C&Q Executer
Flexible & Integrated Technical Services, LLC · fitspr.com
United StatesOn-siteEntry level2+ yrsContract
The job in short
Commissioning and qualification (C&Q) execution for pharmaceutical equipment and validation protocols.
Details
- Found
- 21 d ago · posted 2026-09-17
- Location as listed
- Juncos
- Role
- Engineer (other)
- Source
- The company’s own careers site
Full description
For C&Q services in the Business Operations area.
WHAT MAKES YOU A FIT:
The Technical Part:
• Bachelor’s Degree in Science, or Engineering field with at least 2 years of proven experience in commissioning and qualification processes, protocol generation and execution.
• Bilingual (Spanish and English.)
• Shift: Administrative and according to business needs.
• Experience in:
• Executing commissioning and qualification activities in the field.
• Generating protocols and technical documents in line with current industry standards and regulatory requirements (e.g., cGMP, FDA, ISPE/ASTM E2500).
• Reporting deviations during tests, proposing corrective actions, and participating in the implementation and verification of corrections.
• Planning and coordinating resources, measurement/calibration equipment, and tooling needed for tests.
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 the planning and execution of commissioning, qualification, and validation (CQV) activities.
• Develop qualification protocols
• Support and influence effectively to ensure all necessary Commissioning, Qualification, and Validation (CQV) activities are completed on time and according to the validation program.
• Developing validation status reports.
• Participate in and support Factory Acceptance Test (FAT) and Site Acceptance Test (SAT) of new equipment.
• Record results legibly and verifiably, following data integrity principles (ALCOA) where applicable.
• Report deviations during tests, propose corrective actions, and participate in the implementation and verification of corrections.
• Plan and coordinate resources, measurement/calibration equipment, and tooling needed for tests.
• Comply with site safety rules, permits, and policies while on 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?
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