Job Description:
Responsibilities:
- Support the methods development and validation to test new products manufactured at the site.
- Perform analytical interpretation and analytical logistics from laboratory operations.
- Participate in the transfer of analytical technology to commercial laboratories (method transfer).
- Work with a minimum supervision and prepare summaries of experimental trials.
- Perform data interpretation results obtained during method transfer and / ormethod development.
- Keeps track of the reagents and supplies inventory in the PD Laboratory.
- Support the EHS program to assure compliance with safety policies.
Requirements:
- Education: Bachelor´s degree in Science on Chemistry or higher.
- Minimum two (2) years of direct related experience in laboratory method development,validation, cleaning methods validation protocols and analytical technologytransfer.
- Experience in a cGMP regulated analytical laboratory and previous participation in method development, validation and analytical technology transfer.
- Knowledge in FDA, USP and ICH guidelines for method development andvalidation is required.
- Computer literate.
- Bilingual (Spanish and English) – written and verbal.
Work Methodology:
- Full time on-site job
- 1st or 2nd work shift (subject to changes based on project needs)
- 3 months of initial contract