CQV Engineer Position
We are recruiting a CQV Engineer for a long-term opportunity.
Key Responsibilities:
* Prepare, execute and report on CQV activities for assigned systems to include planning, generation of user requirements, facilitation of design qualification, testing and validation, and documentation review.
* Review and approve project documentation to ensure technical accuracy and adherence to regulatory standards.
* Support system risk assessments with multiple stakeholders.
Essential Qualifications:
* A degree in an Engineering or Science discipline.
* At least 5 years experience in the biotechnology and/or pharmaceutical industry, in a CQV role.
* Proven experience in authoring, reviewing and executing CQV activities on various equipment and systems.
Benefits of Working with Us:
As a CQV Engineer, you will have opportunities to work with diverse stakeholders, develop your skills and expertise, and contribute to the success of our organization.
In this role, you will be responsible for ensuring that our facilities, systems and equipment meet regulatory requirements and industry standards.
About the Role:
This is a challenging and rewarding position that requires strong technical skills, excellent communication and collaboration skills, and a commitment to quality and safety.