Job Description
Job Description
This role ensures that materials and products meet strict quality standards in a regulated manufacturing or pharma environment
- Responsible for Timely analysis of under test samples giving timely results
- Coordination with tollar for quality related issues and clarification
- Sampling and analysis for RM/Intermediate/Finished Goods.
- Ensure compliance of ATR.
- Assisting team in ISO implementation
- Knowledge of calibration, standard preparation, standardization and relevant documentation.
- Handling knowledge of HPLC,GC and wet analysis
Title: QA Coordinator
Location: Carpinteria, CA 93013
Pay: $23/HR
Shift: 3pm-11:30pm
Duration: 8 months
Ongoing Functions:
- Give timely reports to SAP for result recording.
- Fill and update all documents.
- Zero accidents in the Quality operations.
- Achieving batch wise timelines, quantity and quality.
- Will train & supervise the working of all operators working in his dept. Will monitor the waste generated during operation.
- Will be member of the Emergency response team and will guide & train other team members in case of Emergency.
- Maintain ISO 9001:2008 and ISO/IEC 17025:2005, SAP, and other Quality system into department.
- Will maintain the analytical records / log sheets as per GMP & ISO guidelines
Education:
- High school diploma
Experience:
- 1-2 years of experience in Quality including cGMP, ISO and regulatory Audits
Preferred Skills/Qualifications:
- Knowledge of Quality Control in Fine Chemicals and pharmaceutical company.
- Experience of cGMP
Skills/Competencies:
- Willingness to learn
- Team Player
- Good communication skills