Medical Device Manufacturing Engineer – Process Validation

Techtrueup; Indianapolis (IN); Sur place; USD 75 000 - 95 000; Plein temps

Résumé du poste

Techtrueup is seeking a Manufacturing Engineer in Indianapolis, IN, for a 6-month contract, focusing on supporting medical device manufacturing processes. The role involves developing validation strategies, ensuring compliance with FDA and ISO standards, and collaborating with cross-functional teams to implement effective solutions.

The ideal candidate will possess strong problem-solving skills, experience with process validations, and knowledge of quality control tools. This position offers an opportunity to contribute to innovative medical device projects.

Qualifications

• Experience supporting medical device manufacturing process validations.
• Knowledge of design control and cGMP requirements.
• Ability to lead and prioritize multiple project assignments.

Responsabilités

• Develops process validation strategies and creates plans.
• Ensures regulatory compliance per FDA and ISO standards.
• Collaborates across teams to implement solutions.

Connaissances

Process validations for medical devices

Test method validation

Root cause analysis

Quality tools

Cross-functional teamwork

Outils

Microsoft Office Suite

Statistical process control

Description du poste

Techtrueup is seeking a Manufacturing Engineer in Indianapolis, IN, for a 6-month contract, focusing on supporting medical device manufacturing processes. The role involves developing validation strategies, ensuring compliance with FDA and ISO standards, and collaborating with cross-functional teams to implement effective solutions.

The ideal candidate will possess strong problem-solving skills, experience with process validations, and knowledge of quality control tools. This position offers an opportunity to contribute to innovative medical device projects.