Production Technician

IDEX; Shannon; On-site; EUR 45,000 - 55,000; Full time

Job summary

IDEX Shannon onsite is seeking a Production Technician to assemble biopharma equipment (MUT/SUT) and support testing and validation in a regulated environment.

You will read electrical schematics, document results, and ensure quality and safety standards are met while collaborating with Engineering, QA, and Operations teams.

Qualifications

• Essential technical qualification in Mechanical Engineering, Manufacturing, Mechatronics, Biotechnology Equipment, or a related discipline.
• Previous experience in a manufacturing, assembly, or production environment.
• Experience working with mechanical assemblies, tools, measuring equipment, and technical drawings.
• Computer literacy and experience using production or ERP systems.
• Strong documentation and record-keeping skills.

Responsibilities

• Manufacturing & Assembly: Assemble biopharma production pump, MUT systems, and SUT assemblies per drawings and quality standards.
• Testing & Validation Support: Conduct functional and mechanical testing and assist validation activities.
• Electrical & Control Systems: Read schematics, upload software to PLC/HMI, support commissioning.
• Quality & Compliance: Ensure GMP/ISO compliance, complete records, maintain traceability.
• Documentation & Systems: Record results in ERP/MES, maintain revision-controlled records.
• Continuous Improvement: Identify efficiency and quality improvements, support Lean initiatives.
• Cross-Functional Support: Collaborate with Engineering, QA, Supply Chain, and Operations.
• Health, Safety & Environment: Follow HSE policies and maintain safe workplaces.

Job description

If you’re looking for a special place to build or grow your career, you’ve found it. Whether you’re an experienced professional, a recent college graduate or somewhere in between, IDEX is a place where you can apply your existing skills and learn new ones in an environment where you can make an impact. With interesting opportunities in engineering, marketing, sales, supply chain, operations, HR, finance, and more across more than 40 diverse businesses around the globe, chances are, we have something special for you.

SUMMARY: Shannon - Onsite

The Production Technician is responsible for the assembly, testing, validation support, and documentation of biopharmaceutical processing equipment associated with Multi-Use Technology (MUT) and Single-Use Technology (SUT) systems. Working within a regulated manufacturing environment, the role ensures products are manufactured, tested, and documented to the highest quality and compliance standards.

PRIMARY DUTIES AND RESPONSIBILITIES:

Manufacturing & Assembly

• Manufacturing & Assembly Assemble biopharma production pump, Multi Use Technology (MUT) systems, and Single-Use Technology (SUT) assemblies in accordance with engineering drawings, work instructions, and quality standards.
• Perform mechanical assembly, fitting, tubing installation, component integration, and final product configuration.
• Conduct visual inspections throughout the assembly process to ensure compliance with customer and regulatory requirements.
• Follow standard operating procedures (SOPs), manufacturing instructions, and Good Documentation Practices (GDP).

Testing & Validation Support

• Testing & Validation Support Perform functional, mechanical, and operational testing on completed assemblies and systems.
• Carry out Production Testing, Installation Qualification, Operational Qualification, and Performance Qualification activities as required.
• Utilize measuring and testing equipment to verify product specifications and performance.
• Assist with troubleshooting and root‑cause investigations of assembly or testing failures.

Electrical & Control Systems

• Electrical & Control Systems Read and interpret electrical schematics, wiring diagrams, panel layouts, and control system documentation.
• Upload approved software and configuration files to PLC and HMI systems as required during manufacturing and testing activities.
• Support commissioning activities through verification of electrical and control system functionality.
• Perform basic fault finding and troubleshooting of electrical components including power supplies, sensors, instrumentation, actuators, PLCs, HMIs, and communication networks.
• Identify, diagnose, and report electrical or control system issues, supporting corrective actions and resolution activities.
• Utilize electrical test equipment as required to verify wiring integrity, component functionality, and system operation.
• Ensure all electrical work is performed in accordance with company procedures, engineering requirements, and applicable safety standards.

Quality & Compliance

• Quality & Compliance Ensure all manufacturing activities are completed in accordance with good manufacturing practices, ISO, and company quality requirements.
• Complete production records, test reports, validation documentation, and traceability records accurately and on time.
• Maintain component and material traceability throughout manufacturing processes.
• Participate in quality investigations, non‑conformance reporting, and corrective and preventive action (CAPA) activities as required.
• Promote a strong quality culture and Right First‑Time approach.

Documentation & Systems

• Documentation & Systems Record manufacturing and testing results within ERP, MES, or other electronic systems.
• Maintain accurate production documentation and revision‑controlled records.
• Support the review and continuous improvement of manufacturing procedures and work instructions.
• Ensure compliance with data integrity and documentation standards.

Continuous Improvement

• Continuous Improvement Identify opportunities to improve manufacturing efficiency, quality, safety, and productivity.
• Participate in Lean, 5S, and continuous improvement initiatives.
• Contribute to process optimization and manufacturing best practices.
• Support new product introductions (NPI) and process validations as required.

Cross-Functional Support

• Cross-Functional Support Collaborate effectively with Engineering, Quality Assurance, Quality Control, Supply Chain, and Operations teams.
• Support inventory management, material handling, packing, shipping, and other production activities as required.
• Assist in training new team members and sharing technical knowledge and best practices.
• Support customer, supplier, and auditor visits when required.

Health, Safety & Environment

• Health, Safety & Environment Adhere to all company Health, Safety, Environmental, and Quality policies.
• Maintain a clean, organized, and safe work environment.
• Properly use personal protective equipment (PPE) and follow safe working practices.
• Participate in safety initiatives and risk assessments.

Education & Experience

Essential Technical qualification in Mechanical Engineering, Manufacturing, Mechatronics, Biotechnology Equipment, or a related discipline. Previous experience in a manufacturing, assembly, or production environment. Experience working with mechanical assemblies, tools, measuring equipment, and technical drawings. Computer literacy and experience using production or ERP systems. Strong documentation and record‑keeping skills.

Desirable Experience in biopharmaceutical, medical device, life sciences, or regulated manufacturing environments. Knowledge of Single‑Use Technology (SUT) systems and bioprocess equipment. Understanding of GMP, FDA, ISO 9001, ISO 13485, or similar quality standards. Experience supporting validation or testing activities. Lean Manufacturing or Continuous Improvement experience.

Key Competencies

• Strong mechanical aptitude and problem‑solving skills.
• Excellent attention to detail.
• Ability to work independently and within a team environment.
• Effective communication and interpersonal skills.
• Strong organizational and time‑management abilities.
• Adaptable and flexible approach to changing business needs.
• Commitment to quality, compliance, and safety.
• Results‑oriented with a continuous improvement mindset.

Compensation Information

The expected pay range for this position is 45,000 - 55,000 annually. Ultimately, in determining your pay, we may also consider your experience, and other objective job‑related factors. This position may be eligible for a bonus or other incentive plan, as well as other forms of compensation.

Are you ready to join a different kind of company where our people, our culture, and our commitments are centered around providing trusted solutions that improve lives around the world? IDEX (NYSE: IEX) is a company that has undoubtedly touched your life in some way. In fact, IDEX businesses make thousands of products that are mission‑critical components in everyday activities. Chances are the car you’re driving has a BAND‑IT® clamp holding your side airbag safely in place. If you were ever in a car accident, a Hurst Jaws of Life® rescue tool may have saved your life. If you or a family member is battling cancer, your doctor may have tested your DNA in a quest to find the best targeted medicine for you. It’s likely your DNA test was run on equipment that contains components made by our growing IDEX Health & Science team.