Process Engineer

Carolina, PR, Puerto Rico
Contracted
Pharmaceutical
Mid Level

For Process Engineer services in the Engineering / Manufacturing area. 

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor’s degree in engineering (preferred chemical or mechanical) and (3) three years experience in the pharmaceutical manufacturing industry. 
  • Bilingual: Spanish and English
  • Soft Skills: Organizational skills 
  • Shift: Administrative and according to business needs. 
  • Experience in:
    • Manage multiple project objectives or assignments.
    • Technical Writing. 
    • Process Equipment (Dry Product Operations.) 
    • DPO technologies/processes 
    • GMP & GDP regulations.

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 of 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 Be The Piece?

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

  • Provide DPO support as equipment/asset steward for the areas to maintain an efficient manufacturing process.
  • Establish and maintain technical information on the process and unit operations within the manufacturing process.
  • Develop and monitor process and capacity indicators to identify and address performance issues and identify improvement opportunities.
  • DPO technologies/processes include Wet Granulation; Roller Compaction; Tablet Compression/Coating/Inspection/Printing; and others. 
  • Perform troubleshooting and investigation on unexpected issues. Own equipment-related deviations, CAPAs, and changes.
  • Lead or participate in investigations, and problem-solving activities such as root cause analysis.
  • Provide technical expertise for requirements, design, selection, installation, qualification, operation, maintenance, and reliability of process equipment.
  • Perform and summarize improvement opportunities in technical reports, investigations, plant/lab trials, data analysis, and process modeling.
  • Maintain regulatory documentation.
  • Support qualification activities.
  • Ensure the process complies with current industry regulatory expectations, new regulations, and corporate policies and programs for Quality, Health, and Safety & Environmental, Process Safety.
  • Lead Machine Guarding and LOTO Assessments across the site.

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?

Share

Apply for this position

Required*
Apply with Indeed
We've received your resume. Click here to update it.
Attach resume as .pdf, .doc, .docx, .odt, .txt, or .rtf (limit 5MB) or Paste resume

Paste your resume here or Attach resume file

Human Check*