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.
- Application and principles of Manufacturing/Process
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?
Apply for this position
Required*