Quality Engineer - Process Development

 For Quality Engineering services in the Process Development area. 

WHAT MAKES YOU A FIT: 

The Technical Part:

• Bachelor’s Degree in Engineering and 5 years of experience in the review and approval of life cycle validation documentation in the regulated industry. 
• Bilingual: Spanish and English
• Soft Skills: Attention to detail, organization, and writing skills
• Shift: Administrative, and according to the business
• Experience:
  • Process and/or equipment validation activities (IQ, Characterization, OQ/ PQ).
  • Develop Master validation plans for new processes or products.

The Personality Part:    

• Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients, and team members. In other words, being a customer service pro is one your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to take on this new challenge?
   

AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)

• Support process and/or equipment validation activities (IQ, Characterization, OQ/ PQ); process performance qualification activities and develop Master validation plans for new processes or products.
• Responsible for reviewing process validation protocols and reports. Support other functional areas during the validation activities.
• Collaborate with the Process Development team to efficiently qualify new processes; assist on statistical sampling plans, and other development procedures.
• Design and develop in-process and receiving quality systems for new processes and components.
• Define gages, tools and equipment for the test methods developed.
• Identifies and controls Manufacturing process defects (scrap, nonconforming material, customer complaints) by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying & bounding data to support implementation of complex & documenting release criteria.
• May be responsible for creating risk analyses and FMEAs.
• Develops Process Monitoring Systems by identifying critical process steps applying methods to reduce process variation to reduce/eliminate the cause of defects.
• Leads process improvement efforts by identifying methods to capture quality metric data and by performing appropriate analysis methods to enhance sustaining product design and new product development.
• Assists in creation of Quality Tools & Training Materials by understanding the limitations of existing quality tools and training materials, and by helping to identify more effective tools & materials.
•  Evaluates the adequacy and compliance of systems, operations, and practices against regulation and company documentation. Could serve as auditor of areas of the clients' quality system, such as development and manufacturing, as assigned.

We are a Service Provider company different from the rest. We pride ourselves on how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities, and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented, and focused on the well-being of our resources, while providing our Pharmaceutical, medical device, and Manufacturing industry clients with top-notch quality talent. We're FITS! 

Are you the next piece?