Cipla is inviting applications for the role of Junior Officer – Production at Rangpo, Sikkim, India. This production role is suitable for candidates with a Bachelor in Pharmacy and relevant experience in pharmaceutical manufacturing, cGMP practices, and formulation production operations.
Job Details
| Company | Cipla |
| Position | Junior Officer – Production |
| Department | Production |
| Location | Rangpo, Sikkim, India |
| Qualification | Bachelor in Pharmacy |
| Experience | 3-4 years of experience with 2 years of experience in pharmaceutical manufacturing |
Job Description
The Junior Officer – Production will monitor and execute production activities in an area during the shift while maintaining cGMP and safety norms to achieve production targets. The role involves shift production execution, documentation, compliance, safety coordination, and resource management in a formulation production environment.
Key Responsibilities
- Execute production activities in a shift by managing available resources to achieve production targets.
- Carry out assigned tasks as per planned production activity to meet shift-wise production targets.
- Regulate the usage of consumables in the production process at optimum levels to save costs.
- Improve area efficiency through equipment utilization and reduction of downtime in the manufacturing area.
- Maintain standard process parameters as per BMRs and other supporting documents for achieving production targets and maintaining quality.
- Ensure all operations are performed as per GMP and safety norms by reviewing processes and documents for compliance.
- Ensure equipment, facility and block premises are maintained as per regulatory compliance requirements.
- Maintain system integrity by updating documentation and deviations on CipDox while performing operations.
- Perform validation, qualification and calibration as per schedule and update the output of all activities in the systems.
- Prepare new documents and update existing documents as per GMP requirements.
- Prepare manufacturing records and update online documentation to meet production and cGMP requirements.
- Maintain online documentation and timely entries in BMR and supporting documents.
- Operate software such as SAP, CipDox and QMS.
- Follow safe work processes and ensure safety appliances are utilised during production activities in shifts.
- Ensure safety systems and procedures are followed by operators in the shift.
- Ensure availability and usage of PPEs in the shift by coordinating with the HSE department for requirements and shift schedule.
- Coordinate with QA/QC for batch scheduling and product-related issues.
- Coordinate with Engineering and Utility teams for system-related queries.
- Coordinate with Formulation Technical Support for troubleshooting in products and with Formulation Technology Transfer for support in new products.
- Coordinate with Stores and Warehouse for RM/PM related activities.
- Coordinate with maintenance contractors, vendors and equipment manufacturers for machine repairs, spares and troubleshooting.
Qualification
- Bachelor in Pharmacy
- Knowledge of cGMP practices and equipment operations required for Formulation Production.
Experience
- 3-4 years of experience with 2 years of experience in pharmaceutical manufacturing.
How to Apply
Interested candidates can apply online through the official Cipla careers link given below.