About the Role

As a QC Analyst, you will be responsible for both routine and project-based analytical activities related to cleaning verification and validation. You will play a key role in ensuring product quality and compliance, working closely with cross-functional teams within Quality, Manufacturing, and Validation.

Key Responsibilities

• Perform cleaning verification and cleaning validation in accordance with approved methods and protocols

• Execute analytical testing using HPLC and GC techniques

• Document and review results in compliance with GMP standards and data integrity requirements

• Investigate and troubleshoot analytical results and laboratory methods when necessary

• Ensure adherence to internal SOPs and regulatory requirements

• Contribute to continuous improvement of laboratory processes and documentation practices

• Collaborate cross-functionally with relevant stakeholders

Requirements (Must Have)

• Proven experience working as a QC Analyst in a GMP-regulated environment

• Hands-on experience with cleaning verification and/or cleaning validation

• Strong practical experience with HPLC and GC

• Solid understanding of GMP, documentation practices, and data integrity principles

• Ability to work independently, in a structured and detail-oriented manner

• Fluent in English, both written and spoken

Preferred Qualifications

• Experience within pharmaceuticals, consumer health, or life sciences

• Previous experience working as a consultant

• Experience with method validation, method transfer, or troubleshooting

• Experience collaborating closely with Validation or Manufacturing teams

• Familiarity with LIMS or similar laboratory systems