Unison Pharmaceuticals Ltd – Urgently Opening for Production – OSD Packing || Apply Now
Opening for OSD Packing
2 – 5 years
Ahmedabad( Moraiya ), gujarat
This position provides front line leadership to direct reports in support of packing of drug products and drives a culture of compliance, ownership and continuous improvement with thorough working knowledge of equipment, processes and systems.
Key Accountabilities/ Responsibilities
1. All Packing Material and Manpower Handling
- Supervise cleaning activity of blister and strip machines.
- Provide training to technicians for machines, equipment operation and for line clearance activities.
- Cross check the readiness of area, machine, temperature, humidity, differential pressure and di -punch as per SOP before going for line clearance.
2. Tablet and Capsule Process
- Supervise the process of online machine activity of tablets and capsule with blister and strip packing.
- Ensure the tablets and capsules are packed in appropriate strip and blister as per the SOP.
- Provide training to technicians for operating tablets and capsule packing machines.
- Ensure pre availability/supply of tablets for strip and blister packing machine.
3. Sample Activity
- Checks the sample tablet availability in quarantine area.
- In BPR maintain batch registered for tablet sample as per the unit count
4. Manpower Handling
- Supervise the packing activity of tablet and ensure compliance to all GDP and GMP requirements.
- Support the team members in resolving problems related to machines and packing processes.
- Distribute the responsibilities among team members based on the planning.
5. Leak Test
- Supervise the full leak test activity and check machine temperature, strip pressure and vacuum pressure as per BPR.
- Maintain strip and blister in process variation and if any problem found at these stage inform to operator.
6. BPR Activities
- Perform blister cutting and coating, hologram activities and in process of strip packing.
- Enter leak test temperature and working condition in BPR
- Enter carton coding and line clearance activity related to previous product stereo restoring.
- Enter data of tablet and capsule process in BMR with date, release status, drums weight.
- Any other responsibility assigned by management in the favor of organization.
- Transfer the PVC/ Alum- alum scarp of tablets and capsule to waste room.
- Enter details and perform overall process of equipment log book.
For all the positions, candidates should also have sound knowledge cGMP documentation and must be familiar with cGMP requirements.
Interested candidates may also email their resume to email@example.com