Job Overview
We are seeking a skilled professional to join our team in Ireland, focusing on validation engineering and quality control.
Key Responsibilities:
* Support and assist with Quality Control compliance for equipment qualification activities, ensuring adherence to safety and regulatory standards.
* Help document and execute equipment qualification processes, from initial assessments to Operational Qualification (OQ), emphasizing accuracy and attention to detail.
* Follow established procedures and protocols for new equipment qualification to promote quality practices within workflows.
* Assist with the review and completion of Test Outlines and Procedures (TOPs), verifying alignment with quality specifications.
* Support the planning and organization of commissioning materials and consumables, ensuring they meet required quality standards.
Our ideal candidate will possess at least 2 years of relevant experience in Validation Engineering or Quality Control. They will work alongside senior team members, assisting in maintaining quality standards and ensuring compliance throughout all equipment qualification activities.
The successful candidate will be responsible for supporting and assisting with Quality Control compliance, documenting and executing equipment qualification processes, following established procedures, and assisting with the review and completion of Test Outlines and Procedures.
We offer a competitive compensation package, including pension fund, medical aid, dental care, income protection, and group life assurance. Our company values integrity, serving each other, serving society, and working for our future.
Requirements
* BS or MS in a relevant science or engineering field, or equivalent experience.
* 2+ years of industry-related experience in a similar role.
* Strong oral and written communication skills, with a focus on clear documentation and reporting.
* Strong problem-solving skills with a focus on Quality Control.
* Customer-service oriented and able to collaborate well with internal teams and external vendors.
* Familiarity with life science manufacturing processes such as biotech, aseptic fill/finish, oral solid dose (OSD), and gene therapy, or equivalent experience.