Current Openings
Openning : 10 Positions
Job Title: Design Verification Engineer of SOC
Skills in ASIC / FPGA verification (directed test or SystemVerilog / UVM)
Basic knowledge in design techniques Verilog or VHDL
Good knowledge of simulation flow
Good basis in scripting Python, Perl, Bash&
A good level in English, both writing and oral skills

Humanly, you have to be rigorous and have a good analytical mind, you have to enjoy working in a team and being diplomatic, in particular when you have to point out the bugs discovered.What You Need for this Position- VHDL/Verilog
- Verification Engineer
- Verilog
- FPGA Verification
- Perl
- Bash
- Verification
So, if you are a Verification Engineer-System Verilog UVM with experience, please apply today!
Openning : 20 Positions
Job Title: Validation Engineer
Skills in CQV Validation, CSV Validation Upstream and Downstream
Basic knowledge in Annex 1, Annex 15, Annex 11
A good level in English, both writing and oral skills

Addtional knowledge in ALM, E-Val, Trackwise
Humanly, you have to enjoy working in a team and being diplomatic. What You Need for this Position
So, if you are a System Validation experience, please apply today!
Openning : 10 Positions
Job Title: QA Validation Specialist
QA/Validation related position within the pharmaceutical or life-sciences industry. • Strong experience with Validation in project related activities, including Controlled Area Facilities. • Strong experience in Validation to ensure compliance to Annex 15, EU regulations and applicable US FDA Guidelines. • Knowledge of/experience with aseptic processing and biologicals. • Knowledge and understanding of EU and US cGMP regulations with respect to the validation, production and testing of pharmaceutical and/or biological products. • Track record of utilising Risk Based Approaches to Qualification / Validation activities. • Strong track record of identifying, escalating and correcting compliance issues and implementing process improvements. • Training Material development and deployment

The QA Validation engineer will play a key role as part of the team providing hands on QA technical support and oversight to Qualification and Validation activities of the Manufacturing facility and QC Laboratories, ensuring that processes and equipment are appropriately validated and qualified in accordance with applicable Irish, EU and FDA regulations and our clients QMS.

Openning : 10 Positions
Job Title: QA CSV Validation Specialist
Responsibilities: Update the Validation, Qualification Master Plan associated with the CSV activities in accordance with the QA validation equipment. Review and approve the Qualification and Validation protocols and rapports emitted to give the assurance they are compliance with the current regulation for the CSV aspects. Review and approve the operational documentation for the projects Participate to deployment of Data Integrity program Ensure the review, challenge and approval, in compliance with GMP, Deviation, CAPA, Change Control, Risk Analysis quality system documents. Update and take appropriate measures to control the risks associated with CSV aspects for Qualification and Validation process. Participate to testing phase during an ERP deployment Review the operational documentation associate to the new ERP. QA CSV Validation Specialist Requirements: Be an expert in GMP environment. Good knowledge of quality tools (cGMP, Well acquainted with Change control/ deviation and market compliance management system) good speaking, reading, comprehension, and writing skills in English Good communication skills. Rigorous, conscientious, flexible and honest, Quality mind. Willing to bring new challenges. Good knowledge of quality tools ( cGMP, Well acquainted with Change control/ deviation and market compliance management system) Get in touch with us today to apply!

Openning : 10 Positions
Job Title: Automation Engineer
Skills : Delta V or SCADA or MES and PLC, etc
• Provide key automation support for various manufacturing systems such as DCS, MES, PLC, SCADA, and OEM systems – in a facility operating Intensified Fed Batch and Continuous Manufacturing, operating with a “Lights-Out” concept. • Support and/or Direct Continuous Improvement projects with automation review of equipment specifications, P&IDs, and System Life Cycle documentation. • Responsible for troubleshooting equipment/automation issues to improve manufacturing performance (e.g. yield improvements, etc.), changes to support new products, and maintaining the automation systems in compliance with cGMP. • Support the transfer of Process Technologies from early-stage pipeline facilities and drive to GMP Operational Status, and support line of sight to commercial supply. • Perform automation change controls with guidance from Sr. Automation Engineer or Automation Lead to ensure that changes are raised and closed on time following the required quality standards. • Supporting the qualification of new systems. Write, review, and/or execute test documents. • Effectively collaborates with cross functional peers. • Participate and actively support Digital Transformation initiatives involving system integrations, data connectivity, validation methods and value-based optimization of manufacturing via process control system.