JOB OFFER

JOB DETAILS

Title:
Pharmaceutical Device Technician
Location:
Sligo
Job Type:
Full-Time

Pharmaceutical Device Technician

GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world’s largest life science & technology companies who entrust in us to deliver their most strategic and important projects with our technically strong personnel ensuring all important activities meet both current requirements and client’s needs. We have multiple projects that we support, and we are looking to add to our team, we are interested in talking to you if you fit the criteria outlined below:

Pharmaceutical Device Technician

Job Summary:

To work as a team member in production/operations areas in line with all safety, regulatory and organizational requirements.  Preparing equipment, work areas and materials and ensuring/verifying readiness of manufacturing operations

 

Responsibilities:

  • Preparation and operation of moulding and ancillary equipment.
  • Preparation and operation of automated assembly and ancillary equipment.
  • Preparation and operation of Pad Printing and ancillary equipment.
  • Preparation and operation of manual assembly and ancillary equipment.
  • Troubleshooting day to day manufacturing issues which may impact on efficiencies, safety or quality.
  • Completion of quality checks and achieving production quality targets.
  • Supplying materials to the operations and equipment in a timely and safe manner.
  • Responsible for labeling and packing of components and finished products.
  • Operating of Coordinate measuring equipment, and other advanced metrology equipment.
  • Operate fully automated and complex computer-controlled systems, including robotic and vision system technology.
  • Participate in divisional project team for New Product Introduction and Improvement Projects.
  • Resetting equipment as necessary to ensure the manufacture of quality components.
  • Team coordination to maximize the effectiveness of all of the team members.
  • Documentation of all activities in line with GMP requirements.
  • Cross training within the team and training of new members.
  • Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
  • Execution of routine manufacturing documentation, commissioning and validation protocols on an ongoing basis.
  • Ensuring compliance with the Quality, Regulatory, GMP requirements and adherence to all policies and relevant legislation.
  • Ability to work on own initiative.
  • Execute manual assembly and visual inspection as required.

 

Qualifications:

Essential Requirements

  • Leaving Certificate or equivalent, desirable · or relevant work experience
  • Working knowledge of: Microsoft Office Suite beneficial.

 

 

Desired Requirements

  • 3rd level education.

 

Experience required:

Technical/Business Knowledge -Job Skills/Experience Required

  • Minimum 1 year of experience in regulated manufacturing environment required.

Supervision Received

The position will report directly to the shift supervisor who will ensure the goals are defined and resources available to each shift. The shift supervisor and Device Group Leader will provide the following services to the team members as required.

 

  • Direct coaching/training of members as required.
  • Clearly define individual goals.
  • Ensure adequate resources are in place.
  • Develop training plans for each individual.
  • Monitor performance, and complete performance reviews with each individual.
  • Develop a team culture with active participation from all members.

 

The Device Technician will organise the following elements of their workload:

  • Cross training within the shift and direct training of new team members as required.
  • Team management of participation in the continuous improvement activities.
  • Self-auditing of shift activities, to ensure excellence of GMP/safety and manufacturing activities.
  • Completion of all documentation and manufacturing control system transaction in line with all cGMP and operational requirements.
  • Coordination between shift teams to ensure excellence in GMP/safety and manufacturing activities.

 

Supervision Provided

  • No direct reports
  • Maintains regular contact with support functions on site, i.e. warehouse, quality, technical support, maintenance, metrology and engineering.
  • All of the manufacturing processes and instructions are confidential information.

Shift Working: The role requires working in evening and night shifts.

We offer competitive compensation packages and opportunities for professional growth in a dynamic and innovative work environment. If you are a motivated Technician seeking an exciting challenge in the biopharmaceutical industry, we encourage you to apply.

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