Description:
Kelly Services is currently recruiting a Senior Equipment Engineer for our Global Biopharmaceutical client in south Co. Dublin.
The position will report to the Engineering Manager for Inspection and Packaging Engineering support group and is responsible for scoping and executing technical projects supporting manufacturing within Inspection, Labelling and Packaging areas.
This is a 1 year contract initially with excellent rate and opportunities available.
Key Responsibilities
- Working with various stakeholders, to scope projects and ensure requirements are satisfied. Project management and execution of assigned projects including project prioritization, resources management, status management and external communication.
- Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues prior to qualification & start-up
- Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment.
- Ability to translate strategic/emerging technology solutions into pragmatic executable plans
- Development and management of change controls
- Participate as a member of multidisciplinary site and multisite teams
- Development of detailed specifications, engineering documents, protocols and standard operating procedures
- Work in a collaborative manner within the Process Teams structure and contributes to Root Cause Investigations and Cross Functional Investigations.
- Works in a collaborative manner with the System Owners, Maintenance Supervisors & Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits.
- Perform all tasks with due care and attention ensuring compliance with Good Manufacturing Practices and company requirements, policies and procedures
- Support a safe working environment by complying with environmental health/safety practice, rules and regulations
Knowledge, Experience And Skills
- Bachelor's Degree in Engineering (Mechanical, Electrical or Chemical) or Relevant Experience
- 5+ years engineering experience, preferably in the biotechnology industry / aseptic pharmaceutical environment or Automated Inspection and/or Automated Device Assembly, Labelling and Ancillary processes.
- Process development or technology transfer experience preferred.
- Proven project management experience.
- Strong mechanical capability with hands on experience in a technical role within a high-volume manufacturing environment, is advantageous
- Demonstrated experience in a GDP Compliant environment.
- Experience in MS Office, MS Project, Change Control & Document Management Systems
- Proven ability working cross functionally, delivering technical solutions and implementing improvements.
- Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results
- Technical report writing and communication/presentation skills
- Data driven decision maker
- Ability to work to tight deadlines in a fast-moving environment