8235
Lead Manufacturing Biotech Associate
County Meath, Ireland
Life Science
Fix Term Contract
8235
Posted on:
October 7, 2024
The Highlights:
- Working with world leading Pharmaceutical Company
- Work with leading edge technology
- Excellent professional development and leadership opportunities
The Role:
Elusav Recruitment have an exciting opportunity for a Lead Manufacturing Biotech Associate to join a leading global Pharma and Biopharma company in Dunboyne, County Meath, Ireland.
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.
Job Responsibilities:
- Carry out and support operations to achieve assigned duties.
- Deliver shift standard work for a team-based approach to batch progression.
- Complete COMMIT cards to highlight ways of working within our SDWT’s and Hubs and across our site that support our COMMIT culture.
- 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.
Job Requirements:
- 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 4 years’ experience in a GMP regulated environment.
- 4 years experience in a regulated GMP.
- 3 years experience in Biopharma industry, with direct experience of biologics manufacture would be desirable.
- Proven record of accomplishments in a regulated industry.
- Strong collaboration and cross-functional leadership skills to drive continuous improvement and promote knowledge sharing and implementation of Good Manufacturing Practices.
- Ability to effectively coach new trainees to build their skills so that they may become effective operations technicians and subject matter experts.
- Excellent trouble shooting and problem-solving skills to coach and mentor the teams through complex problems solving.
- On-the-floor current Good Manufacturing Practice (cGMP) manufacturing and familiarity with regulatory requirements.
- Proficiency with automated systems such as Manufacturing Execution System (MES - PAS X), Systems Applications and Products (SAP), Delta V etc.
- Knowledge of Lean.
- Familiar with all Safety, GMP, Environmental and Validation permits, policies and procedures.
- Familiar with plant equipment.
- Ability to read, write and understand technical information.
If you would like to learn more about the vacancy, apply now, or contact Thaissa Torres on Ttorres@elusav.com or +35315822807.
Apply Nowyou are applying for the role of
Lead Manufacturing Biotech Associate
Latest Vacancies
Browse all jobs
Subscribe to our newsletter!
Join our newsletter and receive leading industry insights and Job Opportunities, straight to your inbox.
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
