QC Chemistry Analyst: Method Validation & GMP

Wockhardt; Wrexham; On-site; GBP 26,000 - 38,000; Full time

Benefits offered by this job

Discounts on shopping

Salary sacrifice schemes

Sports and Social club

Subsidised canteen

Free parking

Job summary

Wockhardt in Wrexham is seeking a QC Analyst to design and execute analytical validation and verification for quality control. You will support the department by inspecting and analysing components, raw materials, products and processes to ensure compliance with quality standards.

The role requires strong GMP knowledge, experience with HPLC/UPLC/UV/GC methods, and the ability to take on some supervisory duties in a fast-paced pharmaceutical environment.

Qualifications

• Sound understanding of GMP, Health & Safety and COSHH regulations.
• Experience designing validation/verification protocols and writing validation reports.
• Ability to take on a limited supervisory role would be advantageous.
• Experience in pharmaceutical or equivalent laboratory environment with analytical validation.

Responsibilities

• Design and carry out HPLC/UPLC/UV/GC validation and/or verification.
• Support quality by inspection, sampling and analysis of components, raw materials, products and processes.
• Monitor quality through analytical testing and adherence to quality standards.

Skills

GMP knowledge

Health & Safety COSHH

Supervisory ability

Tools

HPLC

UPLC

UV

GC

Method Validation

Job description

Wockhardt in Wrexham is seeking a QC Analyst to design and execute analytical validation and verification for quality control. You will support the department by inspecting and analysing components, raw materials, products and processes to ensure compliance with quality standards.

The role requires strong GMP knowledge, experience with HPLC/UPLC/UV/GC methods, and the ability to take on some supervisory duties in a fast-paced pharmaceutical environment.