Cipla is hiring for a Junior Officer-Packing Role | Pharmacy Graduates Apply Now
If you are searching for a Pharma Job, exciting opportunities are available through Cipla Careers for the role of Junior Officer – Packing in Rangpo, Sikkim. This role is ideal for candidates with a B.Pharm qualification and experience in pharmaceutical packing operations. Through Cipla Careers, professionals can build strong expertise in cGMP-compliant environments while contributing to safe and efficient packing operations in the pharmaceutical industry.
- Job Title: Junior Officer – Packing
- Location: Rangpo
- Req ID: 101892
About The Company
Through Cipla Careers, professionals get the opportunity to work with one of the leading pharmaceutical organizations known for its commitment to quality, innovation, and regulatory compliance. Cipla focuses on maintaining global cGMP standards, safe manufacturing environments, and efficient pharmaceutical operations to deliver high-quality medicines worldwide. A Pharma Job at Cipla provides excellent exposure to modern pharmaceutical manufacturing and packing processes.
Key Responsibilities
In this Pharma job, you should monitor and execute the packing activities in a shift by maintaining cGMP and safety norms to achieve production targets.
- Execute shift packing activity by managing available resources and reducing micro stoppage of the machine to achieve the shift target.
- Utilise shift resources optimally to get the desired production output
- Regulate the usage of consumables in the production process at an optimum level to save cost
- Review documentation related to packing activity and monitor standard packing parameters as per BPR to meet regulatory requirements.
- Review and monitor critical in-process parameters like NFD, camera challenge, RH temperature, etc.
- Review and perform all operations as per GMP and safety norms by reviewing all processes and documents for compliance
- Maintain system integrity by updating online documentation
- Perform qualification and calibration of equipment as per the schedule, and update the output of all activities in the system
- Prepare manufacturing records and update online documentation to meet production and cGMP requirements.
- Maintain online documentation and timely entries in BPR and supporting documents by operating SAP and CIPDox
- Prepare new documents and update existing documents as per GMP requirements
- Monitor adherence to safety guidelines in the block during a shift for packing activities to create a safe working environment.
- Monitor safety systems and ensure procedures are followed in shift and near-miss cases are reported to HSE promptly
- Ensure the availability and usage of PPEs in the shift by coordinating with the HSE department
- Ensure compliances to safety training targets by monthly reconciling attendance records
- Provide training to staff & workmen for packing activity by regular interactions with them to get quality product.
- Provide training to staff and daily workers for packing activities and safety procedures
- Conduct training related to equipment handling, cGMP, documentation, and unit operations
- Provide new ideas and simplify processes to reduce process cycle time and achieve new targets.
- Provide new ideas during idea sessions for better productivity with minimum cost
- Identify the complexities and suggest process simplification areas to achieve the new target with optimum utilization of resources
- Reduce and simplify documentation for better accuracy and to meet ALCOA (Attributable Legible Contemporaneous Original Accurate).
Key Interactions
- Quality assurance and control for batch release as per the packing plan (Daily)
- Engineering for preventive maintenance and help in modification (as per need)
- Safety for awareness training and near miss issue (Daily)
- Store for the daily dispensing plan and availability of packing materials (daily)
-
Maintenance contractor for any machine repairs (Need-Based)
Qualifications
- B. Pharm
Relevant Work Experience
- 1–5 years of experience in packing with knowledge of handling QMS activity, qualification, and other related documents.
