GMP QC Specialist – Analytical Chemistry

NextPharma Technologies Holding Ltd; Livingston; Hybrid; GBP 28,000 - 38,000; Full time

Job summary

NextPharma Technologies Holding Ltd in Livingston, United Kingdom, seeks an analytical nuisance-solver to support the production of development and market finished products under GMP conditions across quality control and calibration.

You will be part of a team with Production and other analytical departments, performing sampling, QC testing, and method verification using HPLC, GC and dissolution while maintaining strict GMP and SOP adherence. Strong data reporting and communication are required.

Qualifications

• An understanding of drug development and manufacturing processes.
• Demonstrated technical competence in analytical activities to prescribed quality standards.
• Skilled in analytical techniques such as HPLC, Dissolution, GC and wet chemistry.
• Able to communicate well with others, both laboratory and non-laboratory based.

Responsibilities

• Work as part of a team alongside Production and other analytical departments including development and stability.
• Actively involved in performing analytical activities to determine fitness for purpose of starting materials, intermediate and finished products.
• Technically competent in analytical activities (e.g., pharmacopeial wet chemistry, HPLC, GC, Dissolution) for QC testing of raw materials, packaging components and finished products.
• Perform sampling of starting materials, packaging components and finished products.
• Perform cleaning verification analysis to assure suitability of Production equipment for subsequent use.
• Support calibration of key analytical equipment and measuring devices used in or on production equipment.
• Comply with company health and safety procedures.

Skills

Analytical thinking

Communication skills

Team player

Problem solving

Tools

HPLC

GC

Dissolution

Excel

Chromeleon software

Job description

NextPharma Technologies Holding Ltd in Livingston, United Kingdom, seeks an analytical nuisance-solver to support the production of development and market finished products under GMP conditions across quality control and calibration.

You will be part of a team with Production and other analytical departments, performing sampling, QC testing, and method verification using HPLC, GC and dissolution while maintaining strict GMP and SOP adherence. Strong data reporting and communication are required.