B.S. or M.S. in Mechanical Engineering or equivalent education
Proficient in SolidWorks and other 3D CAD software
Strong mechanical, analytical, and technical skills
Preferred experience in mentoring junior engineers
Extensive background in equipment/system engineering design
Familiarity with GMP standards is desirable
Experience in a relevant manufacturing environment is a plus
Responsibilities
Collaborate with cross-functional teams to design 3D pharmaceutical processing equipment
Modify and design equipment for GMP operations and product development
Manage project scheduling and ensure timely delivery of project goals
Lead design, fabrication, installation, and troubleshooting of systems
Develop P&ID's alongside Automation and Chemical Engineers
Document systems to comply with GMP requirements
Guide the use of CAD standards and templates
Supervise installation operations conducted by outside contractors
Interact with consultants and vendors on design modifications
Create documentation supporting GMP processes and quality control
Prepare standard operating procedures and reports
Mentor junior colleagues in technical aspects
Benefits
Collaborative work environment
Opportunities for professional development
Access to advanced CAD tools and technology
Exposure to cutting-edge pharmaceutical engineering practices
Potential for project-based learning and skills enhancement
Full Job Description
Job Description
Lonza Pharma & Biotech is seeking a Senior Mechanical Engineer for their Engineering, Maintenance, and Facilities team in Bend, OR.
As a Senior Mechanical Engineer, you'll be responsible for overseeing the design, installation, modification, support and repair of pharmaceutical process equipment and building systems. A successful candidate will demonstrate proficiency in mechanical design, familiarity with fabrication and machining, and possess a collaborative mindset; working with other colleagues on multiple projects in a fast-paced environment.
Responsibilities include but are not limited to the following:
Collaborate with engineers, designers, fabricators, and machinists to design in 3D pharmaceutical processing equipment
Collaborate with internal multi-disciplinary team members to design/modify equipment to support GMP operations, product development, and R&D activities.
Support scheduling and coordinate work plan execution to ensure safe, high-quality, and on-time delivery of project deliverables across multiple projects.
Serve as the lead or supporting engineer for design, fabrication, installation, and troubleshooting of equipment and facility systems across all groups.
Develop system P&ID's (Piping & Instrumentation Diagram) in collaboration with Automation and Chemical Engineers
Fully document systems and components to satisfy GMP requirements
Provide input on standards and templates for drawings (including title blocks, revision schemes, electrical diagrams, weld callouts)
Use a CAD Data Vault (SolidWorks PDM Professional) in day to day CAD system (SolidWorks) operation
Interface with and direct outside contractors, oversee equipment installation
Consult with other colleagues, consultants, or vendors on design and layouts
Generate GMP documentation supporting change control, qualification, CAPA, and deviation/investigationactivities.
Prepare written documents such as standard operating procedures, memos, reports, and standards.
Act as a technical and professional mentor for junior colleagues.
Physical demands:
Able to work in a GMP clean environment when needed to support manufacturing
Able to use stairs and regularly stand or sit for prolonged periods of time
May be required to push, pull, lift or move items weighing up to 50 pounds
Qualifications:
B.S. or M.S. in Mechanical Engineering or equivalent engineering education
Knowledge and use of SolidWorks or other 3D CAD, DraftSight/AutoCAD and MS Office required
Demonstrable strong mechanical, analytical and technical skills.
Experience mentoring and developing junior engineers is preferred
Extensive equipment/system engineering design
Knowledge of design for hygienic equipment (pharmaceutical, food/dairy, semiconductor, etc.) is a plus
Knowledge of and familiarity with GMP standards is preferred
Knowledge and use of SolidWorks PDM Professional preferred
Knowledge of P&ID's and drawing standards preferred
Experience in a manufacturing environment preferred
Experience with hand, power, and machine tools as well as welding, fabrication, and sheet metal is a plus
Able to work on multiple projects and meet project deadlines as needed
Demonstrate good oral and written skills
Qualifications
Additional Information
About Lonza America Inc
Lonza America Inc is a subsidiary of Lonza Group, a Swiss multinational company that provides products and services to the pharmaceutical, biotech, and specialty ingredients markets. Lonza America Inc is responsible for the North American market and offers a range of products and services, including custom manufacturing, research and development, and quality control testing. The company has a strong focus on sustainability and has implemented various initiatives to reduce its environmental impact. Lonza America Inc was founded in 1897 and has since grown to become a leading provider of products and services in the pharmaceutical and biotech industries.
