QC Analyst
Posted 3 days ago
- Liverpool, Merseyside
- Permanent
- Sponsored
- Expires In a month
Our client is a well-established, sterile GMP-accredited pharmaceutical manufacturer based in Liverpool, known for producing high-quality pharmaceutical products for both UK and international markets, exporting products to over 20 countries worldwide.
Are you a skilled QC Analyst with a passion for pharmaceutical quality and compliance? Do you thrive in a GMP-regulated environment and enjoy working with advanced analytical techniques? If so, we want to hear from you!
QC Analyst
Liverpool
As a QC Analyst, you will play a key role in ensuring the safety, efficacy, and compliance of pharmaceutical products through rigorous analytical testing.
The responsibilities of the QC Analyst include:
• Conduct routine and non-routine testing of raw materials and finished pharmaceutical products.
• Operate and maintain analytical instruments including HPLC, GC, ICP, wet chemistry and titrations.
• Assist in the introduction and validation of new methods and equipment
• Assist laboratory manager and technical managers in the capacity as a technical specialist providing advice and technical detail for routine analysis
• Perform equipment calibration and ensure accurate documentation.
• Assist in the investigation and documention of Out of Specification (OOS) and Out of Trend (OOT) results.
• Ensure strict adherence to cGMP and internal quality standards.
• Compile, interpret, and report analytical data for R&D and regulatory purposes.
The ideal candidate for the QC Analyst post will have:
• BSc (or higher) in Chemistry, Pharmaceutical Sciences, or a related discipline.
• 1–3 years of experience in a GMP-regulated pharmaceutical laboratory.
• Proficient in HPLC; experience with other analytical chemistry techniques is advantageous.
• Strong attention to detail and ability to work independently.
• Familiarity with regulatory guidelines (MHRA, FDA, ICH) is a plus.
In return, you’ll join a supportive team with opportunities for professional development, ongoing training, and career progression within a growing pharmaceutical business
Are you a skilled QC Analyst with a passion for pharmaceutical quality and compliance? Do you thrive in a GMP-regulated environment and enjoy working with advanced analytical techniques? If so, we want to hear from you!
QC Analyst
Liverpool
As a QC Analyst, you will play a key role in ensuring the safety, efficacy, and compliance of pharmaceutical products through rigorous analytical testing.
The responsibilities of the QC Analyst include:
• Conduct routine and non-routine testing of raw materials and finished pharmaceutical products.
• Operate and maintain analytical instruments including HPLC, GC, ICP, wet chemistry and titrations.
• Assist in the introduction and validation of new methods and equipment
• Assist laboratory manager and technical managers in the capacity as a technical specialist providing advice and technical detail for routine analysis
• Perform equipment calibration and ensure accurate documentation.
• Assist in the investigation and documention of Out of Specification (OOS) and Out of Trend (OOT) results.
• Ensure strict adherence to cGMP and internal quality standards.
• Compile, interpret, and report analytical data for R&D and regulatory purposes.
The ideal candidate for the QC Analyst post will have:
• BSc (or higher) in Chemistry, Pharmaceutical Sciences, or a related discipline.
• 1–3 years of experience in a GMP-regulated pharmaceutical laboratory.
• Proficient in HPLC; experience with other analytical chemistry techniques is advantageous.
• Strong attention to detail and ability to work independently.
• Familiarity with regulatory guidelines (MHRA, FDA, ICH) is a plus.
In return, you’ll join a supportive team with opportunities for professional development, ongoing training, and career progression within a growing pharmaceutical business