When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.
Supports the organization with initial compliance and ongoing preparation, testing and monitoring of conformance to established quality assurance processes and standards for manufacturing and production. Performs evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards. Identifies risk and evaluates deficiencies while working with internal departments/business units to appropriately remedy them.
- Perform inspections of purchased parts, electro – mechanical subassemblies or finished company products according to pre- defined criteria using standard physical, mechanical and/ or electrical measurements.
- Rework or reject subassemblies or finished products as required.
- Evaluate problems and make initial recommendations for possible corrective actions.
- Be able to implement sampling plans using AQL table
- Basic knowledge of statistical applications
- Utilize required tools to conduct inspections (gauges and testing equipment)
- Initiate Non-Conformance reports as required
- Work with production management and Quality Assurance to provide feedback to assemblers regarding accuracy of assembly procedures.
- Perform review of Device History Records and other documentation for compliance to established procedures and Good Documentation Practices
- Maintain and audit Dock to Stock program for incoming materials.
- Maintain document files, test records and sample inventory in a timely and accurate manner.
- Assist in the writing and updating inspection procedures, protocol and checklists.
- Performed analysis and identified trends in the inspection of finished products, in-process materials and bulk raw materials, and recommended corrective actions when necessary
- Participates in Material Review Board meetings and product dispositions.
- Comply with all quality, safety, and work rules and regulations
- Coordinates the calibration process to ensure schedule service or repairs occur on time for equipment, fixtures and instrumentation.
- Escalates gaps in the schedule or compliance, maintains the calibration database and files.
- Resolve out of calibration equipment to determine risk to finished product
- Participate in continuous improvement team (Practical Process Improvement) activities and projects as required.
- Demonstrated documentation/ communication/ computer skills
- Self-starter, Team Player, Detail Oriented
- High ethical standards – will not compromise quality requirements
- Ability to escalate issues as needed
- Responsible and Accountable
- Ability to effectively communicate across multiple levels of the organization
- Proficient in Microsoft Office applications
- Agile PLM system experience preferred
- Intuitive ERP system experience preferred
- Root cause analysis training preferred
- CMM experience preferred
- High School Diploma or equivalent
- Experience in a Manufacturing Environment
Apply today! http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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