At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https: //www.jnj.com

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About MedTech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at https: //www.jnj.com/medtech

We are searching for the best talent for Senior Metrology Engineer to be in Grecia, Costa Rica.

Purpose:

The Senior Metrology Quality Engineer will be responsible for leading the definition of inspection requirements and qualification of inspection and test methods used in the manufacturing of orthopeadic implants and instruments.

You will be responsible for:

Under the direction of the Senior Quality Engineering Leader, and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Interprets drawings featuring Geometric Dimensioning & Tolerancing (GD& T) per ASME Y14.5 to identify product inspection requirements.
• Identify product inspection requirements.
• Serves as technical expert for metrology inspection.
• Facilitates, encourage and coordinate continuous improvement with respect to inspection activities.
• Coordinate data collection parameters for inspection measurements where required.
• Provides guidance on installation of inspection assets as to ensure compliance to procedures.
• Develops inspection strategies to meet business needs.
• Development of standard platforms where applicable (vision systems, contact/noncontact inspection systems.
• Develop method of “gauge” evaluation to consider, calibration frequencies, gauge life, fit for purpose, etc.
• Lead on development of inspection fixturing to ensure minimum measurement error during inspection.
• Participates in reviews on cross-functional teams to ensure that conformance to specifications, inspect ability, reliability, and quality system objectives are met.
• Assist engineers with qualification and validation of new or changed tooling or parts.
• Work from written or verbal instructions, detailed engineering drawings, and 3D models.
• Writing of work instructions for qualification of inspection techniques relating to standard platforms.
• Input into validation approach in conjunction for all inspection platforms.

Qualifications / Requirements:

• A minimum of a high school diploma. Bachelor’s Degree in engineering: Mechanical, Electrical, Industrial or applicable science is preferred.
• 4 years experience as a Quality Professional in the Medical Device Industry required.
• Demonstrated knowledge of manufacturing and inspection principles and practices, and procedures

Skills:

• Experience in selection and procurement of inspection equipment
• Proficient in writing and editing CMM programs (PC-DMIS/COSMO/CALYPSO)
• Proficient in set-up and operation of inspection equipment
• Proficient in metrology methods/technology
• Proficient in reading/interpreting engineering drawings and the application of Geometric Dimensioning & Tolerancing (GD& T) per ASME Y14.5
• Proficient in mathematical applications - Algebra, Geometry, & Trigonometry
• Proficient in Microsoft Word & Excel.
• Excellent interpersonal & communication skills
• Knowledge of mechanical inspection methods and tools used to determine product acceptance
• Ability to investigate and learn new technologies in metrology

Preferred:

• Minimum 3 years in CMM programming PC-DMIS / COSMOS / CALYPSO programming experience
• Experience with laser scanning techniques and other inspection technologies.
• Familiarity with statistical analysis software (i.e. Minitab)
• Knowledge of 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry
• Working knowledge of GMP and Quality Systems (FDA/ISO) within a regulated environment.
• Certifications such as CQA, CQE, CQM (preferably), CBA, MBB or BB are a plus