QC Scientist

ZipRecruiter; England; On-site; GBP 30,000 - 50,000; Full time

Job summary

An innovative global pharmaceutical company is seeking a skilled analyst to join their team for a 6-month contract in West Sussex. The role involves testing production samples and performing qualitative and quantitative analyses using advanced techniques like HPLC and Karl Fischer titration. You will ensure compliance with GMP regulations and support OOS investigations, contributing to the quality assurance of pharmaceutical products. This is an excellent opportunity for those passionate about science and quality in the pharmaceutical industry, offering a chance to make a tangible impact in a dynamic environment.

Qualifications

• Degree in Chemistry or related field with experience in GMP-regulated labs.
• Proficient in HPLC and Karl Fischer techniques.

Responsibilities

• Test production and stability samples to meet lead-time targets.
• Perform qualitative and quantitative analysis of antibiotic powders.

Skills

Analytical Techniques

HPLC

Karl Fischer Titration

Quality Systems (GLP, GMP)

OOS Investigations

Education

Degree in Chemistry

Degree in Pharmaceutical Sciences

Degree in a related scientific field

Tools

Electronic Lab Systems

LIMS

Job description

Job Description

CY Partners have a new position available with our client who is a Global Pharmaceutical Company, with a site based in West Sussex. You will be joining on an initial 6 month contract.

Key Responsibilities:

• Test routine production and stability samples in line with lead-time targets.
• Perform qualitative and quantitative analysis of antibiotic powders and solid dose forms using techniques such as HPLC, Karl Fischer, and dissolution testing.
• Calibrate and maintain laboratory equipment in accordance with SOPs.
• Conduct and support Out of Specification (OOS) investigations, liaising with relevant departments as needed.
• Review and verify analytical data produced by other analysts.
• Carry out validation of analytical methods and equipment as required.

Key Requirements:

• Degree in Chemistry, Pharmaceutical Sciences or a related scientific field.
• Experience working in a GMP-regulated pharmaceutical laboratory.
• Proficient in analytical techniques including HPLC and Karl Fischer titration.
• Strong understanding of GLP, GMP and quality systems.
• Experience in conducting and documenting OOS investigations.
• Familiarity with electronic lab systems and LIMS is advantageous.