Manufacturing Engineer

Are you a skilled professional passionate about enhancing manufacturing processes within the biopharmaceutical industry? We're recruiting a Manufacturing Engineer to join a dynamic team dedicated to operational excellence, continuous improvement, and quality assurance.

Key Responsibilities:
As a Manufacturing Engineer, you will:

• Collaborate with the Downstream Integrated Process Team (IPT) to ensure on-time delivery of production schedules while adhering to safety and quality standards.
• Manage and oversee material handling processes to maintain quality and delivery metrics.
• Lead and own quality investigations, performing root cause analysis and implementing corrective actions.
• Monitor production quality metrics, ensuring timely documentation, line clearance, and adherence to SOPs.
• Drive and support continuous improvement projects focusing on schedule optimization, equipment efficiency, and delivery capabilities.
• Act as a liaison between shift operations and day teams, standardizing processes across IPT teams.
• Promote and sustain a culture of audit readiness, supporting both internal and external audits.
• Facilitate Root Cause Analysis (RCA) sessions for safety and quality events, ensuring actions are effectively resolved.
• Lead and support area change controls, CAPAs, and quality initiatives, including documentation updates.
• Provide coaching and support to team members, sharing best practices to enhance operational excellence.
• Partner with cross-functional teams to troubleshoot and resolve manufacturing challenges with innovative solutions.

Skills & Qualifications:
The ideal candidate will have:

• A Level 7 degree in Science, Engineering, or a related field (or equivalent relevant experience).
• Experience in a GMP environment with a focus on change management and technical writing for quality investigations.
• Strong organizational skills, self-motivation, and the ability to work effectively both independently and collaboratively.
• Excellent communication skills, with proficiency in Microsoft Office tools.
• High attention to detail and experience working with GMP Documentation Management Systems.
• Previous experience across functions such as Quality, Engineering, or Supply Chain (preferred but not required).

Why This Opportunity?
This is a fantastic chance to work with a forward-thinking team in a challenging and rewarding environment. You'll play a pivotal role in ensuring operational success and making a tangible impact in downstream manufacturing.

The Next Step for You

Should this position be of interest, please apply with an up-to-date CV to Jessica from Next Generation Recruitment or call us on the main line at 016629120.

Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical, and Operation positions (permanent, contract, and temporary). All applications are handled in strict confidence.

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