Verification Engineer Nights

We are hiring a Verification Engineer for a Pharmaceutical manufacturing client near the Kalamazoo area (per diem is available for candidates living 100+ miles from the Kalamazoo area). The Verification Engineer will support project activities to support equipment start-up and verification of our COVID19 vaccine formulation and freeze dry facilities. ROLE RESPONSIBILITIES:Provide 24x7x365 project support of our automation systems, formulation equipment and formulation facilities in our COVID19 vaccine formulation and freeze facilitiesPerform verification and automation activities to support equipment start-up and verification of our COVID19 vaccine formulation and freeze dry facilities. This includes documentation development, change control initiation, and approval routing.Follow standard operating procedures and standards in a highly regulated environment.GMP verification protocol generation and execution.Develop new and follow existing standard operating procedures and programming guidelines.Design, develop, deploy and test our automated processes, systems and equipment. Contribute substantially to the interpretation of results and the design of subsequent activities.Maintain and support automation computing infrastructure.Adhere to safe work practices and develop standard operating procedures and system support documentation. REQUIREMENTS: Minimum 3 years related verification and/or automation experience and proven background leading, training and teaching teams of verification engineers to execute their work in aseptic environments including formulation, filling, and/or freeze drying. Preferred working experience programming/using PLCs (Siemens PLC, Allen Bradley PLC, Staubli Robots, iFix, FTBatch, PlantPAX (Allen Bradley), FTView ME, & FT View SE systems, etc.) High School Diploma (or GED) required. Associates/Bachelors in engineering or technology related field preferred Understanding of systems architecture and operations, and related components1 year verification experience in a GMP environment strongly preferred.

Created: 2021-11-29