Principal Process Scientist
Manatí, PR, Puerto Rico
Contracted
Pharmaceutical
Experienced
For services as Principal Scientist.
WHAT MAKES YOU A FIT: .png)
The Technical Part:
- Bachelor’s degree in Pharma, Chemistry or Engineering & five (5) years of exposure in the Pharmaceutical industry.
- Experience in:
- Extensive experience providing operational, scientific, and compliance support for sterile manufacturing environments.
- Strong background in manufacturing investigations (QE's), CAPAs, deviation management, triages, and procedural development/revisions.
- Proven expertise in supporting equipment troubleshooting and providing technical guidance to manufacturing operations.
- Hands-on experience leading and supporting Technology Transfer projects, including project planning, team coordination, and new product introductions.
The Personality Part:
- Being self-motivated means that you are curious, 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 have a commitment to serving customers with high-quality research and products, to embracing a diverse work culture, and even to 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)
- Performs as Subject Matter Expert in liquid, lyophilized and syringe parenteral processes, and formulation, maintaining a current knowledge base on best industry practices.
- Supports Technical Transfer projects, including project plan development, team formation and charters for new product transfers.
- Develop and execute experimental, characterization and validation protocols.
- Partners with, Information Management, Engineering Maintenance, and Manufacturing to ensure equipment and automation are capable to deliver the manufacturing processes transferred.
- Assures effective integration of plans and resources to achieve timeliness of process support, productivity, and technology transfer and validation activities associated to product portfolio.
- Performs Design of Experiments and Process Risk Assessment (FMEA’) activities to establish appropriate process control strategies, perform equipment characterization exercises.
- Partners with the site management team in the identification of best practices in industry related to technology transfers, pharmaceutical technology to create a competitive advantage.
- Develops and maintains effective working relationships with other division groups in support of technology transfer, validation, productivity, and process support activities.
- Performs as the communication liaison for the transfer, validation, optimization, and daily support activities for the assigned product portfolio.
BEING A FITS PIECE COMES WITH PERKS:
- One of these is the excellent, unmatched, never-before-seen customer service of our team (trust us, you’ll be amazed). However, that’s not all we have to offer. Talk with us to find out!
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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