Ratnamani Healthcare Ltd Job Vacancy For B.Pharm/ BSc/ MSc/ M.Pharm

Ratnamani Healthcare Ltd Job Vacancy For B.Pharm/ BSc/ MSc/ M.Pharm

We have an urgent opening for “𝑺𝒓. 𝑬𝒙𝒆𝒄𝒖𝒕𝒊𝒗𝒆/ 𝑬𝒙𝒆𝒄𝒖𝒕𝒊𝒗𝒆 – 𝑷𝑷𝑰𝑪” at our Indrad Plant (Near Chhatral – Kalol).

𝑸𝒖𝒂𝒍𝒊𝒇𝒊𝒄𝒂𝒕𝒊𝒐𝒏𝒔: B. Pharm / M.SC /B.SC or Post Graduate

𝑬𝒙𝒑𝒆𝒓𝒊𝒆𝒏𝒄𝒆: 04 – 08 Years.

𝑱𝒐𝒃 𝑹𝒆𝒔𝒑𝒐𝒏𝒔𝒊𝒃𝒊𝒍𝒊𝒕𝒊𝒆𝒔:

1. Preparation of monthly Production Plan.

2. Materials Planning as per Customer Orders and Production Schedule.

3. Monitoring and Reviewing Planned V/s Actual status of Productions and Materials.

4. Co-ordination with SCM Team for Materials Order and Delivery Status.

5. Physical Stock Verification of Materials, Conducting Monthly stock count of RM/PM and inventories item.

6. Ensuring Optimum stock level as per Production Planning and maintain MAQ (Minimum Available Quantity) of materials of Regular utilizing, Raw materials and Miscellaneous Items in Stores Department.

7. Co-ordination with Quality Team for release of inputs.

8. Products Batch release follow up.

9. Indenting of RM and PM Materials as per the Production Plan Schedule.

10. Execute end-to-end process flow to start with MRP to batch release.

11. BMR/BPR Request to Quality Assurance.

12. Prepare Production MIS Reports, Packing List and Dispatch Plan.

13. Excellent knowledge of Advance Excel, PPT and PharmaSuite Software.

Interested candidates can share their updated CV’s at 𝗰𝗮𝗿𝗲𝗲𝗿@𝗿𝗵𝗰𝟵.𝗶𝗻 𝗼𝗿 𝗪𝗵𝗮𝘁𝘀𝗔𝗽𝗽 𝗼𝗻 +𝟵𝟭- 𝟗𝟕𝟐𝟔𝟕𝟔𝟗𝟖𝟖𝟐

We are looking for “𝑺𝒓. 𝑴𝒂𝒏𝒂𝒈𝒆𝒓 – 𝑷𝒓𝒐𝒅𝒖𝒄𝒕𝒊𝒐𝒏 (𝑶𝑺𝑫)” at our Indrad Plant (Near Chhatral – Kalol).

𝑸𝒖𝒂𝒍𝒊𝒇𝒊𝒄𝒂𝒕𝒊𝒐𝒏𝒔: 𝐁.𝐏𝐡𝐚𝐫𝐦 / 𝐌.𝐏𝐡𝐚𝐫𝐦

𝑬𝒙𝒑𝒆𝒓𝒊𝒆𝒏𝒄𝒆: 𝟏𝟐-𝟏𝟓 𝐘𝐞𝐚𝐫𝐬 𝐨𝐟 𝐞𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞 𝐢𝐧 𝐎𝐒𝐃 (𝐅𝐨𝐫𝐦𝐮𝐥𝐚𝐭𝐢𝐨𝐧) 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐞𝐝 𝐏𝐥𝐚𝐧𝐭𝐬.

𝑱𝒐𝒃 𝑹𝒆𝒔𝒑𝒐𝒏𝒔𝒊𝒃𝒊𝒍𝒊𝒕𝒊𝒆𝒔:

1. Planning day-to-day activities, production schedules, execution & implementation of management plans.

2. Ensure manpower productivity numbers man hours / machine and batch cycle time.

3. Compliance to laid standard of the cGMP – Current Good Manufacturing Practices.

4. Exposure to Export Markets and Regulatory audits.

5. Aggressively drive a culture to contain issues pertaining to DATA INTEGRITY in shop floor practices.

6. Co-ordination for installation, qualification and validation activities as per Master Validation Plan.

7. Review of SOP , master documents of production and batch documents, etc.

8. Investigate and take appropriate action in case of any process deviation, non-compliance, market complaints, product failure, product recall.

9. Prepare plans for man/equipment management.

10. Co-ordination with engineering team for effective implementation of Engineering systems for preventive maintenance and achieve higher MTBF and lower MTTR for critical machines.

11. Resolve formulation as well as equipment troubleshooting issues quickly to maintain productivity goals.

12. Ensuring that documentation is maintained as per GMP and other quality standards updated by the organization.

13. Ensuring the capacity utilization of all equipment’s in Production areas.

14. Proposing & Implementing Product Improvement & Operational Efficiency improvement measures.

15. Organisation of daily tasks for Formulation team, run meetings and allocate work.

16. Preparation of URS for new machine/equipment.

17. Responsible for QMS activities including change control, deviation, investigation and CAPA.

18. Preparation of Risk Management for New Process, System, Equipment, Impact Analysis and mitigation plan of Risk.

19. Responsible for area cleaning, online documents and compliance as per the System, SOP and Procedures.

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