Join PBE Expert Inc as an Intermediate Process Engineer to enhance manufacturing processes in Pharmaceuticals and Biotechnology. This role offers flexible hours and international project opportunities.
As an Intermediate Process Engineer at PBE Expert Inc, you will work under experienced professionals, aiding in the design, validation, and compliance audits of pharmaceutical systems. Your role will involve working with URS, PFD, and P&ID standards, ensuring that products meet regulatory guidelines. Experience in project management is an advantage as you integrate into their dynamic team.
Key Responsibilities:
• Assist in process design and layout specifications
• Support GMP compliance audits and reviews
• Aid in equipment commissioning and qualification
• Contribute to validation processes for manufacturing
• Collaborate on commercial development projects
Requirements:
• 5 years of Clean Process Design experience
• Familiarity with ASME BPE and GAMP stand...