Title: Eng, Automation
Walker, MI, US
At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
This is an onsite position requiring the team member to be onsite 5 days a week. No relocation is provided for this opportunity.
Job Summary
In this role, you will be responsible for maintaining operation efficiency of automated assembly lines. Provide support to shift operations as needed. Develop long-term predictive/preventative maintenance plans for all assembly equipment.
Essential Duties and Responsibilities
- Assist in the design, programming, and integration of automation solutions for production lines, including robotics, PLCs, HMIs, and vision systems.
- Support continuous improvement initiatives to optimize manufacturing processes, increase efficiency, and reduce downtime.
- Collaborate with senior engineers to document, test, validate, and implement process control changes according to company and regulatory (FDA, ISO 13485) standards.
- Aid in the maintenance and troubleshooting of automated equipment to ensure reliable operation and minimal disruption to production.
- Participate in equipment qualification (IQ/OQ/PQ) and the development of related documentation.
- Collect and analyze production data to identify improvement opportunities and support root cause analysis of automation-related failures.
- Work closely with cross-functional teams (Engineering, Quality Assurance, Maintenance, and Production) to support daily manufacturing operations.
- Maintain up-to-date records of modifications, configurations, and maintenance activities in compliance with Good Manufacturing Practice (GMP) guidelines.
- Evaluate, install, and maintain machine guarding systems and safety interlocks to ensure that automated equipment operates in compliance with OSHA, ISO, and internal safety requirements.
- Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
- Performs other duties as assigned by management.
- Exhibits regular, reliable, punctual and predictable attendance.
Automation includes – assembly machines/fixtures, label applicators, robots, end of arms, separators and test equipment. Any other equipment assigned by management.
Education
- Education or Equivalent Experience: 4-year technical degree.
Preferred Knowledge, Skills and Abilities
- 0 - 3 years of experience in related industry.
- Experience in medical device industry or other regulated industry.
- Background with medical/pharmaceutical clinical trials would be a plus.
- Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and ISO 9002.
Travel Requirements
Physical Requirements
West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening.
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