BSc Chemistry Jobs at Cipla | Apply Now For the Role
Are you looking for promising BSc Chemistry Jobs with a leading pharmaceutical company? This opportunity under Cipla Careers offers hands-on exposure to cGMP-driven packing operations, advanced documentation systems, and a safe, quality-focused manufacturing environment. If you aspire to grow through impactful Cipla Jobs in India’s pharmaceutical sector, this role could be the right next step in your career.
About Cipla
Cipla is a globally recognized pharmaceutical company known for its strong commitment to quality, innovation, and patient-centric healthcare solutions. With a robust manufacturing footprint and strict adherence to regulatory standards, Cipla Careers offer long-term growth, continuous learning, and exposure to world-class systems. For candidates seeking stable and rewarding BSc Chemistry Jobs, Cipla Jobs provide an excellent platform to build a future in the pharmaceutical industry.
Job Posting Details
- Country: India
- State: Sikkim
- Location: Rangpo
- Req Id: 99290
Job Purpose
Monitor and execute packing activities during a shift, maintaining cGMP and safety standards to meet production targets.
Key Accountabilities (1/6)
- Execute shift packing activity by managing available resources and reducing microstoppages on the machine to achieve the shift target.
- Utilise shift resources optimally to get the desired production output.
- Regulate the use of consumables in the production process at an optimal level to reduce costs.
Key Accountabilities (2/6)
- 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 in accordance with GMP and safety norms by reviewing all processes and documents for compliance.
- Maintain system integrity by updating online documentation.
- Perform equipment qualification and calibration as per the schedule and update the output of all activities in the system.
Key Accountabilities (3/6)
- 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.
Key Accountabilities (4/6)
- 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 in a timely manner.
- Ensure availability and usage of PPEs in the shift by coordinating with the HSE department.
- Ensure compliance with safety training targets by monthly reconciling attendance records.
Key Accountabilities (5/6)
- 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.
Key Accountabilities (6/6)
- 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).
Major Challenges
- Meeting shift target due to the unavailability of adequate resources. Overcome by efficient workload distribution.
- Maintaining cGMP requirements during system downtime. Overcome by coordinating with the engineering and technical support team.
Key Interactions (1/2)
- 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 issues (Daily).
- Store for the daily dispensing plan and availability of packing materials (on a Daily basis).
Key Interactions (2/2)
- Maintenance contractor for any machine repairs (Need-Based).
Dimensions (1/2)
- Direct Reports : 3
- Achieve average volume of 200 mn (FY2015-16).
- Average number of BPRs handled: 200.
- Average number of batches in packing: 200.
- Average number of sales orders dispatched: 80.
- Achieve an internal OTIF of more than 90%.
- Achieve zero reportable accidents/incidents during packing activities.
- Achieve 0% errors in online documentation.
- Meet 100% compliance with SOP and Safety regulations.
Dimensions (2/2)
Key Decisions (1/2)
- Resource allocation and work distribution for each shift.
Key Decisions (2/2)
- Up-gradation in the facility and documents to the Section Head – Packing.
- Modification in equipment to Section Head – Packing.
- Deviation and implementation of CAPAs Section Head – Packing.
Education Qualification
B. Pharm. / B. Sc. (Chemistry)
Relevant Work Experience
1-5 years of experience in packing with knowledge of handling QMS activity, qualification, and other related documents.
