BSc Chemistry Job at Cipla | Apply Now for Junior Officer – Packing Role
Are you looking for a BSc Chemistry Job in the pharmaceutical industry? Here is a great opportunity through Cipla Careers. Cipla Jobs has announced an opening for the position of Junior Officer – Packing in Rangpo, Sikkim. This role is ideal for candidates with a B.Pharm or BSc Chemistry who want to build their career in pharmaceutical manufacturing while working with cGMP systems, production processes, and documentation compliance.
About Cipla
Cipla is one of India’s leading pharmaceutical companies known for its commitment to innovation, quality medicines, and global healthcare solutions. Through Cipla Careers, the company provides excellent opportunities for professionals in pharmaceutical manufacturing, research, quality assurance, and production operations. Many candidates searching for BSc Chemistry Jobs and pharma industry roles consider Cipla Jobs because of its strong reputation, global presence, and employee development programs.
Job Details
- Job Role: Junior Officer – Packing
- Country: India
- State: Sikkim
- Location: Rangpo
- Req Id: 101892
This opportunity from Cipla Careers is suitable for candidates searching for BSc Chemistry Jobs in pharmaceutical manufacturing.
Job Purpose
Monitor and execute the packing activities in a shift by maintaining cGMP and safety norms to
achieve production targets.Key Accountabilities (1/6)
- 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.
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 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.
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 compliances to 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 issue (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 an average volume of 200 mn
- Average number of BPR’s handled: 200
- Average number of batches in packing: 200
- Average number of sales orders dispatched: 80
- Achieve 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 regulation
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)
This makes it an ideal BSc Chemistry Job through Cipla Careers.
Relevant Work Experience
1–5 years of experience in packing with knowledge of handling QMS activity, qualification, and other related documents.
This opportunity under Cipla Jobs is suitable for professionals with experience in pharmaceutical production and packaging operations.
