Analytical Scientist

Vertage Inc.; Moreton; On-site; GBP 42,000 - 62,000; Full time

Job summary

Vertage Inc. is seeking an experienced Analytical Scientist to perform testing of pharmaceutical products in a GMP-regulated laboratory. You will use techniques such as HPLC, Dissolution Testing and Karl Fischer Titration to ensure products meet quality and regulatory standards.

You will lead analytical testing, review data, and support method validation while ensuring compliance with ALCOA+ and GMP. This role involves collaboration across functions and participation in continuous improvement

Qualifications

• Degree in Chemistry, Analytical Chemistry, Biochemistry, or related science.
• Minimum 3 years' GMP pharmaceutical laboratory experience.
• Strong hands-on experience with HPLC, Dissolution Testing, and Karl Fischer Analysis.
• Experience testing oral solid dose products (tablets/capsules).
• Strong problem-solving, communication, and compliance skills.

Responsibilities

• Perform analytical testing of drug substances and finished products.
• Operate HPLC, Dissolution, and Karl Fischer equipment.
• Review and approve analytical results and laboratory documentation.
• Investigate laboratory issues and support method validation activities.
• Ensure compliance with GMP, ALCOA+, and quality standards.
• Support audits, continuous improvement, and cross-functional collaboration.

Skills

Problem solving

Communication

Compliance

Education

Degree in Chemistry or related science

Tools

HPLC

Dissolution Testing

Karl Fischer Titration

Job description

Analytical Scientist / Analytical Chemist (GMP Laboratory)

We are looking for an experienced Analytical Scientist to perform testing of pharmaceutical products in a GMP-regulated laboratory. The role involves using analytical techniques such as HPLC, Dissolution Testing, and Karl Fischer Titration to ensure products meet quality and regulatory standards.

Key Responsibilities

• Perform analytical testing of drug substances and finished products.
• Operate HPLC, Dissolution, and Karl Fischer equipment.
• Review and approve analytical results and laboratory documentation.
• Investigate laboratory issues and support method validation activities.
• Ensure compliance with GMP, ALCOA+, and quality standards.
• Support audits, continuous improvement, and cross-functional collaboration.

Requirements

• Degree in Chemistry, Analytical Chemistry, Biochemistry, or related science.
• Minimum 3 years' GMP pharmaceutical laboratory experience.
• Strong hands-on experience with HPLC, Dissolution Testing, and Karl Fischer Analysis.
• Experience testing oral solid dose products (tablets/capsules).
• Strong problem-solving, communication, and compliance skills.