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.
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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
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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
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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