Analytical Development Scientist – Pharma (cGMP)

NextPharma Technologies Holding Ltd; Livingston; On-site; GBP 50,000 - 75,000; Full time

Job summary

NextPharma Technologies Holding Ltd is seeking a Development Analyst to conduct analytical testing, stability studies, and method transfer from development through clinical manufacture. The role requires a pharmaceutical analysis background, experience in a cGMP, FDA and MHRA regulated environment, and the ability to work in a fast-paced, collaborative setting.

The successful candidate will mentor junior staff, contribute to data interpretation, and prepare high-quality client documentation and

Qualifications

• Qualified in Pharmaceutical Sciences, Chemistry, or related discipline and relevant industry background.
• Experience with analytical method development, validation and transfer to GMP standards.
• Proficient in analytical techniques including HPLC, Dissolution, GC and Karl Fischer.
• Experience with stability studies and data reporting to GMP/ICH standards.
• Ability to communicate clearly with colleagues and clients and deliver reports.

Responsibilities

• Actively participate in analytical activities to determine fitness for purpose and ensure regulatory compliance.
• Conduct analysis to support formulation development.
• Perform method development, validation and transfer of analytical methods for liquid filled products.
• Lead planning, execution and reporting of experimental work to high scientific standards.
• Provide expert technical support, troubleshooting, and root cause analysis to improve processes.

Skills

Analytical methods

HPLC

Dissolution

Gas Chromatography

Karl Fischer

Method development

Data interpretation

Education

HNC/HND/Science Degree or Equivalent in Pharmaceutical Sciences, Chemistry, or a related discipline

Tools

Chromeleon

Job description

NextPharma Technologies Holding Ltd is seeking a Development Analyst to conduct analytical testing, stability studies, and method transfer from development through clinical manufacture. The role requires a pharmaceutical analysis background, experience in a cGMP, FDA and MHRA regulated environment, and the ability to work in a fast-paced, collaborative setting.

The successful candidate will mentor junior staff, contribute to data interpretation, and prepare high-quality client documentation and