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Scientist, IVRT/IVPT
Location : Fairfield, NJ 07004
Experiance : 2+ Years
Posted Date : 15 July, 2020
Job Description
Stira Pharma, LLC is an emerging Contract Research and Development company provides unique range of formulation and analytical testing services to pharmaceuticals industries. We are looking for a Scientist in our IVRT and IVPT department.
Summary of Key Responsibilities:
- Conducts experiments under limited supervision and maintains excellent notebook documentation in a GMP/GLP laboratory following Good Documentation Practices and ALCOA principles.
- Performs In Vitro Release Testing (IVRT) and In Vitro Permeability Testing (IVPT) for topical formulations such as Gels, Creams, Ointments, Films and Ophthalmic Solutions as per customer needs.
- Prepares solutions for IVRT and High-Performance Liquid Chromatography (HPLC) analysis such as Mobile Phase and Buffer.
- Calibrates and operates micro and analytical balances for reference standard and reagent weighing.
- Calibrates and operates pH meter for Buffer solution adjustments.
- Operates data acquisitions system Empower 3.
- Compiles data for quantitative analyses using Empower 3 and Microsoft Excel.
- Manages daily activities in the laboratory, including chemical inventory and equipment maintenance and troubleshooting
- Safely handles and disposes of hazardous materials including Category 3 and 4 potent compounds.
- Has capacity to don half face respirator and disposable PPE for hazardous materials.
- Provides support to team members as needed.
- Works with limited supervision and interact with colleagues efficiently.
- Drafts reports, protocols, and methods
- Performs logbook and notebook review
Required Qualifications and Skills:
- S. in Pharmaceutical Sciences, Chemistry, Pharmacology, Biochemistry, Biology, or equivalent.
- 1-2 years of relevant laboratory experience, university setting or other (GMP experience is preferred).
- Possesses technical skills including handling of reference standards and topical products.
- Previous experience in dissolution and USP general chapter is preferred.
- Experience with general laboratory instruments.
- Proficiency in Microsoft Office, use of data acquisitions systems, and document management systems.
- Follows instructions meticulously, reads and executes protocols and methods as written.
- Methodical, well-organized, conscientious, and thorough
- Demonstrates logical thinking and attention to detail.
- Has the ability to work with limited supervision and interact with colleagues efficiently