QC Analyst

QC Analyst – Pharmaceuticals

Location:
South London (Fully Site-Based)

Employment Type:
Full-Time

About the Role:

We are seeking a highly skilled and motivated
Quality Control Analyst
to join a pharmaceutical team in South London. This is a fully site-based role, ideal for someone with a strong background in analytical chemistry and a passion for maintaining high standards in a GMP-regulated environment.

Key Responsibilities:

• Perform routine and non-routine analysis of raw materials and finished pharmaceutical products using
  HPLC
  (essential),
  GC
  ,
  UV
  , and
  FTIR
  techniques (preferred).
• Demonstrate advanced troubleshooting skills with
  HPLC systems
  and lead
  Out of Specification (OOS)
  investigations.
• Ensure all testing is conducted in compliance with
  GMP
  standards and internal SOPs.
• Accurately document results and maintain laboratory records in accordance with regulatory requirements.
• Support method development and validation activities as needed.
• Collaborate with cross-functional teams to resolve quality issues and improve laboratory practices.

Requirements:

• Proven experience in a
  GMP-compliant pharmaceutical QC laboratory
  .
• Strong proficiency in
  HPLC
  is essential, including troubleshooting and OOS investigations.
• Experience with
  GC
  ,
  UV
  , and
  FTIR
  techniques is highly desirable.
• Excellent attention to detail and ability to work independently in a fast-paced environment.
• Strong communication and documentation skills.

What's on Offer:

• Competitive salary and benefits package.
• Opportunity to work in a dynamic and supportive team.
• Career development and training opportunities.

Key Words:

QC, quality control, analyst, analytical scientist, chemistry, chemist, chromatography, HPLC, GC, TLC, FTIR, UV Vis, techniques, GMP, Good Manufacturing Practice, laboratory technician, pharmaceutical, healthcare, supplement, medical.