- ಅನುಭವ
- 3–4 ವರ್ಷಗಳು
- ಸಂಬಳ
- —
- ತೆರೆಯುವಿಕೆಗಳು
- 1
- ಪೋಸ್ಟ್ ಮಾಡಲಾಗಿದೆ
- 2 ವಾರಗಳ ಹಿಂದೆ
- ಕೆಲಸದ ಮೋಡ್
- ಕಚೇರಿಯಲ್ಲಿ
- ವಿದ್ಯಾಭ್ಯಾಸ
- Bachelor in Pharmacy
- ಪುನರಾರಂಭ
- ಅರ್ಜಿ ಸಲ್ಲಿಸಲು ಕಡ್ಡಾಯ
ಕೆಲಸದ ವಿವರ
About the Role
The Junior Officer in Production will oversee and execute manufacturing activities within a shift, ensuring adherence to current Good Manufacturing Practices (cGMP) and safety protocols. The goal is to meet production targets efficiently while maintaining quality standards.
Key Responsibilities
- Carry out assigned production tasks during shifts to achieve set targets.
- Optimize resource and consumable usage to minimize costs and improve area efficiency by minimizing equipment downtime.
- Maintain standard process parameters based on Batch Manufacturing Records (BMRs) and related documents to assure production and quality goals.
- Enforce compliance with GMP and safety norms by reviewing processes and documentation, as well as maintaining equipment and facilities per regulatory standards.
- Update and manage system documentation, including recording deviations and performing validation, qualification, and calibration activities according to schedules.
- Prepare and update GMP-compliant manufacturing records and operate relevant software such as SAP, CipDox, and Quality Management Systems (QMS).
- Ensure safe work practices and proper use of safety gear throughout production shifts by coordinating with the Health, Safety, and Environment (HSE) department.
- Manage direct reports (approximately 12) and oversee operations across three manufacturing areas involving two dosage forms.
- Collaborate continuously with departments including QA/QC, Engineering, Formulation Technical Support and Technology Transfer, Stores and Warehouse, Safety, maintenance contractors, and equipment manufacturers to address production, quality, and maintenance issues.
Challenges
- Meeting shift production targets despite resource limitations through efficient workload distribution and resource optimization.
- Ensuring smooth knowledge transfer between shifts to avoid production lapses.
- Maintaining cGMP compliance during system downtimes via coordination with engineering and technical support teams.
Performance Metrics
- Manage approximately 35-40 production batches monthly.
- Support around 2 technology transfer projects per month.
- Achieve over 90% On Time In Full (OTIF) delivery internally.
- Year-over-year improvement in shift efficiency and zero reportable manufacturing accidents.
- Reduce batch failures and eliminate errors in online documentation.
- Ensure full compliance with Standard Operating Procedures (SOPs) and safety regulations.
Education and Experience Requirements
- Bachelor's degree in Pharmacy.
- At least 3 to 4 years of work experience including 2 years within pharmaceutical manufacturing.
- Strong understanding of cGMP practices and operational knowledge of formulation production equipment.