Principal Process Scientist

For services as Principal Scientist.

WHAT MAKES YOU A FIT:

The Technical Part:

• Bachelors degree inPharma Chemistry or Engineering & five (5) years of exposure in the Pharmaceutical industry.
• Shift: Administrative and according to business needs.
• Billingual (Spanish & English)
• Experience in:
  • Extensive experience providing operational scientific and compliance support for sterile manufacturing environments.
  • Strong background in manufacturing investigations (QEs) 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 youre 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 were 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 processesand 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 withInformation Management Engineering Maintenance and Manufacturing to ensure equipment and automation are capable ofdeliveringthe manufacturing processes transferred.
• Ensureseffective integration of plans and resources to achieve timelyprocess support productivity and technology transfer and validation activities associated with theproduct portfolio.
• Performs Design of Experiments and Process Risk Assessment (FMEA) activities to establish appropriate process control strategiesandperform equipment characterization exercises.
• Partners with the site management team toidentifyindustrybest practices intechnology transfersandpharmaceutical technologyto 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 youll be amazed). However thats not all we have to offer. Talk with us to find out!

WHO WE ARE:

We are a Service Provider companydifferent from the rest. We pride ourselves in how we treat the most important piece of our companys 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 industryclients with top-notch quality talent.Were FITS!

Are you the Next Piece