C&Q Engineer Opportunity
Our client in Dublin is a Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines.
This contract opportunity involves working as a Filling C&Q Engineer on a project focused on filling line systems, including Syringe and Vial line/isolators, Lyos, and associated equipment for a Sterile Drug product facility.
* Documentation development and execution of CQV testing for filling line systems
* Meet key project deliverables for safety, CQV schedule, and quality of project-related documentation/electronic records
The ideal candidate should hold a Bachelor's degree in a scientific, technical, or engineering discipline with 3-5 years of experience within the pharmaceutical industry and familiarity with Sterile Drug Product filling line experience. A strong foundation in regulatory compliance, risk management, and quality assurance principles will be essential in this role.
We are seeking a highly skilled and experienced Filling C&Q Engineer to join our team. The successful candidate will have excellent analytical skills, a strong attention to detail, and the ability to work effectively in a fast-paced environment.
In addition to your technical expertise, you will possess excellent communication and interpersonal skills, enabling effective collaboration with cross-functional teams, including production staff, quality assurance personnel, and senior management.
A thorough understanding of Good Manufacturing Practice (GMP) regulations, current GMP guidelines, and industry standards will be necessary to ensure that all aspects of the filling process meet regulatory requirements.
Your professional approach, combined with your passion for innovation, will make you a valuable asset to our organization.