Senior Analytical Scientist: Global Method Transfer & Lifecycle

VRS Recruitment

Macclesfield

Hybrid

GBP 55,000 - 75,000

Full time

13 days ago
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Benefits offered by this job

Flexible hybrid working model
Collaborative environment

Job summary

VRS Recruitment is seeking an experienced Analytical Scientist to support commercial drug products at a world-class pharmaceutical facility in Macclesfield. You will ensure analytical performance, robustness, and regulatory compliance across an OSD portfolio, with potential international travel.

The role demands a degree (MSc/PhD) in a scientific field and strong experience in drug product analytics, cGMP, and cross-functional teamwork within a global pharma setting.

Qualifications

  • Degree, MSc or PhD in a scientific field.
  • Strong industry experience in drug product analytical development and understanding of OSD lifecycles.
  • Working knowledge of SHE principles and cGMP compliance.

Responsibilities

  • Serve as the key point of contact for analytical testing of commercial drug products.
  • Support global manufacturing sites and CMOs with analytical expertise.
  • Collaborate across Manufacturing, QA, QC, Regulatory Affairs and External Sourcing.
  • Oversee method transfers, change control assessments, and market access projects.
  • Provide technical leadership on complex analytical investigations and lifecycle management.
  • Potential involvement in hands-on lab work and international travel.

Skills

Analytical development
Cross-functional collaboration
cGMP compliance
Communication
Lean methodologies

Education

Degree/MSc/PhD in scientific field

Tools

HPLC
GC

Job description

VRS Recruitment is seeking an experienced Analytical Scientist to support commercial drug products at a world-class pharmaceutical facility in Macclesfield. You will ensure analytical performance, robustness, and regulatory compliance across an OSD portfolio, with potential international travel.

The role demands a degree (MSc/PhD) in a scientific field and strong experience in drug product analytics, cGMP, and cross-functional teamwork within a global pharma setting.

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