QC Scientist - GMP Pharma, HPLC & Method Development

SRG; Greater Manchester; On-site; GBP 32,000 - 42,000; Full time

Job summary

SRG is recruiting a QC Scientist to join a leading CDMO in Greater Manchester. The role focuses on QC testing of products and supporting method development and validation activities across the product lifecycle.

This is a hands-on, on-site role at a rapidly expanding site. You will perform UPLC/HPLC analyses, routine pharmacopeial testing, dissolution, content uniformity and contribute to investigations and CAPAs in a GMP environment.

Qualifications

• Degree in Pharmaceutical Sciences, Chemistry, Biology, or related field.
• Experience in a GMP pharmaceutical QC role.
• Hands-on UPLC/HPLC experience.
• Experience with Oral Solid Dose and dissolution would be advantageous.

Responsibilities

• Hands-on analysis of products using UPLC/HPLC.
• Routine pharmacopeial testing: IR identification, appearance testing, pH, content uniformity.
• Dissolution testing and water content analysis.
• Supporting method transfers, validations and development for assays/impurities/dissolution/ cleaning validation methods.
• Investigating deviations and OOS and implementing CAPAs.

Skills

UPLC/HPLC

Quality Control

GMP compliance

CAPA investigations

Education

BSc/MSc in Pharmaceutical Sciences, Chemistry, or Biology

Tools

UPLC/HPLC instrumentation

Dissolution testing equipment

Job description

SRG is recruiting a QC Scientist to join a leading CDMO in Greater Manchester. The role focuses on QC testing of products and supporting method development and validation activities across the product lifecycle.

This is a hands-on, on-site role at a rapidly expanding site. You will perform UPLC/HPLC analyses, routine pharmacopeial testing, dissolution, content uniformity and contribute to investigations and CAPAs in a GMP environment.