Welcome to Beckman Coulter, a global leader in the biomedical industry dedicated to advancing scientific research and improving patient outcomes. We are seeking a skilled and motivated individual to join our team as a Process Engineer II. In this role, you will play a vital part in optimizing our manufacturing processes and ensuring the highest quality standards for our products. As a Process Engineer II, you will have the opportunity to work alongside a talented and diverse team, utilizing your strong technical skills and problem-solving abilities to drive continuous improvement. The ideal candidate will have a degree in engineering or a related field, along with a minimum of 3 years of experience in process engineering within a regulated industry. If you are passionate about making a positive impact in the healthcare field and possess a strong attention to detail and a drive for excellence, we invite you to apply for this exciting opportunity.
Conduct research and analysis to identify areas for process improvement within the manufacturing department.
Utilize technical knowledge and problem-solving skills to develop and implement solutions for process optimization.
Collaborate with cross-functional teams to ensure seamless integration of new processes and procedures.
Monitor and analyze manufacturing data to identify trends and make data-driven decisions.
Develop and maintain process documentation, including standard operating procedures and work instructions.
Lead and participate in root cause analysis and corrective action processes to address any quality issues in the manufacturing process.
Act as a subject matter expert for process-related inquiries and provide technical support to production teams.
Identify and implement cost-saving measures while maintaining quality standards.
Stay updated with industry trends and advancements to continuously improve processes and techniques.
Train and mentor junior engineers and technicians in process improvement methodologies and techniques.
Ensure compliance with all regulatory requirements and company policies.
Collaborate with suppliers and vendors to evaluate and qualify new equipment and materials for use in the manufacturing process.
Participate in cross-functional projects and initiatives to drive continuous improvement and overall business success.
Communicate effectively with team members and management, providing regular updates on process improvement initiatives and results.
Where is this job?
This job is located at West Sacramento, CA, USA
Job Qualifications
Bachelor’s Or Master’s Degree In Chemical Engineering, Mechanical Engineering, Or A Related Field.
Minimum Of 3-5 Years Of Experience In A Process Engineering Role, Preferably In The Medical Device Industry.
Strong Knowledge Of And Experience With Process Design, Validation, And Optimization.
Proficiency In Computer-Aided Design (Cad) Software, Statistical Analysis Tools, And Process Simulation Software.
Excellent Communication And Interpersonal Skills, With The Ability To Effectively Collaborate With Cross-Functional Teams And Present Technical Information To Non-Technical Stakeholders.
Required Skills
Quality Assurance
Project Management
Data Analysis
Lean Manufacturing
Statistical Analysis
Technical Writing
Root Cause Analysis
Continuous Improvement
Process Validation
Risk Assessment
Process Optimization
Problem
Soft Skills
Communication
Conflict Resolution
Leadership
Time Management
Creativity
Critical Thinking
Teamwork
Adaptability
Problem-Solving
Empathy
