CIS International Jobs in United States

· SUMMARY: · The Sr. Associate Technical Engineering will provide technical engineering support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that all of the maintenance team operations and activities are maintained in comp ...

· SUMMARY: · Under limited supervision, execute advanced maintenance activities or operate assigned equipment, facility, utility, and HVAC Systems in accordance with established guidelines and operating procedures. Conduct intermediate troubleshooting and employ advanced predict ...

· Responsibilities:The Cleaning Validation Specialist (Contractor) will support the introduction of new products in a Contract Manufacturing Organization (CMO) environment. · This role is responsible for developing and executing the full cleaning validation lifecycle, including: ...

· SUMMARY: · Under general supervision, execute intermediate maintenance activities. Operate assigned equipment, facility, utility, and HVAC Systems in accordance with established guidelines and operating procedures. Conduct basic troubleshooting and employ basic predictive tech ...

· Summary · The Manufacturing Engineer is responsible for designing, developing, validating, and sustaining manufacturing processes, equipment, and systems to ensure efficient, compliant, and high-quality production. This role functions as an established individual contributor, ...

· EHS Specialist Job Description · EHS Programs and Compliance:Support a proactive, preventive safety culture by modeling safe behaviors and reinforcing expectations across site teams. · Support the site Process Safety Management (PSM) program by assisting with PHAs, MOC reviews ...

· SUMMARY: · In a full automation role the Sr. Associate Mfg Systems will provide technical engineering support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that all of the maintenance team operations and activities are ma ...

· Summary: · We are seeking candidates with a strong engineering background and hands-on experience in regulated manufacturing environments, preferably within the medical device industry. Ideal candidates will have direct experience with process validation activities including c ...

· Summary: · We are seeking candidates with a strong engineering background and hands-on experience in regulated manufacturing environments, preferably within the medical device industry. Ideal candidates will have direct experience with process validation activities including c ...

· Main Responsibilities:Lead and execute Computer System Validation (CSV) activities for Quality Information Technology systems in compliance with FDA, GxP, ISO, and global regulatory requirements. · Conduct and maintain formal validation documentation, including Validation Plan ...

· Summary: · The Project Engineer provides direct technical and operational support to Project Managers leading capital projects within a regulated medical device manufacturing environment. This role is responsible for coordinating engineering activities, supporting equipment an ...

· SUMMARY: · Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies advanced and diverse engineering princip ...