Roles and Responsibilities
Key Responsibilities
Ensure compliance with current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), and regulatory requirements.
Review and maintain quality assurance documentation, including batch manufacturing records, logbooks, and reports.
Monitor manufacturing and packaging activities to ensure adherence to quality standards.
Perform line clearance and in-process checks during production.
Assist in investigations related to deviations, out-of-specification (OOS) results, and customer complaints.
Support change control, CAPA (Corrective and Preventive Action), and risk assessment activities.
Participate in internal audits and regulatory inspections.
Review analytical and quality control data for compliance.
Maintain proper documentation and records as per company procedures.
Coordinate with Production, Quality Control, and other departments to ensure product quality.
Required Skills
Knowledge of GMP, GLP, and pharmaceutical quality systems.
Good documentation and report-writing skills.
Understanding of regulatory guidelines and quality standards.
Proficiency in MS Office applications.
Strong analytical and problem-solving abilities.
Good communication and teamwork skills.
Eligibility
M.Sc. Chemistry / B.Pharmacy / M.Pharmacy.
Freshers or candidates with up to 1 year of experience may apply.
Age below 26 years.
Preferred Candidate Profile
Detail-oriented with a commitment to quality.
Ability to work in a fast-paced pharmaceutical manufacturing environment.
Willingness to work in shifts if required.
Location:Nakkaplli
Employment Type: Full-Time