QC Analyst – Pharmaceuticals
Posted on Jun 16, 2026 by CV-Library
New Malden, Greater London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
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
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
Reference: 225252491
https://jobs.careeraddict.com/post/113415792
QC Analyst – Pharmaceuticals
Posted on Jun 16, 2026 by CV-Library
New Malden, Greater London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
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
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
Reference: 225252491
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