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PHARMA JOBS POST > RATNAMANI HEALTHCARE looking for โ€œ๐‘บ๐’“. ๐‘ด๐’‚๐’๐’‚๐’ˆ๐’†๐’“ โ€“ ๐‘ท๐’“๐’๐’…๐’–๐’„๐’•๐’Š๐’๐’ (๐‘ถ๐‘บ๐‘ซ)โ€ at Indrad Plant

RATNAMANI HEALTHCARE looking for โ€œ๐‘บ๐’“. ๐‘ด๐’‚๐’๐’‚๐’ˆ๐’†๐’“ โ€“ ๐‘ท๐’“๐’๐’…๐’–๐’„๐’•๐’Š๐’๐’ (๐‘ถ๐‘บ๐‘ซ)โ€ at Indrad Plant

ADMIN
Last updated: March 6, 2022 2:02 am
ADMIN 4 years ago
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RATNAMANI HEALTHCARE looking for โ€œ๐‘บ๐’“. ๐‘ด๐’‚๐’๐’‚๐’ˆ๐’†๐’“ โ€“ ๐‘ท๐’“๐’๐’…๐’–๐’„๐’•๐’Š๐’๐’ (๐‘ถ๐‘บ๐‘ซ)โ€ at Indrad Plant

๐‘พ๐’† ๐’‚๐’“๐’† ๐’‰๐’Š๐’“๐’Š๐’๐’ˆ..!!

We are looking for โ€œ๐‘บ๐’“. ๐‘ด๐’‚๐’๐’‚๐’ˆ๐’†๐’“ โ€“ ๐‘ท๐’“๐’๐’…๐’–๐’„๐’•๐’Š๐’๐’ (๐‘ถ๐‘บ๐‘ซ)โ€ at our Indrad Plant (Near Chhatral – Kalol).

๐‘ธ๐’–๐’‚๐’๐’Š๐’‡๐’Š๐’„๐’‚๐’•๐’Š๐’๐’๐’”: ๐.๐๐ก๐š๐ซ๐ฆ / ๐Œ.๐๐ก๐š๐ซ๐ฆ
๐‘ฌ๐’™๐’‘๐’†๐’“๐’Š๐’†๐’๐’„๐’†: ๐Ÿ๐Ÿ-๐Ÿ๐Ÿ“ ๐˜๐ž๐š๐ซ๐ฌ ๐จ๐Ÿ ๐ž๐ฑ๐ฉ๐ž๐ซ๐ข๐ž๐ง๐œ๐ž ๐ข๐ง ๐Ž๐’๐ƒ (๐…๐จ๐ซ๐ฆ๐ฎ๐ฅ๐š๐ญ๐ข๐จ๐ง) ๐‘๐ž๐ ๐ฎ๐ฅ๐š๐ญ๐ž๐ ๐๐ฅ๐š๐ง๐ญ๐ฌ.
๐‘ฑ๐’๐’ƒ ๐‘น๐’†๐’”๐’‘๐’๐’๐’”๐’Š๐’ƒ๐’Š๐’๐’Š๐’•๐’Š๐’†๐’”:
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.

Interested candidates can share their updated CV’s atย ๐—ฐ๐—ฎ๐—ฟ๐—ฒ๐—ฒ๐—ฟ@๐—ฟ๐—ต๐—ฐ๐Ÿต.๐—ถ๐—ป ๐—ผ๐—ฟ ๐—ช๐—ต๐—ฎ๐˜๐˜€๐—”๐—ฝ๐—ฝ ๐—ผ๐—ป +๐Ÿต๐Ÿญ- ๐Ÿ—๐Ÿ•๐Ÿ๐Ÿ”๐Ÿ•๐Ÿ”๐Ÿ—๐Ÿ–๐Ÿ–๐Ÿ

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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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