Associate Manufacturing Engineer- 01

Barceloneta, PR, Puerto Rico
Contracted
Pharmaceutical
Mid Level

For engineering services in the manufacturing area. 
WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor’s Degree in Engineering and two (2) years of experience in the Pharmaceutical or Medical Device industry.
  • Bilingual (English & Spanish). 
  • Project Management skills. 
  • Shift: 1st and according to business needs. 
    • 5:00 AM to 2:00 PM
  • Experience in:
    • Application and principles of Manufacturing/Process
      Engineering.
    • Effectively communicate cross-functionally to assist with resolving
      Quality/Engineering issues.
    • Office applications: Word, PowerPoint, Excel.
    • Statistics.

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)

  • Responsible for product/process knowledge and understanding of basic cause and effect of line and process changes.
  • Responsible for providing the line with related Engineering fixes, such as tooling (TLTs) and Manufacturing Aids( from idea definition to implementation).
  • Support maintenance technicians and supervisors in equipment availability issues.
  • Review equipment work order completion and performs product impact analysis in order to release equipment for commercial manufacturing use.
  • Supports Training and Certification Program.
  • Responsible for determining quality impact of Out-of-Tolerance documents.
  • Responsible for execution of line related change management (material, equipment and process changes).
  • Responsible for CO and simple CR generation related to changes impacting the manufacturing line.
  • Responsible for simple continuous improvement projects development and execution.
  • Responsible for exception subtask execution.
  • Evaluates ideas from the LPI program for potential implementation.
  • Leads root cause analysis efforts for basic/simple manufacturing events, utilizing DMAIC model and A3s. Supports CAPA (Major) investigations with data gathering and analysis as needed.
  • Runs studies and validations on the line as needed. Writes protocols and reports with oversight.
  • Line support representative for related projects such as yield improvements, CIP's, productivity, quality and safety.

WHO WE ARE:

We are a Service Provider company different from the rest. We pride ourselves in 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 our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! 

Are you the Next Piece?

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