For Medication Management services in the Pharmaceutical Industry. WHAT MAKES YOU A FIT: The Technical Part: Doctor of Pharmacy (Pharm.D.)
degree from an accredited pharmacy school and at least five (5) years of experience within the Pharmaceutical regulated industry. Valid and active pharmacy license in Puerto Rico. Detail-oriented with excellent organizational and time management skills.
Commitment to continuous learning and professional development.
Shift: Administrative according to the business need.
Bilingual: (English/ Spanish) communication skills, both written and verbal.
Experience in: Conduct process development, process validation and or cleaning validation.
Process improvement and optimization. Provide technical support for the introduction of new products, product transfer, technology and/or processes.
Support manufacturing operations. 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 of 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 Be The Piece?
AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Coordinates projects activities assigned. Review documents generated by the work group as delegated by Manager. Review accuracy of master formulas and approve as required. Represent Technology Services team in company / project group as delegated.
As required, represent Technology Services at Internation workshop related to new products, technology transfer, process/cleaning validation etc. Authorized designee for review and approval of Bill of Materials related to products manufactured.
In the absence of the Technology Services Manager, authorized designee to approve master production documents.
Periodically reviews strategy for the implementation of assigned projects.
Serve as project leader for special projects beneficial to the business needs.
Design technically sound experiments to identify and work with varibles that could possibly affect Develop,execute and report clearly defined programs to provide documented evidence of validated processes, cleaning procedures and/or equipment. Participate in manufacture of experimental, validation,stability and /ofr clinical batches if that is the role assigned. Oversees the cleaning experimental and validation activities as well as annual monitoring if that is the role assigned. 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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