QC Scientist

SRG; Manchester; On-site; GBP 28,000 - 44,000; Full time

Job summary

SRG is recruiting a QC Scientist for a busy CDMO in Greater Manchester. You will perform QC testing and support method development and validation activities to ensure product quality across early-stage development to approval.

The role involves hands-on UPLC/HPLC analysis, routine pharmacopeial testing, and contributing to transfers and CAPA processes within a GMP setting.

Qualifications

• Degree in Pharmaceutical Sciences, Chemistry, Biology, or a related field.
• Experience in a GMP pharmaceutical QC environment.
• Hands-on UPLC/HPLC experience; dissolution testing advantageous.

Responsibilities

• Hands-on analysis of products using UPLC/HPLC.
• Support method transfers, validations and development for assays, related substances/impurities, dissolution and cleaning validation methods.
• Investigate deviations and implement CAPAs.

Skills

UPLC/HPLC

GMP experience

Analytical testing

Education

Degree in Pharmaceutical Sciences, Chemistry, Biology or related field

Tools

UPLC/HPLC equipment

Job description

QC Scientist

Greater Manchester

SRG are recruiting for a QC Scientist to join a highly successful CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all the way through early-stage trials and to approval.

Due to continued growth and expansion of the business they are seeking to hire a QC Scientist to join their team in Greater Manchester to support the QC testing of products and assisting with Method Development & validation activities.

Key Responsibilities

• Hands-on analysis of products using UPLC/HPLC
• Conduct routine pharmacopeial testing, including:
  • IR identification
  • Appearance testing
  • pH testing
  • Content uniformity
  • Dissolution testing
  • Water content analysis
• supporting method transfers, validations and method development activities for assays, related substances/impurities, dissolution and cleaning validation methods.
• Supporting root cause investigations into deviations, non-conformance's and out-of-specification (OOS) results, and implementing appropriate CAPAs.

Qualifications & Experience

• Degree in a relevant scientific discipline such as Pharmaceutical Sciences, Chemistry, Biology, or a similar experience within a related field
• Prior experience in a Quality Control role within a GMP pharmaceutical environment.
• Hands on experience with UPLC / HPLC
• Prior experience working with Oral Solid Dose forms & Dissolution testing would be advantageous