The Senior Equipment Supervisor will support large, complex engineering assignments, validations of equipment, and perform investigations for quality issues on the assigned Value Stream. The Senior Equipment Supervisor will manage complex engineering projects and will often manage a cross-functional project team.
Essential Functions & Accountabilities:
Executes engineering assignments independently such as ECNs, NPEs, LCNs, etc
Executes product transfers and acquisitions, managing the project throughout the PTR/PAR process
Executes product integrations from R&D
Execute validations of complex equipment and manufacturing lines
Owns specific equipment to perform Corrective and Preventative Maintenance and is responsible for investigations of EIRs/MIRs
Partners with the assigned Value Stream Team to ensure performance needs are met or exceeded by ensure enough capacity, minimum scrap variances, and labor efficiency when equipment are involved
Ensures that manufacturing validations, processes, and procedures comply with FDA, OSHA, ISO, and corporate regulations, policies and procedures.
Responsible for technical and equipment engineers’ development, including coaching, training and performance appraisal. Assists with hiring and onboarding process.
Manages all employee relations issues with Human Resources and Management to ensure company policies are being followed.
Guide equipment technicians and engineers to troubleshoot equipment malfunctions
Promotes a positive work environment in alignment with CooperSurgical mission, vision and values. Applies disciplinary actions as needed.
Define and execute improvement programs such as cost, quality, or capacity
Work with technical operations to modify part designs to improve manufacturability
Maintain a continuous improvement mindset and work with management to obtain buy in for technical improvement programs
Perform other duties as directed by management
Qualifications
Knowledge, Skills and Abilities:
In depth knowledge of project management, PMP preferred
In-depth understanding of equipment, equipment qualification and process validation.
Creative individual who is able to communicate and coordinate good ideas through to implementation. Ability to communicate well, both orally and written
Six Sigma Green Belt (Black Belt preferred) & solid understanding of Lean Principles.
Familiarity with programs such as Excel, SolidWorks, MiniTab, Microsoft Word, Power Point, etc.
Thorough understanding of medical device manufacturing, especially as it relates to FDA (GMP) manufacturing requirements
Fluent in Spanish. Ability to communicate well in English, both orally and written.
Contact with machinery
Work Environment:
Experience:
5-10 years of technical experience in manufacturing environment that is both labor and machine intensive.
At least 4-5 years of supervisory or managerial experience.
Experience with lab and chemistry equipment such as weighing scales, mixing processes and steam sterilizers is an advantage.
Education: