Process Engineer

Flexible & Integrated Technical ServicesAñasco, PR
13d

About The Position

For Engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s degree in Engineering and a minimum of three (3) years of exposure in Validation activities within the Pharmaceutical or Medical Device Industry. Excellent verbal/written communication skills (English and Spanish) Shift: Administrative & according to business needs 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) 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?

Requirements

  • Bachelor’s degree in Engineering and a minimum of three (3) years of exposure in Validation activities within the Pharmaceutical or Medical Device Industry.
  • Excellent verbal/written communication skills (English and Spanish)
  • Experience in Validation Management & Process Improvement
  • Leading projects, managing timelines, and effectively communicating with stakeholders.
  • GMP & GDP regulations

Responsibilities

  • Lead and execute validation activities for process changes and equipment modifications.
  • Manage validation projects ensuring compliance with regulatory standards and company policies.
  • Drive improvements in existing tooling and redesign workstations to enhance process robustness.
  • Develop and implement process control strategies for manufacturing operations.
  • Prepare and maintain validation documentation, protocols, and reports.
  • Coordinate cross-functional teams to ensure timely completion of validation tasks.
  • Provide training to personnel on validation procedures and document updates.
  • Monitor and report project progress to key stakeholders regularly.
  • Identify opportunities for continuous improvement in validation and process control.
  • Ensure adherence to safety, quality, and regulatory requirements throughout all activities.
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