Junior to Mid-Level Quality Control/Validation Engineer IRELAND, IRELAND / NORTH EUROPE / FULL TIME About CAI: CAI is a 100% employee-owned company established in 1996, growing year over year to nearly 700 employees worldwide. We provide commissioning, qualification, validation, start-up, project management, and consulting services related to operational readiness in FDA regulated and other mission-critical industries. Are You Ready?: Our approach is simple: we put the clients interests first, we do not stop until it is right, and we will do whatever it takes to get there. As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally: - We act with integrity - We serve each other - We serve society - We work for our future With employee ownership, one persons success is everyones success. We work diligently to accomplish team goals. We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude. That is how we have grown exponentially. CAI agents will be exposed to cutting-edge technologies in the advanced medicine space, working alongside recognized subject matter experts. As part of our culture, we invest in YOUR future through hands-on certifications and professional training. Position Overview: We are looking for a Junior to Mid-Level Validation Engineer to join our growing operations in Ireland. This role is designed for individuals with at least 2 years of relevant experience in Validation Engineering or Quality Control. As a Junior to Mid-Level Engineer, you will work alongside senior team members, assisting in maintaining quality standards and ensuring compliance throughout all equipment qualification activities. Key Responsibilities: - Support and assist with Quality Control compliance for equipment qualification activities, ensuring adherence to safety and regulatory standards. - Help document and execute equipment qualification processes, from initial assessments to Operational Qualification (OQ), focusing on accuracy and attention to detail. - Follow established procedures and protocols for new equipment qualification to help embed quality practices within workflows. - Assist with the review and completion of Test Outlines and Procedures (TOPs), verifying alignment with quality specifications. - Support the planning and organization of commissioning materials and consumables, ensuring they meet required quality standards. - Monitor equipment qualification activities to ensure that timelines are met while maintaining high quality standards. - Assist in preparing and maintaining Qualification Summary Reports (QSRs) and related documentation to ensure compliance with quality standards. - Participate in equipment Design Evaluations, Factory Acceptance Testing (FAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), with a focus on achieving quality outcomes. - Assist in managing quality control processes related to equipment qualifications, including documentation control, change controls, and punch list tracking. - Collaborate with project contractors and equipment vendors to perform and verify tests, ensuring quality control is upheld. - Provide support for quality assurance tasks throughout the equipment qualification process, ensuring consistent quality standards are maintained. Position Requirements: - BS or MS in a relevant science or engineering field, or equivalent experience. - 2+ years of industry-related experience in a similar role. - Strong oral and written communication skills, with a focus on clear documentation and reporting. - Strong problem-solving skills with a focus on Quality Control. - Customer-service oriented and able to collaborate well with internal teams and external vendors. - Familiarity with life science manufacturing processes such as biotech, aseptic fill/finish, oral solid dose (OSD), and gene therapy, or equivalent experience. - Willing and able to travel domestically and internationally, if required. Skills: Quality Control QC Technican Equipment Validation Life Science Bio-Pharma Pharmaceutical Manufacturing Benefits: Pension Fund Medical Aid / Health Care Dental Care Income Protection Group Life Assurance
Junior to Mid-Level Quality Control/Validation Engineer IRELAND, IRELAND / NORTH EUROPE / FULL TIME About CAI: CAI is a 100% employee-owned company established in 1996, growing year over year to nearly 700 employees worldwide. We provide commissioning, qualification, validation, start-up, project management, and consulting services related to operational readiness in FDA regulated and other mission-critical industries. Are You Ready?: Our approach is simple: we put the clients interests first, we do not stop until it is right, and we will do whatever it takes to get there. As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally: - We act with integrity - We serve each other - We serve society - We work for our future With employee ownership, one persons success is everyones success. We work diligently to accomplish team goals. We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude. That is how we have grown exponentially. CAI agents will be exposed to cutting-edge technologies in the advanced medicine space, working alongside recognized subject matter experts. As part of our culture, we invest in YOUR future through hands-on certifications and professional training. Position Overview: We are looking for a Junior to Mid-Level Validation Engineer to join our growing operations in Ireland. This role is designed for individuals with at least 2 years of relevant experience in Validation Engineering or Quality Control. As a Junior to Mid-Level Engineer, you will work alongside senior team members, assisting in maintaining quality standards and ensuring compliance throughout all equipment qualification activities. Key Responsibilities: - Support and assist with Quality Control compliance for equipment qualification activities, ensuring adherence to safety and regulatory standards. - Help document and execute equipment qualification processes, from initial assessments to Operational Qualification (OQ), focusing on accuracy and attention to detail. - Follow established procedures and protocols for new equipment qualification to help embed quality practices within workflows. - Assist with the review and completion of Test Outlines and Procedures (TOPs), verifying alignment with quality specifications. - Support the planning and organization of commissioning materials and consumables, ensuring they meet required quality standards. - Monitor equipment qualification activities to ensure that timelines are met while maintaining high quality standards. - Assist in preparing and maintaining Qualification Summary Reports (QSRs) and related documentation to ensure compliance with quality standards. - Participate in equipment Design Evaluations, Factory Acceptance Testing (FAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), with a focus on achieving quality outcomes. - Assist in managing quality control processes related to equipment qualifications, including documentation control, change controls, and punch list tracking. - Collaborate with project contractors and equipment vendors to perform and verify tests, ensuring quality control is upheld. - Provide support for quality assurance tasks throughout the equipment qualification process, ensuring consistent quality standards are maintained. Position Requirements: - BS or MS in a relevant science or engineering field, or equivalent experience. - 2+ years of industry-related experience in a similar role. - Strong oral and written communication skills, with a focus on clear documentation and reporting. - Strong problem-solving skills with a focus on Quality Control. - Customer-service oriented and able to collaborate well with internal teams and external vendors. - Familiarity with life science manufacturing processes such as biotech, aseptic fill/finish, oral solid dose (OSD), and gene therapy, or equivalent experience. - Willing and able to travel domestically and internationally, if required. Skills: Quality Control QC Technican Equipment Validation Life Science Bio-Pharma Pharmaceutical Manufacturing Cleaning Validation Benefits: Pension Fund Medical Aid / Health Care Dental Care Income Protection Group Life Assurance
Senior Validation Engineer Location: Ireland / Germany / Italy / Netherlands Full-Time Salary: €50,000 €75,000 (depending on experience) Are you a skilled Validation Engineer and ready to relocate? We are looking for professionals to join high-impact biopharmaceutical projects in Ireland, Germany, Italy, and the Netherlands. This opportunity is ideal for experienced engineers seeking career progression in an international environment. About CAI CAI is a global consulting company founded in 1996, now with nearly 700 employees worldwide. We provide commissioning, qualification, validation (CQV), startup, and project management services for FDA-regulated and other mission-critical industries. We focus on Acting with integrity Supporting clients, colleagues, and communities Delivering future-focused solutions Valuing teamwork over individual ego Position Overview You will ensure the highest quality standards during equipment qualification processes and provide technical guidance across validation activities. The role requires experience, leadership, and a strong understanding of regulatory and industry best practices. Key Responsibilities Lead and support quality control for equipment qualification Oversee IQ, OQ, PQ activities and documentation Mentor junior staff and promote best practices Review and complete validation protocols (TOPs, QSRs) Ensure proper planning of materials and consumables Maintain documentation quality and regulatory compliance Coordinate with vendors and contractors to ensure standards are met Participate in FAT, SAT, and other qualification phases Drive continuous improvement in validation procedures Requirements Bachelors or Masters in Science, Engineering, or related field Minimum 5 years of experience in validation, QC, or commissioning in pharma/biotech Advanced English proficiency (C1 Cambridge level or higher) Strong written and verbal communication skills Solid understanding of GMP and relevant regulatory frameworks Experience with aseptic fill/finish, OSD, gene therapy, or biotech processes Willingness and ability to relocate to Ireland, Germany, Italy, or the Netherlands What We Offer Competitive salary: €50,000 €75,000 Relocation package: travel support, temporary housing, and financial assistance Private health insurance and life cover 22 days annual leave plus 10 public holidays Paid overtime or comp time Company phone or reimbursement Pension contributions and support for professional memberships Ongoing training and development opportunities Why CAI? Youll work in a supportive and collaborative environment on innovative life sciences projects across Europe. CAI is committed to your growth through hands-on experience, certification support, and career development in a dynamic, international setting. Apply now and take the next step in your validation engineering career with CAI. Skills: Quality Control QC Technican Equipment Validation Life Science Bio-Pharma Pharmaceutical Manufacturing CSV Benefits: Pension Fund Medical Aid / Health Care Dental Care Income Protection Group Life Assurance
