Ratnamani Healthcare Pvt. Ltd. is one of the youngest and most emerging pharmaceutical player in the export market. Ratanamani Healthcare a WHO GMP certified manufacturing facility, manufactures general therapeutic and antibiotic drugs, tablets, capsules, oral liquid, dry powder and effervescent powder. It also offers contract manufacturing services to leading pharmaceutical companies. We are currently looking for candidates for the following opportunities.
๐พ๐ ๐๐๐ ๐๐๐๐๐๐.. !
We have an urgent opening for โ๐บ๐. ๐ฌ๐๐๐๐๐๐๐๐/ ๐ฌ๐๐๐๐๐๐๐๐ – ๐ท๐ท๐ฐ๐ชโ at our Indrad Plant (Near Chhatral – Kalol).
- ๐ธ๐๐๐๐๐๐๐๐๐๐๐๐๐: ย B. Pharm / M.SC /B.SC or Post Graduate
- ๐ฌ๐๐๐๐๐๐๐๐๐: 04 – 08 Years.
๐ฑ๐๐ ๐น๐๐๐๐๐๐๐๐๐๐๐๐๐๐๐:
1.ย ย ย ย Preparation of monthly Production Plan.
2.ย ย ย ย Materials Planning as per Customer Orders and Production Schedule.
3.ย ย ย ย Monitoring and Reviewing Planned V/s Actual status of Productions and Materials.
4.ย ย ย ย Co-ordination with SCM Team for Materials Order and Delivery Status.
5.ย ย ย ย Physical Stock Verification of Materials, Conducting Monthly stock count of RM/PM and inventories item.
6.ย ย ย ย Ensuring Optimum stock level as per Production Planning and maintain MAQ (Minimum Available Quantity) of materials of Regular utilizing, ย Raw materials and Miscellaneous Items in Stores Department.
7.ย ย ย ย Co-ordination with Quality Team for release of inputs.
8.ย ย ย ย Products Batch release follow up.
9.ย ย ย ย Indenting of RM and PM Materials as per the Production Plan Schedule.
10.ย Execute end-to-end process flow to start with MRP to batch release.
11.ย BMR/BPR Request to Quality Assurance.
12.ย 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 atย ๐ฐ๐ฎ๐ฟ๐ฒ๐ฒ๐ฟ@๐ฟ๐ต๐ฐ๐ต.๐ถ๐ป ๐ผ๐ฟ ๐ช๐ต๐ฎ๐๐๐๐ฝ๐ฝ ๐ผ๐ป +๐ต๐ญ- ๐๐๐๐๐๐๐๐๐๐
๐พ๐ ๐๐๐ ๐๐๐๐๐๐..!!
We are looking for โ๐บ๐. ๐ด๐๐๐๐๐๐ โ ๐ท๐๐๐
๐๐๐๐๐๐ (๐ถ๐บ๐ซ)โ at our Indrad Plant (Near Chhatral – Kalol).
- ๐ธ๐๐๐๐๐๐๐๐๐๐๐๐๐: ๐.๐๐ก๐๐ซ๐ฆ / ๐.๐๐ก๐๐ซ๐ฆ
- ๐ฌ๐๐๐๐๐๐๐๐๐: ๐๐-๐๐ ๐๐๐๐ซ๐ฌ ๐จ๐ ๐๐ฑ๐ฉ๐๐ซ๐ข๐๐ง๐๐ ๐ข๐ง ๐๐๐ (๐ ๐จ๐ซ๐ฆ๐ฎ๐ฅ๐๐ญ๐ข๐จ๐ง) ๐๐๐ ๐ฎ๐ฅ๐๐ญ๐๐ ๐๐ฅ๐๐ง๐ญ๐ฌ.
๐ฑ๐๐ ๐น๐๐๐๐๐๐๐๐๐๐๐๐๐๐๐:
1.ย Planning day-to-day activities, production schedules, execution & implementation of management plans.
2.ย Ensure manpower productivity numbers man hours / machine and batch cycle time.
3.ย Compliance to laid standard of the cGMP – Current Good Manufacturing Practices.
4.ย Exposure to Export Markets and Regulatory audits.
5.ย Aggressively drive a culture to contain issues pertaining to DATA INTEGRITY in shop floor practices.
6.ย Co-ordination for installation, qualification and validation activities as per Master Validation Plan.
7.ย ย Review of SOP , master documents of production and batch documents, etc.
8.ย Investigate and take appropriate action in case of any process deviation, non-compliance, market complaints, product failure, product recall.
9.ย ย Prepare plans for man/equipment management.
10.ย 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.ย Resolve formulation as well as equipment troubleshooting issues quickly to maintain productivity goals.
12.ย Ensuring that documentation is maintained as per GMP and other quality standards updated by the organization.
13.ย Ensuring the capacity utilization of all equipment’s in Production areas.
14.ย Proposing & Implementing Product Improvement & Operational Efficiency improvement measures.
15.ย ย Organisation of daily tasks for Formulation team, run meetings and allocate work.
16.ย Preparation of URS for new machine/equipment.
17.ย Responsible for QMS activities including change control, deviation, investigation and CAPA.
18.ย 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.
Interested candidates can share their updated CV’s atย ๐ฐ๐ฎ๐ฟ๐ฒ๐ฒ๐ฟ@๐ฟ๐ต๐ฐ๐ต.๐ถ๐ป ๐ผ๐ฟ ๐ช๐ต๐ฎ๐๐๐๐ฝ๐ฝ ๐ผ๐ป +๐ต๐ญ- ๐๐๐๐๐๐๐๐๐๐
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