Join Our Clients Team – Manufacturing Engineer (1 year FTC)
Location: Servier Arklow, Co. Wicklow
Department: Operational Performance
Reporting To: Project Lead
Are you a proactive and driven engineer ready to contribute to the launch of innovative pharmaceutical products? Servier Arklow is seeking a Manufacturing Engineer to support our Operational Performance team in delivering excellence in new product introductions.
Key Responsibilities:
As a Manufacturing Engineer, you will play a vital role in ensuring smooth introduction and integration of new products into manufacturing and packaging operations. Responsibilities include:
* Supporting New Product Introduction (NPI) for manufacturing and packaging
* Developing manufacturing and cleaning recipes on production equipment
* Creating Batch Manufacturing Records, Work Instructions, and SOPs
* Conducting investigations and generating reports as required
* Ensuring production readiness and supporting trial, placebo, and validation batches
* Working cross-functionally with teams in QA, QC, Validation, Technical, Supply Chain, and Finance
* Leading problem-solving initiatives using root cause analysis
* Conducting material and equipment trials with operational and validation support
Collaboration & Teamwork:
* Work closely with Operational teams including ASL, Manufacturing, Packaging, and Supply Chain
* Participate in cross-functional project teams and contribute to business improvement initiatives
* Be adaptable and willing to support additional operational needs as they arise
️ Health, Safety, Environment & Quality:
* Ensure compliance with all GMP, safety, and environmental standards
* Actively promote a culture of quality and safety across all areas of work
What We’re Looking For:
Essential:
* Degree in Process, Mechanical, or Manufacturing Engineering
* Excellent communication, interpersonal, and project management skills
* Ability to lead initiatives and collaborate effectively across teams
* Self-starter with strong initiative and the ability to work autonomously
Desirable:
* Experience in a pharmaceutical production environment
* Validation experience and report writing/presentation skills
* Ability to manage multiple tasks and meet deadlines with high-quality outcomes
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