JT472 - PROCESS ENGINEER I

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies, manufacturing techniques as well as production yields for existing or new products.
• Integrates equipment and material capabilities to meet process module target specifications and technology target specifications.
• Reviews product development requirements for compatibility with processing methods to determine costs and schedules.
• Interacts with product design and development personnel to ensure that processes and designs are compatible.
• May develop and conduct statistical analysis or recommend additions to document work.
• Leads the innovation, development and/or optimization of new manufacturing concepts, processes and procedures for transfer to manufacturing operations.
• Develop, execute, and close protocols required as part of the validation lifecycle.
• Supports equipment installation and assessment of inputs, outputs and alignment to requirements.
• Ensures processes and procedures are in compliance with regulations.
• Develops manufacturing processes that are applicable to statistical process control and may develop those techniques including the measurement systems. 

Qualifications:

• Bachelor’s degree in engineering
• 2 years of relevant experience
• Investigation and root cause analysis skills
• Technical writing knowledge
• Process Validation and Computer software validation knowledge
• 1st Level Troubleshooting Skills
• Equipment Validation
• Fully Bilingual
• Troubleshooting skills
• Availability for 1rst shift