Description:The facility is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments. When you work here you will join a global network of manufacturing professionals focused on several key, final production processes, including sterile formulation, filling, inspection, device assembly and packaging.BA/BS in engineering/related field or equivalent combination of experience & education requiredMinimum 9 years of engineering experience in process-based manufacturing, utility &/or packaging systems requiredExperience troubleshooting automation & control systems & batch processes requiredExperience working in a pharmaceutical manufacturing environment requiredKnowledgeable in SCADA (i.e. iFix, Ignition, FactoryTalk), PLC & HMI (Rockwell/AB, Siemens, etc.), historian/data collections requiredProgramming & configuration of process control systems requiredWindows based operating systems & associated applications requiredSystem interfacing & integration & user access management requiredVirtual machines/environments (preferably VMWare) preferredKnowledgeable in Oracle, MS SQL preferredIT competencies to an understanding level: domain, networking, firewall, group policies/permissions, system backup & restore preferredKnowledgeable in MES (PAS-X, etc.); MS SQL, databases preferredProven expertise in planning/organization & project execution requiredStrong in following up on results & revising work plans requiredSkills:Continuous improvement, Siemens, plc programming, automation, programming, troubleshooting, allen bradley plc, GMP, pharma, controls engineering, design, siemens plc, electrical engineering, SCADA, hmi, allen-bradley, packaging line, clean utilitesTop Skills Details:Continuous improvement,Siemens,plc programming,automation,programming,troubleshooting,allen bradley plcAdditional Skills & Qualifications:Other Requirements: Ability to work in an open office environment with the possibility of frequent distraction Ability to work the hours necessary to support a 24/7 continuous manufacturing operation Ability to adjust schedule to work with colleagues in other time zones, if necessary Ability to travel internationally & domestically, as necessary Routinely operates & inspects manufacturing equipment using handsExperience Level:Expert LevelAbout Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.