We are seeking a talented professional to join our team at an award-winning Pharmaceutical organization based in Cork.
This is an excellent opportunity for individuals who want to work with a leading multinational company that excels in its field.
Key Responsibilities:
* Evaluate and maintain the highest standards of Quality, Compliance, and Safety across various activities.
* Collaborate with a team to enhance performance within the Technology Transfer group and Tech Ops.
* Lead equipment qualification projects, provide technical support, and develop protocols to support equipment validation.
* Review and own Global Change management records, assessing their impact as required.
* Recommend technical approaches aligned with global and local standards.
* Stay up-to-date with new technologies in vaccine and biopharmaceutical processing and implement process improvements through innovation.
* Contribute to driving a culture of Continuous Improvement by deploying MPS within Tech Ops on projects such as problem-solving and cycle time reduction.
* Maintain stakeholder relationships with decision-makers, corporate colleagues, and cross-functional teams.
* Participate in and comply with our Manufacturing Division Quality Management System (QMS) requirements.
* Lead Knowledge Management efforts within the team.
Requirements:
* Experience in process engineering within the biopharmaceutical/vaccine environment would be beneficial.
* Degree or Master's in a Science or Engineering discipline (preferably Biotechnology).
* Prior experience with equipment commissioning, qualification, and validation.
The estimated salary for this position is $120,000 - $180,000 per annum, depending on qualifications and experience.