For our client, an international company based in Neuchatel, we are looking for a Manufacturing Engineer .
General Information:
Workplace: Neuchatel
Contract: Temporary
Start date: 01.02.2025
End date: 31.07.2025
Workload: 100%
Please note French fluency is mandatory for this position.
Tasks and Responsibilities:
Within the Manufacturing department, reporting to the Deviation Manager, the primary mission for the Manufacturing Engineer is to support the manufacturing operations to meet their goals in terms of quality and productivity. He/she specifically provides technical expertise needed to investigate deviations related to the manufacturing process and acts as a catalyst for continuous improvement. Main responsibilities include:
Deviation Management: Initiate and manage deviations within the framework of production events and quality systems in a timely manner.
Perform evaluations related to impact on concerned equipment/product/material with the support of relevant Subject Matter Experts (SME).
Conduct investigations of varying complexity/severity using root cause analysis tools (e.g., DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.).
Lead multi-disciplinary investigation teams and associated workshops as appropriate.
Conduct interviews related to human factors in deviations.
Collect/compile data and write investigation summary reports.
Define robust corrective and preventive actions.
Identify relevant criteria to monitor efficacy of CAPA and ensure follow-up until closure of the record.
Provide technical expertise on manufacturing processes relevant to sub-group (PUT).
Deviation Report Out: Proactive and autonomous follow-up of deviations under responsibility to ensure timely completion of each step.
Propose technical and organizational solutions.
Accurate reporting to relevant follow-up platforms.
Ensure report out of findings/issues to high management and other sites.
Act as SME during internal and external audits.
Continuous Improvement: Identify opportunities and propose ideas for improvement, in and out of deviations scope.
Lead or participate in manufacturing process continuous improvement initiatives.
Your Profile:
Bachelor/Master in Engineering and 3-5 years of experience within a biotech/pharmaceutical manufacturing environment (Process Operations or Quality).
Technical knowledge of biotechnological processes (USP and/or DSP).
Demonstrated experience in deviation management including use of Six Sigma tools (e.g., DMAIC, Is/Is Not, Cause & Effect Diagram, 5M, Contradiction Matrix, etc.).
Experience of Quality/Compliance requirements within cGMP manufacturing environment.
Written and oral proficiency in French and English.
Experience in computerized/automated/QMS systems (e.g., Trackwise, ERP, Veeva Vault).
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