporting calibration and maintenance schedules.

Skills

Experience in GxP-regulated environment

Hands-on in equipment qualification

Familiarity with HPLC and GC

Experience with Chromatography Data Systems

Strong organizational skills

Attention to detail

Excellent communication abilities

Education

Degree in analytical sciences or related discipline

Tools

Chromatography Data Systems (e.g., Empower)

Electronic Laboratory Notebooks (ELN)

Job description

Exciting Opportunity: Instrument Lifecycle Coordinator

A leading CDMO is seeking an Instrument Lifecycle Coordinator to join their Laboratory Services team in Loughborough on a 12-month contract.

Job Title: Instrument Lifecycle Coordinator
Vacancy Type: 12-Month Contract (with potential extension)
Location: Loughborough
Salary: £14.49 per hour
Hours: 37.5 per week

About the Role

In this role, you'll be central to ensuring laboratory instruments are qualified, maintained, and compliant throughout their lifecycle. You'll work closely with internal teams and external vendors to keep projects on track and equipment operating to the highest standards.

Key Responsibilities

• Coordinating qualification activities for laboratory instruments, from planning through execution and documentation
• Assisting with procurement, delivery, and installation of new equipment to meet project timelines
• Supporting calibration and maintenance schedules to ensure reliability and compliance
• Preparing and reviewing qualification protocols, reports, and related documentation in line with GxP requirements
• Acting as a point of contact for internal stakeholders and external service providers

What We're Looking For

• At least 2 years' experience in a GxP-regulated pharmaceutical environment
• Recent hands-on involvement in equipment qualification and calibration processes (IQ, PQ, OQ, DQ)
• Familiarity with analytical instruments such as HPLC and GC
• Experience using Chromatography Data Systems (e.g., Empower) and Electronic Laboratory Notebooks (ELN)
• A degree in analytical sciences or a related discipline
• Strong organizational skills, attention to detail, and excellent communication abilities

This is a fantastic opportunity to gain exposure to a dynamic CDMO environment and contribute to critical laboratory operations. Apply today and take the next step in your career!

For more information, please contact Selby De Klerk at SRG