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Base pay range
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Overview
About your new employer: A global leader in the design and manufacture of packaging and delivery systems for injectable drugs and healthcare products. The company is dedicated to improving patient health by providing innovative solutions that enhance the safety and effectiveness of pharmaceuticals.
About your new job as: Note this is a 12 month FTC. In this role, you will be responsible for developing new technologies and supporting existing ones to enhance production, quality, profitability, and safety. You will take ownership of planning, scheduling, and executing projects, while ensuring progress is communicated in line with agreed timelines. In addition, you will manage or assist with facility expansions and modifications.
Responsibilities
* Support the development of new and existing technologies, as well as production lines, to improve quality, profitability, and safety
* Plan, execute, and document project assignments in line with agreed timelines, goals, and governance policies/procedures
* Ensure all technical and customer requirements for assigned projects are achieved
* Prepare, update, and maintain validation and project management documentation
* Participate in regular project reviews with project teams and management
* Produce design work such as layouts, sketches, and concepts for projects and/or plant layouts
* Review and/or develop engineering change requests for modifications to processes, equipment, and facilities
* Troubleshoot and repair automation systems as required
* Assess and maintain machine safety systems to protect employees operating automation equipment
* Monitor production data to ensure automation lines achieve targeted output and OEE
* Maintain product quality by ensuring proper operation and upkeep of all automation systems
* Provide prompt updates to shift leaders and program managers regarding downtime or maintenance issues
* Liaise daily with the Engineering Manager and shift support staff
* Adhere to all regulations, policies, work procedures, instructions, and safety standards
* Perform additional duties as assigned by management
* Demonstrate consistent, reliable, and punctual attendance
* Work with automation systems such as assembly machines/fixtures, label applicators, robots, end-of-arm tooling, separators, test equipment, and any other equipment as assigned
Qualifications
* Associate’s Degree in a relevant Engineering discipline (required)
* Bachelor’s Degree in a relevant Engineering discipline (preferred)
* At least 3 years’ experience in the medical device or other regulated industry (required)
* Minimum 3 years’ experience supporting technical project management (preferred)
* Background in medical devices or pharmaceuticals is an advantage
* Knowledge of quality system requirements, FDA Quality System Regulations, cGMP, and relevant ISO standards
What’s on offer?
* Full time permanent position
* Bonus
* Pension and healthcare
What’s next?
* Apply now by clicking “Apply Now” or email pkiely@sigmar.ie
* Or if the job isn’t quite right but you are looking for something similar, please get in touch.
Why apply through Sigmar?
* We’ll help manage your job hunt, strengthen your interview skills, and tidy up your CV.
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