The
Raw Material Analyst (QC Chemist) is responsible to ensure all quality procedure and systems are established, implemented and followed rightly so that the company's product and services meet with regulatory norms and specifications.
Core Responsibilities
Procedures / Governance:
- Day to day assigned activities shall be performed and report to senior authority
- Any requirement related to QC shall be conveyed to reporting authority
- Testing of In process, Finished product, Raw material, Packing material, R&D sample, Reference standard, working standard & primary standard preparation, Toller samples, ETP samples, Water samples, out party samples and extra samples etc.
- Calibration activity of instruments.
- Perform Stability study analysis.
- Volumetric Solution Preparation & Standardization.
- General Cleaning of laboratory.
- Document Preparation related to laboratory.
- Stock solution preparation
- Perform Glassware Calibration
- Responsible for Instrument maintenance
- Maintain all Certificate Related to RM, Glassware
- Market complaint Sample analysis
- Sampling of RM/PM and other.
- Maintain records and logbooks of laboratory.
- Follow GLP and GDP.
- Testing sample for OOS, OOC, deviation and OOT.
- Maintain stock for chemicals and glass wares.
- Maintain control sample.
- Responsible for discard expired and extra samples
- Any job activity assigned by HOD.
- Ensure to follow safety norms.
- Ensure to wear PPE during analysis.
Training
- Impart training on Safety to new recruits, employees, contractors, contract employees.
- Periodically evaluate Training Effectiveness.
- Maintain updated records for all the Training activities.
Mandatory Requirements
Qualified candidates will have:
- Education requires, B.SC / M.SC Chemistry.
- Minimum of 5 years of experience in a quality control laboratory, preferably in the pharmaceutical industry / Chemical Industry.
- Relevant Experience in Quality Laboratory in Pharma / Chemical Industry
- English fluency, both written and spoken
Required Behaviors And Skills
- Excellent problem-solving skills and attention to detail.
- Strong communication and documentation skills.
- Ability to work independently and as part of a team
- Proficiency in analytical techniques such as HPLC, GC, and UV-Vis Spectroscopy.
- Strong understanding of cGMP, GLP, and other regulatory guidelines
- Knowledge of MS Office / Quality Reports
- Preparing Quality reports & documents
- Fluence in working with different stakeholders within a manufacturing facility within a matrix organization
- Flexibility & Agility within the organization, working at different manufacturing sites within India.
Relocation Available:
No
