MAIN PURPOSE OF ROLE
This position is responsible to provides quality support for the production process, provides support to Quality Engineering during nonconformance processes and other process or daily activities..
This position is responsible to bring support manufacturing lines following costumer service techniques.
**MAIN RESPONSIBILITIES**:
- Support manufacturing lines, with clarification of documental doubts and correction of documentation errors.
- Monitoring documentation the errors metric of the production line.
- Coordinates with Quality Engineer to prepare and handle the material in and out of the designated quarantine area.
- Reviews compliance of quality and manufacturing documentation such as batch records.
- Identifies and segregates nonconforming material from the production line according to governing documents.
- Provides support in the process related to nonconformance actions (corrective, preventive or corrections) rework or Short activities.
- Provides support in the process related Build as Risk (BAR's)
- Provides support in the investigation process related to Manufacturing Analysis (MA) as training evidence, material expiration.
- Assists to sets up and in the training for the new or transferred Quality Technicians
QUALIFICATIONS
Education
- Student of Engineering (at least 30% of degree completion) or Technical Degree (at least 50% of diploma completion), Engineering, quality or related fields
- Minimum 2 years of equivalent experience in medical devices or pharmaceutical quality control
- Basic use of MS Office software.
- Knowledge of Quality Systems/engineering, required.
Experience
- 0 years
Language Proficiency
- Basic English level / Required
Preferred Qualifications & Education
- Knowledge in blueprint reading and experience with sampling techniques.
- Prior medical device experience.
- Basic knowledge of statistical techniques/ tools.
**_ Shift TC_