Company Description
NovintiX is a leading provider of innovative engineering services, dedicated to transforming lives and shaping the future across diverse industries such as Medical Devices, Life Sciences & Healthcare, Aerospace & Defense, Automotive, Consumer Electronics, and Industrial & Heavy Equipment.
Guided by a mission to empower innovative solutions, NovintiX delivers best-in-class services to not only its clients but also its talented workforce.
With expertise in Product Engineering, Manufacturing, Quality Compliance, Clinical Affairs, and Digital Solutions, NovintiX is committed to excellence and technological advancements.
The company fosters an environment of growth, innovation, and continuous learning, positioning itself as a trusted partner and visionary in creating transformative solutions for its clients.
Role Summary:
We are seeking an experienced
CMM Programmer
to join our Metrology team supporting high-precision measurement and inspection processes within a regulated
Medical Device (MedTech)
environment.
The successful candidate will be responsible for developing, validating, and optimizing
CMM inspection programs using ZEISS Calypso software
, ensuring the highest standards of product quality and compliance with industry regulations.
Key Responsibilities:
Develop, optimize, and validate
CMM programs using ZEISS Calypso
to support product and process validation, new product introductions (NPI), and routine inspection.
Interpret
2D/3D CAD models, GD&T
, and engineering drawings to create robust measurement routines.
Conduct detailed
first article inspections (FAI)
and generate comprehensive inspection reports.
Collaborate with Design, Manufacturing, and Quality Engineering teams to ensure inspection processes meet product and regulatory requirements.
Maintain and calibrate metrology equipment, including CMMs and associated fixtures.
Support
MSA (Measurement System Analysis)
and
Gage R&R
activities.
Troubleshoot and resolve measurement or programming issues efficiently.
Document and maintain all inspection and validation records in compliance with
GMP
and
ISO *****
standards.
Support continuous improvement initiatives, ensuring alignment with Lean and Six Sigma methodologies.
Qualifications and Experience:
Bachelor's degree or diploma
in Mechanical / Manufacturing / Industrial Engineering or related field.
Minimum 5 years' experience
in a
MedTech or regulated manufacturing environment
.
Proven expertise in ZEISS Calypso programming
(advanced level preferred).
Strong understanding of
GD&T
and dimensional metrology principles.
Experience with
CMM validation
, equipment qualification, and inspection process documentation.
Working knowledge of
MSA, SPC, and CAPA
processes.
Excellent analytical, problem-solving, and communication skills.
High attention to detail, with a commitment to quality and compliance.
Preferred Skills (Nice to Have):
Experience with other metrology tools (e.g., Vision systems, Optical CMMs).
Knowledge of
ISO *****
calibration standards.
Familiarity with
Windchill PLM
or similar document control systems.
Exposure to
FDA, EU MDR
, and regulatory audit environments.