Chemist A - Aurobindo Pharma USA, Inc.
Dayton, NJ 08810
About the Job
Aurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical prouct development and manufacturing. Aurolife has a 10 year history of extraordinary manufacturing practices in the solid oral dose arena. The support and expertise of our parent organization has given Aurolife a jump start in building a solid pharmaceutical portfolio very quickly. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition to several formulations under manufacture, we have a robust pipeline of products. Aurolife's aim is to provide healthcare at economical prices to make this a healthier world to live in.
Job Overview:The Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of the team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level.
Responsibilities:- Perform assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per as per USP monograph / In-house / any other Compendial monographs
- Independently plan and make adequate inventory of test reagents and solutions to perform work, assure supplies are ordered as needed to perform assigned work
- Independently plan and execute testing to meet established time lines. Perform complicated testing with supervisory direction
- Record data and results as specified in documentation procedures. Document work clearly and perform tests accurately
- Prepare and/or Review Test Procedures, SOPs, and Protocols as assigned.
- Perform maintenance and calibrations of laboratory instruments/equipments with supervisory direction/training
- Perform troubleshooting and investigations under the direction of a supervisor.
- Comply with all regulatory/in-house requirements (may include but not limited to safety, house keeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity
- Review of analytical documents as required
- QC experience in the generic pharmaceutical industry is preferable
- Knowledge in Good Documentation practices. Knowledge in USP/ICH/FDA
- Ability to learn quickly and strong decision making skills
- Minimum BS within an applicable scientific field
- BS in Chemistry preferable
- Minimum 1-3 years experience in pharmaceuticals and 1-2 years experience in analytical testing desirable