Arrowhead Pharmaceuticals→
Associate Engineer I, Process Engineering
Entry LevelOn-site
Location
Verona, WI
Salary
$60k–$70k/yr
Experience
Not specified
Posted
1 week ago
Skills
process engineeringmanufacturing environmentdata analysis toolsprocess safety assessmentshazop studiesequipment qualificationp&id reviewgmp environmentsafety regulationsprocess optimization methodologiesexperimental design
Job Description
Summary: Arrowhead Pharmaceuticals is a commercial stage biopharmaceutical company focused on developing innovative drugs for diseases with a genetic basis. As an Associate Engineer I in Process Engineering, you will contribute to enhancing manufacturing processes through safety improvements, technical support, and equipment management.
Responsibilities:
- Collaborate with cross-functional teams to translate experimental findings into actionable process improvements
- Perform experiments in collaboration with your supervisor to optimize existing processes or develop new ones
- Participate in process risk assessments and recommend mitigation strategies
- Participate in hazard and operability (HAZOP) studies and process safety assessments
- Collaborate with manufacturing and safety teams to identify safety improvements
- Maintain safety systems to ensure the process remains in a ready state and future safety issues can be prevented
- Demonstrate and support a culture of safety awareness and compliance within the production team
- Provide technical support for production operations, identify and assist resolution of manufacturing issues
- Support equipment and process qualification activities and ensure compliance with regulatory requirements
- Assist with troubleshooting and repair of equipment internally when feasible
- Manage spare part inventory
- Document repair and spare parts activities in BMRAM
- Manage lifecycle of equipment documentation for production equipment. This includes but is not limited to P&IDs, Design Documentation, Validation Documentation, and Equipment Qualification Records (EQRs)
- Review and update P&IDs for production processes, including equipment, instrumentation, and piping systems
- Follow P&ID change management processes, including version control and documentation updates
- Reference the design and validation documentation for equipment to ensure compliance and design intent are maintained
- Help develop batch records in a GMP environment
- Occasionally assist with production work as needed
Required Qualifications:
- Bachelor's degree in Chemical Engineering, or a related field
- 0-2 years of experience in process engineering or a similar role within a manufacturing environment
- Proficient in data analysis tools and software
- Excellent problem-solving skills and the ability to apply analytical thinking to identify and resolve process-related issues
- Strong communication and interpersonal skills, with the ability to collaborate effectively across cross-functional teams
- Good verbal and written communication skills
- Excellent technical writing skills with high attention to detail
- Able to occasionally lift 50 lbs. unassisted
- Able to work for extended periods of time in a chemical fume hood
- Able to stand on feet for extended periods of time
Preferred Qualifications:
- Experience through research or internship/co-op
- Experience working in a GMP setting with controlled documentation
- Knowledge of safety regulations, process optimization methodologies, and experimental design
Required Skills: Process engineering, Manufacturing environment, Data analysis tools, Process safety assessments, HAZOP studies, Equipment qualification, P&ID review, GMP environment, Safety regulations, Process optimization methodologies, Experimental design
Benefits: Competitive salaries, Excellent benefit package
Benefits
Competitive salaries
Excellent benefit package