P&G was founded over 180 years ago as a simple soap and candle company. Today, we're the world’s largest consumer goods company and home to iconic, trusted brands that make life a little bit easier in small but meaningful ways. We've spanned three centuries thanks to three simple ideas: leadership, innovation and citizenship. The insight, innovation and passion of hardworking teams has helped us grow into a global company that is governed responsibly and ethically, that is open and transparent, and that supports good causes and protects the environment. This is a place where you can be proud to work and do something that matters.
Post : Product Supply Manager
Job Description
As a Product Supply Manager, you will have the opportunity to discover P&G's technologies & standards which are worldly recognized. We will help you to build your capabilities through the job experience, mentoring and training.
You are likely to be placed in one of the below functions:
1. Responsible for developing, implementing and monitoring Quality systems, procedures, and standards for on-going product and initiative delivery at P&G-owned manufacturing sites..
2.Has direct responsibility for the management of on-site Quality Assurance/Quality Control personnel and product release. Single point of contact for external and internal audits.
3. Responsible for Governance and designing end to end process of Quality compliance and Quality assurance in Injections and softgel operations.
4. Responsible for ensuring all the adequate cGMP controls are maintained as per the cGMP regulations of marketing countries.
5. Responsible for leading the USFDA and EU for the manufacturing site
6. Should be able to find the gaps against the current practices versus the requirements under USFDA and EU requirements.
7. To ensure audit readinees of the site aligning the team in audit preparation , readiness and response to the observations and defining CAPA actions.
8. Proactively shape the internal systems benchmarking with external USFDA and EU regulatory requirements.
9. Monitoring and tracking of various compliance actions that arise due to regulatory inspections and internal audits.
10. Handling internal QPHA program
11. Coordinating and implementing CSV/DI program across the site for all Quality related instruments/equipments.
12. Handling of Change control, CAPA management, Quality incidents, Market complaints , product recalls and other Quality related incidents at the site.
13. Responsible for periodic review and monitoring of Key Quality indicators of QMS.
14. Responsible for Contamination control risk and sterility assurance level.
Product Supply Planning :
• Planning and executing supply chain strategies for timely production and distribution of products to our consumers, customers and distributor partners
• Manage a team of Raw/Packed Material and Finished goods planners leading forecasting & planning for manufacturing operations of a plant / category
• Lead Cost savings and Supply Chain re-design projects for your category to improve inventory
• Coordination for distribution requirements for finished goods across plants, DC and logistics partners
• Reduce Physical distribution cost while improving service levels.
Candidate Profile
1. M Pharma /B Pharm/MSc /BSc
2. 15+ years of experience in Quality assurance in Pharmaceutical company with mandatory experience in sterile operations.
3. Expert in USFDA, EU, WHO and schedule M requirements for Drug manufacturing
4. Knowledge of USFDA and EU audits
5. Computer system validation knowledge with 21 CFR part 11
6. Sound knowledge of Quality Risk Management
7. Expertise in Clean room design requirements.
Additional Information
Location : Old Goa, Goa
Req No: R000065145
Functional Area : QA
End Date : 30th October, 2022
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