What are the responsibilities and job description for the Manufacturing Technician position at Glaukos Corporation?
Manufacturing Technician I – Burlington, MA
GLAUKOS #DareToDomore
How will you make an impact?
The Manufacturing Technician I will perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality management system (QMS) medical device good manufacturing practices (GMP) requirements.
What will you do?
- Maintain proper cleanroom environment (including gowning, room cleaning, and supplies)
- Follow, execute, and adhere to documentation in accordance with cGMP, QMS, and GDP requirements: protocols, specifications, work instructions (WIs), standard operating procedures (SOPs), batch records (BRs), device history records (DHRs), and engineering batches.
- Perform basic calculation and data entry
- Ability to assemble, disassemble, and clean process equipment
- Ability to clean, etch, passivate, assemble, and inspect components
- Process and assemble components in accordance with documented specifications and procedures
- Prepare bulk drug formulation operations
- Perform filling, capping and crimping operations
- Perform packaging and labeling operations
- Perform in-process inspection of assemblies and finished products in accordance with specification criteria
- Organize and clean the work areas
- Ability to perform validation and qualification activities (IQ/OQ/PQ/PV)
How will you get here?
- To be successful in this role, you will need to have the following industry (medical device, pharmaceutical, and/or biotechnology) and educational experience.
- It is highly desirable to have experience working in and maintaining a clean room in accordance with GDP, cGMPs, and QSR standards.
- 0 – 3 years’ experience with high school diploma.
#GKOSUS
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