What are the responsibilities and job description for the Engineer II - Quality position at Rockline Industries, people who make it right?
Essential Accountabilities
Grade 11
- Facilitate and maintain validation project documentation, including site’s Validation Master Plan.
- Write Protocol.
- Execute Installation, Operation and Performance Qualification.
- Write final report for each qualification.
- Attend formal training on related software and/or equipment.
- Work closely with customer in development of validation requirements and protocols. Maintain validation protocol
- Serve as the Database administrator for Infinity QS (Statistical Process Control) software.
- Developing project databases to support Quality inline checks and manufacturing.
- Add associates to the database and assign login and passwords.
- Add process(s) and part(s) as necessary to support manufacturing.
- Update specifications to critical quality measures supporting our customer requirements.
- Troubleshoot application errors, assign root cause, determine solution and implement solution.
- Maintain input testing equipment for critical quality measurements.
- Provide Training on Statistical Process Control
- Provide statistical analysis support for manufacturing, new product development (NPD), trials, and validation activities.
- Develop SOP’s relating to validation and risk management.
- Monitor and prepare Key Performance Indicators (KPI’s) for major customers.
- Conduct quality/engineering studies to support manufacturing operations.
- Facilitate Corrective Action / Preventative Action (CAPA) activities to identify and resolve root cause issues through sound investigation and effective problem-solving techniques to solve problems within the manufacturing plant.
- Facilitate KT sessions for CAPA Projects.
- Execute the Effectiveness Check.
- Provide Training on the CAPA process
- Facilitate and train associates on quality topics required for their position (SPC / CAPA).
- Coordinate continuous improvement initiatives alongside internal and external (customer or supplier) representatives.
- Demonstrate commitment to Rockline/Iatric’s RRITE Values of Renew, Respect, Integrity, Teamwork, and Excellence.
- Associates have a direct and important role in ensuring that all work is performed in a safe manner. Effectiveness in carrying out this responsibility is part of each associate’s essential accountabilities.
- Contribute to a cooperative working effort by demonstrating a willingness to perform other job-related work, as needed or requested.
- Bachelor’s degree in Engineering, science or related field is required plus three or more years of engineering experience, preferably in a manufacturing environment.
- Technical background in nutritional products, laboratory diagnostics, medical devices, pharmaceutical, or similar industry. Experience in an FDA-regulated environment preferred
- Demonstrated ability to perform technical Non-Conformance investigations and Root Cause Analysis.
- Ability to work independently as well as collaboratively in a team setting with peers and colleagues in a cross functional setting.
- Able to prioritize and handle multiple tasks and ability to meet deadlines in a fast-paced work environment.
- Ability to have a flexible work schedule to support department activities and coordinate with production and validation execution schedules.
- Must be able to communicate face-to-face and over the phone
- Occasional lifting up to 35 lbs.
- Frequent standing/walking. Occasional sitting, bending, twisting, kneeling, climbing, pushing/pulling and reaching.
- Repetitive hand and foot movement.
- Work environment includes occasional noise, hot and cold temperatures.
- Requires ability to read, write, calculate and analyze.
Grade 11