Job Description:
Operate, monitor, and maintain equipment used in the manufacturing of tablets, capsules, ointments, etc.
Follow SOPs (Standard Operating Procedures) and maintain GMP/GLP compliance.
Handle raw materials, in-process checks, and batch documentation.
Assist in scale-up, validation, and troubleshooting production issues.
Coordinate with quality assurance for batch release.
Key Responsibilities:
Execution of daily production schedules.
Maintain records of production logs and deviations.
Ensure equipment cleaning and line clearance.
Adhere to safety and regulatory standards.
Job Description:
Perform testing of raw materials, in-process samples, and finished products.
Conduct analysis using instruments such as HPLC, GC, UV, FTIR, Dissolution apparatus, etc.
Ensure compliance with pharmacopeia (IP/BP/USP/EP) specifications.
Prepare analytical reports and maintain proper documentation.
Participate in method validation and stability studies.
Key Responsibilities:
Ensure quality of product before release.
Investigate deviations, OOS (Out of Specification), and OOT (Out of Trend) results.
Maintain laboratory safety, calibration of instruments, and GLP compliance.
Support audits and regulatory inspections (USFDA, WHO, MHRA, etc.).
⚙️ Skills Required (for both):
Knowledge of cGMP & WHO guidelines.
Strong documentation and analytical skills.
Handling of pharma manufacturing / analytical instruments.
Teamwork, attention to detail, and compliance mindset.
Job Security – Pharma is a stable and ever-growing industry with consistent demand.
Career Growth – Clear progression from junior chemist/executive to managerial roles.
Skill Development – Exposure to cGMP, WHO, USFDA, and other regulatory practices.
Hands-on Experience – Opportunity to work with advanced analytical instruments / manufacturing equipment.
Global Opportunities – Experience in QC/Production opens doors in domestic & multinational pharma companies.
Good Salary & Perks – Competitive pay with allowances, PF, medical insurance, etc.
Professional Recognition – High value placed on QC/Production expertise across the pharma sector.
Contribution to Healthcare – Direct involvement in producing safe and effective medicines.