Quality Control Analyst

ZipRecruiter; Southwestern Ontario; On-site; CAD 60,000 - 80,000; Full time

Job summary

An innovative pharmaceutical firm in Essex is seeking a QC Analyst to contribute to the Pharmaceutical Development and Support department. The successful candidate will conduct Quality Control of products using advanced analytical techniques and ensure compliance with all standards. Ideal candidates will have a relevant degree, industry experience in analytical testing, and practical skills in HPLC and GC analysis. This is an excellent opportunity to join a forward-thinking team within the pharmaceutical sector.

Qualifications

• Relevant degree in a chemistry-based discipline.
• Proven industry experience in an analytical testing role, preferably in a GMP environment.
• A working knowledge and practical experience with HPLC and GC analysis, as well as Microsoft Office, particularly Word and Excel.

Responsibilities

• Conduct Quality Control of raw materials, bulk, and finished products using HPLC, GC, and wet chemical techniques.
• Analyse products to provide stability data for new product development and ongoing stability monitoring.
• Perform manual and automated tests and assays adhering to GMP standards.

Job description

Overview

ROLE OVERVIEW

An exciting role has arisen for a QC Analyst to join a leading Pharmaceutical company based in the Essex area. As the QC Analyst, you will be responsible for contributing to the Pharmaceutical Development and Support (PDS) department.

Responsibilities

• Conduct Quality Control of raw materials, bulk, and finished products using HPLC, GC, and wet chemical techniques in accordance with authorised test procedures.
• Analyse products to provide stability data for new product development and ongoing stability monitoring of commercial products, ensuring compliance with authorised test procedures.
• Perform manual and automated tests and assays with a high level of accuracy and precision, adhering to GMP standards, and operate associated analytical equipment.
• Collect, process, and report data using software packages such as Chromeleon, LIMS, Excel, and Word, and participate in the overall running of the laboratory, including equipment maintenance and calibration.

Role Requirements

• Relevant degree in a chemistry-based discipline.
• Proven industry experience in an analytical testing role, preferably in a GMP environment.
• A working knowledge and practical experience with HPLC and GC analysis, as well as Microsoft Office, particularly Word and Excel.

Key Words

Key Words: Laboratory Analyst / Quality Control / HPLC / GC / Wet Chemical Techniques / GMP / Pharmaceutical Development / Stability Data / LIMS / Analytical Testing

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.