Job Overview
As a Quality Assurance Validation Specialist, you will be responsible for supporting new validation and commissioning initiatives across the site. This involves periodically reviewing validated systems within drug substance, facilities, and laboratories to ensure ongoing compliance with cGLP and cGMP.
Key responsibilities include streamlining processes and adhering to business objectives in the validation department, laboratories, and projects. Additionally, you will drive QA compliance to achieve best-in-class standards across the industry, serving as a benchmark for others.
Collaboration is key, as you will work closely with project-based teams, including Validation, Microbiology, IT, Engineering utilities, and other departments to provide QA support for commissioning, decommissioning, and validation projects across the site.
Required Skills and Qualifications
To succeed in this role, you should possess excellent communication and problem-solving skills. Strong attention to detail and organizational abilities are also essential, as well as the ability to prioritize tasks effectively.
* Support the day-to-day running of the validation department, laboratories, and projects.
* Drive QA compliance to achieve best-in-class standards across the industry.
* Collaborate with project-based teams to provide QA support for commissioning, decommissioning, and validation projects.
Benefits
This role offers a unique opportunity to contribute to the success of the organization while developing your skills and expertise. If you are a motivated and results-driven individual looking to make a meaningful impact, we encourage you to apply.