A Process Engineer solves problems related to the manufacturing and use of products, including chemicals, fuel, food, and clothing. Designs new products, improves existing ones, or develops new processes for better use of existing materials. May specialize in a chemical engineering process, such as making plastics, or in an industry such as health care.
We are seeking an experienced Process Engineer with a strong background in Oral Solid Dosage (OSD) pharmaceutical manufacturing to support a CAPEX project at our Maple Grove, MN facility. The ideal candidate will have expertise in granulation, mixing, packaging, equipment implementation, and process optimization within GMP-regulated pharmaceutical environments. Experience working with A&E (Architectural & Engineering) firms on capital projects is highly preferred. Key Responsibilities Support process engineering activities for Oral Solid Dosage manufacturing operations. Lead or support CAPEX projects involving process equipment selection, installation, commissioning, and qualification. Collaborate with A&E firms on facility design, process layouts, utilities, and equipment integration. Provide technical expertise for granulation, blending, mixing, and downstream packaging processes. Support equipment installation, FAT/SAT, startup, troubleshooting, and process optimization. Ensure manufacturing processes comply with GMP, safety, and quality requirements. Participate in risk assessments, process improvements, and technology transfers. Work closely with Manufacturing, Validation, Quality, Engineering, and EHS teams. Develop and review engineering documentation, SOPs, and technical reports. Required Qualifications Bachelor's degree in Chemical Engineering, Mechanical Engineering, Pharmaceutical Engineering, or related discipline. 5+ years of Process Engineering experience within the pharmaceutical industry. Strong experience with Oral Solid Dosage (OSD) manufacturing processes.
Hands-on experience with:
Granulation High-shear mixing Blending Packaging operations Experience supporting CAPEX projects from design through implementation. Experience working with Architectural & Engineering (A&E) firms. Strong knowledge of GMP manufacturing practices. Preferred Qualifications Experience deploying Glatt High-Shear Mixers (VG-600 or similar). Experience with Gerteis Macro-Pactor or similar roller compaction equipment. Experience processing potent compounds and understanding containment strategies. Knowledge of EHS controls for highly potent pharmaceutical manufacturing. Experience with downstream packaging systems. Experience with equipment commissioning, qualification, and startup. Strong troubleshooting and continuous improvement skills.
