Support environmental control activities, executing environmental routine testing for viable and non-viable particles for air and product contact surfaces follow quality system and in compliance with Good manufacturing practices.
Responsibilities
Perform investigation process for out of tolerance equipment
Include new equipment at the calibration and maintenance system
Review and approve cleanroom intrusion plans
Get involved in various stages of equipment and processes validations: run or write protocols and reports for IQ, OQ, PQ and TMV; as well as any other document relating to validation
Performs or coordinate microbiology testing as offered by the Microbiology Lab, including LAL, Bioburden, Environmental monitoring
Requirements
Microbiology or Quality Technician
Biotechnology, Microbiology and Biology Bachelor degree
Lead end-to-end design release of Overhead Systems components for automotive client programs, managing technical data, supplier engagement, DFMEA, DVP&R, tooling milestones, and cross-functional coordination.
Responsibilities
Lead end-to-end design release of Overhead Systems components
Own and manage all technical data across Client systems
Drive supplier engagement through all APQP gates
Build, own, and actively manage DVP&R plans
Support prototype builds and attend in-plant build events
Requirements
Bachelor’s degree in Mechanical Engineering, Automotive Engineering, or related field
Nice to have: International Tier 1 and OEM experience
Nice to have: In-plant experience with tool tryouts, prototype builds, assembly line support
Nice to have: Familiarity with Client-specific processes and milestones
Nice to have: Experience in the full sourcing process
Partner with CSP’s leaders and staff to establish and maintain a culture of quality in line with business strategy
Direct quality assurance operations for CSP to establish clear policies, processes and metrics in line with business strategy and regulatory requirements
Optimize and maintain CSP’s Quality Management System
Lead process improvements for greater efficiency, speed of delivery, and cost savings by implementing new quality procedures and processes tailored to the uniqueness of CSP’s products and services
Establish quality practices that are clear and efficient, enabling scalability of the business whilst always ensuring customer satisfaction is maintained
Supports the manufacture of aerospace transparency components by ensuring materials, processes, and finished assemblies meet engineering drawings, customer requirements, and AS9100 quality standards.
Compensation
Payrate: $24.18 / hour
Responsibilities
Perform in‑process, final, and receiving inspections of aerospace transparency components and assemblies
Inspect to engineering drawings, specifications, and quality requirements
Verify compliance with AS9100, customer, and regulatory standards
Perform and document First Article Inspections (FAI) per AS9102
Conduct dimensional and visual inspections using precision measurement tools
Requirements
High School Diploma or GED required
Technical certification, associate degree, or aerospace quality training preferred
Nice to have: Experience with aircraft transparencies, composites, structures, or assemblies
Nice to have: Experience using CMM or advanced measurement systems
Nice to have: Familiarity with customer or regulatory audits
Senior R&D Engineer – CAPA Specialist responsible for leading complex CAPA investigations within the Research & Development organization.
Compensation
Salary range: $115k - $140k; 10% STIP
Responsibilities
Lead and execute product design and or Design Controls process related CAPA investigations within the R&D organization, from problem definition through implementation and effectiveness verification.
Perform thorough and structured root cause analyses for design, verification, validation, and product performance issues using appropriate analytical tools and data.
Develop and drive robust corrective and preventive actions that are risk-based, technically sound, and aligned with design controls and risk management processes.
Ensure CAPA documentation is accurate, complete, and compliant with FDA regulations, ISO 13485, and internal quality system requirements.
Collaborate closely with cross-functional partners—including Quality, Regulatory Affairs, Operations, and Manufacturing Engineering—to address systemic and cross-functional issues.
Requirements
Bachelor's degree in Engineering or related technical discipline; advanced degree preferred.
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