Description
The future service provider will perform physicochemical analyses for validation and development, completing the relevant documentation.
**Responsibilities**
* Complete documentation in accordance with GLP standards
* Perform all types of physicochemical tests for quality control and validation
* Enter obtained results into the Control System
* Enter obtained results into calculation spreadsheets, where applicable
* Deliver complete documentation to Quality Assurance
* Return samples to the Sample Management Department
* Correctly complete custody chains for test substances and reference substances
Requirements:
* Education: Completed undergraduate degree in Chemistry, Chemical Engineering, Chemical Processes, or Pharmacy.
* Experience in analytical method validation according to RDC 166; experience with RDC 964 is desirable.
* Extensive experience with analytical techniques such as liquid chromatography (HPLC), UV/VIS spectrophotometry, dissolution testing, gas chromatography (GC), and general laboratory techniques and routines.
* Experience in drafting/revising analytical protocols and reports; critical evaluation of results.
* Experience in assay, particle size distribution (PD), and dissolution testing of pharmaceutical products.
* Experience in developing analytical methods.
* Working hours: Monday to Friday, 8:00 AM to 5:00 PM, with a 1-hour lunch break
* Remuneration: R$ 11.000,00 to R$ 15.000,00 per month
* **Employment type: Independent Contractor (PJ)**
* **Work location: Barueri - SP**