What are the responsibilities and job description for the QC Analyst I position at Piramal Group?
Job Overview
The QC Analyst performs analytical chemistry examination testing on raw materials, finished products or stability samples in accordance with approved Standard Operating Procedures (SOPs) and valid methods. **This position is 2nd shift** This is a safety-sensitive position.
Reporting Structure
Reports to QC Manager
Key Roles/Responsibilities
Chemical or Physical testing analysis of raw materials, finished products, stability or request samples
Documenting and submitting all raw data and results in LIMS
Preparation of reagents for chemical analysis including peer review
Knowledgeable in compendial (USP/EU) testing requirements and ensuring compliance per FDA 21 CFR
Experience
Bachelor's degree in chemistry, biology, microbiology or other related science with relevant laboratory coursework is required.
0 - 2 years laboratory experience, preferably in a GMP environment
Competencies
Basic knowledge of laboratory safety practices and PPE
Basic knowledge of cGMP
Basic understanding of good documentation practices
Understanding of compendial testing requirements
Preferred experience with FTIR, dissolution, UV-VIS, Karl Fischer, pH, wet chemistry techniques, reagent preparation, volumetric solutions.
The QC Analyst performs analytical chemistry examination testing on raw materials, finished products or stability samples in accordance with approved Standard Operating Procedures (SOPs) and valid methods. **This position is 2nd shift** This is a safety-sensitive position.
Reporting Structure
Reports to QC Manager
Key Roles/Responsibilities
Chemical or Physical testing analysis of raw materials, finished products, stability or request samples
Documenting and submitting all raw data and results in LIMS
Preparation of reagents for chemical analysis including peer review
Knowledgeable in compendial (USP/EU) testing requirements and ensuring compliance per FDA 21 CFR
Experience
Bachelor's degree in chemistry, biology, microbiology or other related science with relevant laboratory coursework is required.
0 - 2 years laboratory experience, preferably in a GMP environment
Competencies
Basic knowledge of laboratory safety practices and PPE
Basic knowledge of cGMP
Basic understanding of good documentation practices
Understanding of compendial testing requirements
Preferred experience with FTIR, dissolution, UV-VIS, Karl Fischer, pH, wet chemistry techniques, reagent preparation, volumetric solutions.
