GerTEK Project Management and Technical Services Hiring for Manufacturing Technician Job at Ireland , Ireland Full Time

GerTEK Project Management & Technical Services are an outsourced technical services provider delivering worldwide contract and permanent staffing solutions. We are accepting applications for our Manufacturing Technician role based in Sligo.

Job Responsibilities

• To provide an engineering service to support site pharma operations to maximize availability and reliability of pharma equipment to produce biologics.
• To ensure continual compliance with the policies relating to Personnel, Quality, Engineering, Safety and Finance. Primary Function To work as a team member to support engineering in pharma operations in line with all safety, regulatory and organizational requirements.
• Participating in design and process project conversations to ensure reliability by design is built in prior to equipment arrival.
• Owning and preparing, preventative and predictive maintenance for new pharma equipment being installed and approval of these procedures on Maximo.
• Completion and documentation of PM’s and pDM’s on manufacturing equipment into Maximo.
• Owning and ensuring that commissioning spare parts are received and catalogued in Maximo.
• Active Participation in Factory Acceptance testing, Site Acceptance Testing, and commissioning and qualification of equipment.
• Review and approve process related commissioning, qualification and validation protocols for completeness and accuracy. Execute protocols in a timely basis to meet the project schedule requirements
• Liaising with operations, quality, and technical operations to ensure equipment and process performance is maximized.
• To liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining troubleshooting and installing/commissioning equipment.
• Completion of instrument calibration as per schedule.
• Take ownership of the site’s Predictive Maintenance program, through managing and developing the outsourced condition monitoring contracts, implementing recommendations, and tracking to closure
• Implementation of equipment/process upgrade in an environment of continuous improvement.

Education & Key requirements

• Degree educated in engineering or Trade qualification
• 3 years plus experience in a highly regulated manufacturing (Pharma/Biologics/Medical Device) environment.
• Adheres to and follows all procedures policies and guidelines ensuring compliance with cGMP and ISO/FDA regulations and company policies, procedures, and guidelines.
• Strong interpersonal skills

#INDHP

Job Type: Full-time

Schedule:

• Day shift