Senior Lead Recruiter - NextGen International Staffing, EMEA
Required Skills & Experience
* Minimum of 5 years of experience in process engineering within the pharmaceutical or biotechnology industry.
* Proven experience with digital transformation projects in a manufacturing environment.
* Knowledge/Familiarity with process knowledge management - (process data digitally transferred from sending unit: qualified, version controlled, structured).
* Expertise in Delta V, SAP, and MES systems, with a proven track record of successful system integration and automation.
* Strong knowledge of tech transfer processes and data management strategies in a pharmaceutical context.
* Knowledge of international manufacturing and regulatory standards related to pharmaceutical products and substances.
* Large molecule pharmaceutical process engineering experience.
* Bachelor's degree in Chemical Engineering, or a related field.
Job Description
We are seeking a skilled Process Engineer to support our CMC digitization initiative for a leading pharmaceutical company in Dunboyne, Ireland. The ideal candidate will have extensive experience working in pharmaceutical manufacturing environments, experience with digital transformation, and knowledge of process knowledge management systems (PKM). Technical experience with Delta V, SAP, and MES systems, as well as expertise with pharmaceutical analytical instruments, tech transfer, and data management, is a requirement. This role will be critical in optimizing our manufacturing processes through digital knowledge transfer and automation, ensuring efficiency, compliance, and data integrity.
Key Responsibilities:
* Process Optimization: Analyze current manufacturing processes and identify opportunities for process & automation improvement. Implement best practices to enhance efficiency and quality.
* System Integration and Automation: Design, implement, and maintain automation systems using Delta V, SAP, and MES to support the CMC digitization initiative. Ensure seamless integration with existing processes and systems.
* Tech Transfer: Facilitate technology transfer activities, ensuring the smooth transition of processes and data from R&D to manufacturing and site-to-site.
* Data Management: Develop and implement data management strategies to ensure accurate, secure, and accessible data across all digitized processes. Support data collection, analysis, and reporting.
* Project Collaboration: Work closely with cross-functional teams, including R&D, Quality, Regulatory Affairs, IT, and Manufacturing, to ensure alignment and support for automation initiatives.
* Compliance and Validation: Ensure all automation and digitization efforts comply with regulatory standards and quality requirements. Participate in validation and verification of automated systems.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Pharmaceutical Manufacturing
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