Specialist Manufacturing

 For Manufacturing services in the Inspection and Vials Packaging area.

WHAT MAKES YOU A FIT: 

The Technical Part:

• Bachelor’s Degree (preferable in Engineering or Life Sciences) with five (5) years of direct experience as a Quality Professional in the regulated industry.
• Bilingual (English & Spanish)
• Project Management skills
• Shift: Administrative and according to business needs. 
• Experience in:
  • Change control, CAPA, VAPA EV, Deviations and Documentation. 
  • Support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. 
  • Compliance, Analytical and Troubleshooting to support manufacturing operations. 

The Personality Part:     

• Being self-motivated means that you are curious and anxious to explore all possibilities without anyone telling you to (while also following instructions, of course). It means you’re creative, with such an eye for detail, that nothing gets past you. If this sounds like you, and if you commit to serving customers with high-quality research and products, embracing a diverse work culture, and even the environment, you might just be what we’re looking for!

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

• Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
• Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.
• Provide troubleshooting support.
• Assist in generation of training materials and may assist in providing training on scientific or technical aspects of the process.
• Support establishment of process monitoring parameters and control limits. Collect process-monitoring data and support the assessment of deviations.
•  Provide support of timely execution of the process monitoring quarterly reports.
• Ensure that all Non-conformances are triaged within the established goal.
• Responsible for authoring investigation reports. Responsible for execution of corrective actions.
• Assist with generation of process validation protocols and reports.

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?