Role & responsibilities BPCR Review, BMR Review Maintain cGMP Preferred candidate profile Need MALE candidates Perks and benefits Free Transportation from KPHB, Bala Nagar, Miyapur Canteen facility Mediclaim coverage /ESI Attendance Bonus Statutory Bonus Night shift Allowance Marriage leaves Paternity Leaves Male Maternity Leaves for female Share your resume to talentacquisition@leepharma.com

Role & responsibilities Issuing Work Permits. Maintenance of PPE Stock and Issuing to Employee. Identification of unsafe conditions and unsafe acts and take necessary actions to mitigate. Day to day checking of Spill Control Kit, Fire Hydrant, Fire Extinguishers, Fire Sand Bucket, Eye wash bottles & Eye wash fountains. Supervising Pest control activities. Recording Incidents & Accidents. Creating safety awareness among the employees. Conducting Class room and Shop floor Trainings for employees on safety. Maintaining & procuring of all critical Safety equipments, spare parts, SCBA refilling & Fire Extinguishers refilling. Monitoring of effective implementation of ISO 9001 &14001 standards. Reduce the consumption maximum, Recycle as possible as, Reuse optimum level for all natural resources Perks & Benefits Free Transportation from KPHB, Bala Nagar, Miyapur Canteen facility ESI coverage Attendance Bonus Statutory Bonus Night shift Allowance Marriage leaves Paternity Leaves Male Maternity Leaves for female Intersted candidates share your resume to talentacquisition@leepharma.com

1. Preparation and review of Drug Master Files, Dossiers as per regulatory guidelines. 2. Ensuring compliance with regulations set by the authorities. 3. Keeping up to date with changes in regulatory legislation and guidelines. 4. Analyzing complicated information & data provided by other departments, including trial data. 5. Ensuring that quality standards are met and submissions meet strict timelines. 6. Coordination with QA, QC & R&D to get documentation required for preparation of Drug Master Files & Technical dossiers. 7. Responsible for DMF/Dossier updations, revisions. 8. Responding to Customers and Regulatory Authorities on technical queries in time. 9. Maintaining customer correspondences.

Monitoring of Casual Manpower and planning. Attendance verification maintenance of Attendance for all employees and entry of permissions, leave card entry, on-duty entry etc Maintenance of Leave cards and shift wise related works. Verification of employee entry and exit. Update the logbooks on time. Coordinating in recruitment and induction of employees and other related works. Coordinating in statutory related works. Plant rounding and overall administration of of the HR Department. Monitoring the security and front office. Monthly coordinating in payroll related works. All other HR & Admin related works. Perks & Benefits Free Transportation Canteen facility ESI / Medical Insurance coverage Attendance Bonus Statutory Bonus Night shift Allowance Marriage leaves Paternity Leaves Male Preferable for Immediate joiners Interested candidates share your resume to hrdvizag@leeparma.com

Roles and Responsibilities Operate formulation machines such as FBC, blender, coating, and dryers. Ensure compliance with Good Manufacturing Practices (GMP) and Good Documentation Practice (GDP). Monitor machine performance and troubleshoot issues to minimize downtime. Maintain accurate records of production runs and quality control tests. Collaborate with team members to achieve production targets. Desired Candidate Profile 2-6 years of experience in pharmaceutical manufacturing operations or related field. Strong understanding of GMP/GDP regulations and industry standards. Proficiency in operating various types of machinery including dryers, mills, etc.