Please enter your email address
Our client, a leading Pharmaceutical in Sligo, is seeking a Validation Engineer on an initial 3-4 month contract with a view to long term. - Co-ordination / direction and active participation in the validation of site Equipment, Facilities, Utilities and Process in compliance with company policies, HPRA, FDA, European cGMP and GAMP standards.
The desirable quality's you might have as a validation engineer here in Carlow include; The responsibilities you will have as the validation engineer here in Carlow include; If you believe you have the right skills for this validation engineer role, please contact me. A solid background in Validation with at least 3 years validation experience.
You will be responsible for all aspects of the Cleaning Validation programs onsite at the manufacturing site in Dublin. • Co-ordinate cleaning validation site wide including worst case studies. • Co-ordinate and execute Cleaning Validation studies for NPI. • Generate Protocols / Reports / SOPs / WIs associated with validation studies.
A Validation Engineer is required by CareerWise Recruitment for our Longford based client. * Coordinate and execute process validations including preparation of protocols, data analysis and reports. * Ensure software validations for equipment and systems are completed in line with industry standards.
BMS Multi- Product Cell Culture (MPCC) Facility Cruiserath is seeking to develop the site validation department. Initially part of a project team to perform Commissioning, Qualification and Validation (CQV) to complete execution and start-up of the MPCC project in Cruiserath, Ireland.
Please enter your email address
Applications are invited for the fixed term contract (12 months) of a Lead Engineer II reporting directly to the Validation Manager. While the role will be focused on Process Validation, the candidate should be an SME in other areas of Validation. The successful applicant will be play a lead role within Alkermes, representing Validation.
The role will be focused on Process Validation, as well as being an SME in other areas of Validation. SME in Process Validation Development and execution of Validation related documents throughout the system lifecycle
Engineering Job - Validation Engineer - This is an exciting opportunity to join a diverse and innovative Medical Device manufacturing site in Cork. •The execution and completion of process, systems and equipment validations and revalidations in accordance with Validation Master Plans, schedules and Company Policy.
Role Title: Validation Engineer To engage in equipment, process and facility validations to ensure compliance with regulatory, corporate and business requirements. This includes both development and execution of the validations This would entail producing project documentation including validation and software documents
I am delighted to be assisting this lovely SME manufacturer in Shannon find a Validation Engineer to join their team. It is an exciting opportunity for an experienced validation engineer to join their our growing business. 3-5 years' experience in a validation role in either Medical Device or Pharmaceutical Industry.
This role offers a great opportunity for a suitably qualified Electronic Engineer to work on world-leading non-contact sleep and respiration technology. Testing of RST innovative algorithms for the monitoring of physiological parameters - Build on RST’s algorithm test platform for new products / new features / new use cases
The Validation Engineer will be part of a project team for the Qualification and Validation of Autoclaves and SIP systems for a Greenfield fill finish project. The Validation Engineer will have 3 plus years in Validation and prior experience with the qualification of Autoclaves.
Our client is looking for an experienced, enthusiastic and capable Validation Engineer to join their validation team in a high volume medical device manufacturer facility to support a wide range of projects. Job Title: Validation Engineer
The successful Validation Engineer will be part of a project team for the Qualification and Validation of a Greenfield fill finish facility. The Validation Engineer will have 3 plus years in Validation and prior experience with fill finish equipment. LSC are currently looking for a Validation Engineer join a Fill Finish Project in Denmark. Email: ]]>
Our client, a large medical device company in Galway are currently looking to recruit Senior Validation Engineers, Validation Engineers and Validation Technicians for their Galway site, on a contract basis. For further information on Senior Validation Engineers Galway please contact Anne Gough on 091730022 / 0860449473
CAI is looking for individuals with at least 2 years of experience in the areas of commissioning, validation, automation and quality/compliance to join our team in Europe.
A Validation engineer is required for a 12 month contract in a state of the art global health care leader based in Galway. Role: Validation Engineer Your role will be in a pharmaceutical company who currently require a validation engineer for a new project they are starting which will help save people's lives, based in Galway.
Experienced Validation Engineer required for high volume medical device manufacturing facility in Dun Laoghaire, South Dublin to work on 4 new lines. Use of (BD and Unit level) Validation Toolkits - Define validation sampling and inspection plans based on Risk Assessment - Link with Post Validation activities including closure of change control
Plans, coordinates, and participates in a compliant validation process for production automation/enterprise systems. * Lead process improvement projects to improve the validation of computerized systems * Coordinates with other departments or outside contractors/vendors to complete validation tasks.
We are seeking to recruit a validation engineer to join the R+D team based in Shannon. Minimum 5 years experience in the development of test programs for the qualification of consumer electronic products including the development of software validation testing scenarios. Support on site customer validation testing as required
Our client, a multinational healthcare manufacturing company, now seeks a Lead Validation Engineer who will be focused on Process Validation in an FDA regulated, GMP manufacturing environment.
LSC require an experienced biotech Equipment Validation Engineer to work with our Biotech client in Limerick. The Equipment Validation Engineer will be responsible for document preparation and execution activities for the initial qualification activities for biotech manufacturing equipment.
Reporting to the Quality Manager Projects, the Validation Engineer is responsible for the design and execution of validation programs and strategies to support the implementation of the Validation Master Plans. Senior Validation Documenation Engineer position available with leading Bio-Technology client based in Cork.