Process Controls Validation Engineer 1

The Process Control Validation Engineer will be the primary engineer for Cleanroom and Clean Environment Qualifications. Support equipment and analytical instrument qualifications a well as the manufacturing of pharmaceuticals in a cGMP manufacturing facility. Specific Responsibilities include: Develop, review, and approve validation testing and protocols for cleanrooms and environments in conjunction with other validation team membersWork cross-functionally with Manufacturing, Project Management, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, Information Technology (IT), and MaintenanceDevelop, review, and approve equipment/analytical instrument related Engineering StudiesAnalyze results from Engineering Studies to make conclusions and recommendations Design documents for facilities/equipment/analytical instrumentsEvaluated the impact of proposed changes on the validated state of facilities/equipment/analytical instrumentsCreate validation schedules, coordinate execution efforts with contractors, production operators, production engineers, customers and quality assurance staff membersAbility to work through a Management of Change system to determine the impact of proposed changes to the qualification status of equipment, software, or facilitiesSound understanding of Quality Risk Management concepts Who You Are: Minimum Qualifications:  Bachelor's Degree in Electrical Engineering, Chemical Engineering, or other Engineering discipline OR Biology, Chemistry, or other Life Science discipline 1+ years' quality support experience in a cGMP pharmaceutical setting (such as deviation/CAPA support, root cause and risk assessment, and/or periodic review experience) Preferred Qualifications: 3+ years' quality support experience in a cGMP pharmaceutical setting2+ years' of cleanroom or clean environment operation experience2+ years' of validation engineering include equipment, process controls, process, cleaning, or temperature unitKnowledge of pharmaceutical standards, rules and guidance (e.g. FDA, EU, ISO, ISPE, etc.)Ability to utilize GDP during document creation and reviewComfortable in a fast-paced environment with the ability to adjust to changing priorities. Flexible and accountableAwareness of EU Annex 1 Guide (Issued Year 2023)