Careers

 Role Purpose:   Our client is a world leading Healthcare provider and they are looking for a Research & Design Engineer to join their team. The role will include supporting both product development & process development activities.   Duties:   Support new produce/process validations. Design, execute, and analyze experiments. Support existing manufacturing processes, quality improvements

Role Summary:   Play a pivotal role in an established engineering design team. The successful candidate will ensure that all design activities are carried out to meet with the Client Brief/ Scope of Appointment, and any subsequent design changes. Candidates should be an experienced Piping Designer with a minimum of 5 years’ experience with process

Role Summary:   We are currently recruiting for a Senior Process Engineer to join our Process Department in our thriving Cork office. Delivery of projects from concept through to full detail design stages. Activity planning, work scheduling, assigning responsibilities to the team, and ensuring deliverables can be met.   Core Duties and Responsibilities:   Lead the

Role Summary:   An exciting opportunity has arisen for a motivated Project Engineer with a leading pharmaceutical company in Tipperary The role of Project Engineer with Construction Supervisor Experience supporting site Capital & Expense projects. Reporting to the Site Projects Lead, the incumbent will work within the overall site portfolio of projects. The role is

Role Summary:   As part of a significant expansion an exciting opportunity has come to join the Validation team to transition from a project phase to a fully operational facility delivering life-saving products to patients. Each role will be involved in the project from the vendor Factory Acceptance Test (FAT), at the earliest, through to

Role Summary:   The successful Electrical Engineer will be responsible for the design, implementation and handover of multidisciplinary engineering projects. This role can be based in our Cork or Kilkenny office.   Core Duties and Responsibilities:   Management of the design, implementation and handover of multi-disciplinary engineering projects; focusing on electrical requirements, utilities, automation and

Role Summary:   The successful candidate will provide operational process support and expertise to the IPT to manufacture quality pharmaceutical products in accordance to meeting the organizational priorities of: Compliance, Supply, Strategy and Profit Plan. You will work in an environment focused on collaboration, coaching and facilitating to provide engineering solutions to the IPT team

Role Summary:   Reporting to the Automation Lead, responsible as Automation SME for project to re-write Automation Specification to standard and analyse and close any resulting gaps This candidate will be required to work closely with the Automation dept & the CSV team responsible for the project   Core Duties and Responsibilities:   Develop and/or

Role Summary:   This position will be responsible for qualification of analytical methodology for product pipeline .This role extends to implementing analytical methodology in to the Analytical, Biochemistry/Cell Biology, Micro Laboratories within QC and Manufacturing and including but not limited to cutting edge PAT/ Rapid Testing Methodology   Core Duties and Responsibilities:   Act as

Role Summary:   The CSV Engineer will be responsible for delivery of Automation and IT scope on one or more projects in the portfolio of capital projects. This candidate will be required to work closely with the teams responsible for the full Automation and IT scope and with vendors / partners with responsibility for delivery

Role Summary:   The Quality Specialist will support QRM and compliance activities as required, in collaboration with the project team. The Successful candidate will ensure that objectives are effectively achieved, consistent with MSD’s requirements to ensure compliance, safety and reliable supply to our customers.   Core Duties and Responsibilities:   Lead the QRM activities required

Role Summary:   This role will be responsible for supporting the Quality Systems Department in the management of the site GMP documentation, and in supporting the Quality Assurance functions in various administrative duties. Ensure that objectives are effectively achieved, consistent with the company requirements to ensure compliance, safety and reliable supply to our customers  

Role Purpose:   We are recruiting an Inspection Readiness, Senior Specialist (Compliance) contract position to join an existing Quality team on site.   Duties:   Support the implementation of the Inspection Readiness Program on-site. Support Compliance direction for the site by ensuring adherence to divisional policies and guidelines as well as applicable Regulatory Requirements. Lead

Role Summary:   The successful candidate will provide in-line technical support to ensure the continued manufacture and supply of quality pharmaceutical products in meeting the company priorities of: Compliance, Supply, Strategy and Profit Plan. You will be responsible for all aspects of method and equipment validation, assisting in the effective and efficient running of the