Validation Engineer

Description: Integration (Process Validation) Engineer Medical Device Contract Manufacturer - Flexible Films & Packaging Position Summary The Integration (Process Validation) Engineer is responsible for leading and supporting process validation and manufacturing integration activities for medical device packaging, flexible film converting, and related manufacturing processes. This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA

Job Summary: We are seeking an experienced Validation Engineer to support system-level Verification & Validation (V&V) activities for medical device products. The role involves planning and executing V&V activities, developing and executing validation protocols, supporting design verification, and ensuring compliance with FDA, ISO 13485, and internal quality system requirements. Experience with infusion pump systems or similar electromechanical medical devices is preferred. Roles & Responsibilit

SW Validation Engineer Job Description & Skill Requirement: Strong understanding of BMS Architecture and Software Qualification Process. Good exposure to ASPICE processes. Proficient in BMS component testing and debugging methodologies. Experienced with MATLAB, HiL Systems, and Vector Toolchain. Good knowledge of Cybersecurity and Functional Safety aspects. Hands-on CAPL experience and tool development for software validation using CAPL and Python. Excellent team and customer handling skills.

Joining the PHC Group means becoming a vital player in one of the world's foremost producers and suppliers of top-tier laboratory equipment. Operating in the dynamic biomedical and diagnostics sectors, we cater to a diverse and expanding range of life science facilities. Our products are essential tools for researchers and professionals in pharmaceuticals, biotechnology, and healthcare, making a meaningful impact on advancements in these fields. Your role with us will be an integral part of this