Lead Biotech Associate

PE Global is currently recruiting for a Lead Biotech Associate for a leading multi-national Biotech client based in Meath.

This is an initial 11-month contract shift position in a new state of the art single use multi-product biotech facility. The Lead Manufacturing Biotech Associate is a leader with strong interpersonal, communication, and collaboration skills. The Lead Manufacturing Biotech Associate is responsible for supporting the manufacturing process, while creating an inclusive culture that energizes a Safety First, Quality Always, with a continuous improvement mindset in a new state of the art single use multi-product biotech facility.

ROLE:

• Carry out and support operations to achieve assigned duties.
• Deliver shift standard work for a team-based approach to batch progression.
• Conduct sampling/ in-process testing supporting the manufacturing and validation processes.
• Document executed activities necessary to allow proper accountability and traceability of production records, Right First Time (RFT).
• Author, review, and/or edit procedures and technical documents to ensure the documents are in accordance with cGMP requirements.
• Provide coaching to the shift teams on the RFT approach to documentation.
• Ensure that all assigned tasks related to manufacturing documentation support is in accordance with good manufacturing practices.
• Initiate/ maintain housekeeping in all work areas.
• Identify, escalate and address compliance, environmental, safety, and process deviations as appropriate.
• Support execution of safety walkdowns, audits/ inspections, risk assessment, implementation of agreed upon actions, etc.
• Ensure incident investigations are fully supported with improvement actions implemented and participate in investigations arising from manufacturing documentation aspects as and when required.
• Coach and provide oversight on the shop floor to identify potential issues before they arise.
• Actively participate on cross-functional manufacturing teams to advance projects, goals and deliverables.
• Lead approved projects and continuous improvement initiatives that are in alignment with the site strategies.
• Lead straight-through document accuracy metrics and the development of a CI framework.
• Support site functional initiatives to improve compliance status and operational efficiency of the site.
• Run handover boards and provide key updates to shift leads for handover.
• Be escalation point of contact (POC) for troubleshooting, supporting task execution, problem solving,
• CI projects and assist with the resolution of issues/ delays.
• Take ownership of activities within a suite and act as a delegate for the shift lead if they are unavailable.
• Ensure process equipment is maintained including preventative maintenance, equipment troubleshooting and repairs to ensure continuous, reliable and repeatable operation of equipment.
• Effectively manage and schedule equipment shutdowns.
• Ensure resources are available, thereby minimizing downtime.

REQUIREMENTS:

• Minimum of a Bachelors Level 8 degree in Science, Engineering or other Technical Discipline or a Level 7 qualification in a science or engineering discipline with a minimum of 5 years’ industry experience .
• 5 years experience in a GMP environment.
• 3 years experience in Biopharma industry, with direct experience of biologics manufacture.
• Proven record of accomplishments in a regulated industry required

Interested candidates should submit an updated CV.

Please click the link below to apply, call Seán on +353 21 4297900 or alternatively send an up to date CV to sean.molloy@peglobal.net 

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***