Bioprocess Associate

Specialist, Upstream Manufacturing - 12 Month Contract - Shift

About the Company:

We are a global biopharmaceutical leader committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience, and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration, and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Our client operates a state-of-the-art Multi-Product Cell Culture (MPCC) biologics manufacturing facility in Dublin, Ireland—a major $1 billion investment. This facility significantly expands biologics manufacturing capacity and plays a central role in the company's global network.

Role Overview:

We are seeking to recruit a contingent Upstream Bioprocess Associate within the Manufacturing Operations group. Reporting to the Shift Lead, the Upstream Bioprocess Associate will support ongoing manufacturing operations within the facility, as well as commissioning and qualification activities for process equipment. This is a 24/7 shift role.

A typical day might include:

• Execution of commercial manufacturing processes according to established work instructions.
• Creation and updating of operating procedures and other relevant documentation for large-scale manufacturing.
• Operating production equipment within the assigned functional area.
• Adhering to Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs).
• Taking part in investigations and process optimization using scientific, engineering, and lean principles.
• Proficient use of process automation systems (e.g., Delta V, Syncade) and supporting business systems (e.g., SAP, OSI/Pi Historian, Maximo).
• Assisting with the review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representatives and providing input to related investigations and QA audit activities.
• Working with the manufacturing operations group, project design team, CQV team, and Automation/CSV teams to facilitate project design, validation, and operations.
• Engaging in and supporting a culture of continuous improvement and operational excellence through ownership of work processes, equipment, and a safe working environment.

Requirements:

• Minimum of Level 6 qualification in an Engineering/Science-related discipline; relevant experience in a similar regulated industry will also be considered (e.g., cGMP, ISO, or cleanroom industry experience strongly preferred).
• 3+ years’ working experience in a large-scale biopharmaceutical manufacturing facility.
• Hands-on experience with Delta V and MES or similar process control and data acquisition systems.
• Demonstrated ability to work independently and as part of a collaborative team.
• Strong problem-solving skills and the ability to adhere to scheduled timelines.
• Excellent communication skills and the ability to thrive in a cross-functional, fast-paced environment.
• Flexibility to work a 24/7 shift pattern due to the nature of manufacturing operations.

Core Behaviors:

• Passion: Pursuing excellence to help patients prevail, setting high standards, and treating colleagues and customers with respect and empathy.
• Innovation: Challenging the status quo, seeking bold ideas, encouraging constructive debate, and embracing change to drive innovative outcomes.
• Accountability: Owning outcomes, sharing information transparently, celebrating success, and fostering an inclusive environment.
• Speed: Acting with urgency and agility, prioritizing high-impact tasks, seeking efficient solutions, and making decisive actions.

Why Apply?

• Directly impact the lives of patients in their fight against serious diseases.
• Be part of an organization that encourages innovation, respects diversity, and invests in leadership development.
• Receive a highly competitive compensation package along with resources to support work-life balance and personal growth.