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Site Name: India - Maharashtra - Nashik Site Posted Date: Jul 5 2022 Ready to help shape the future of healthcare At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Healthcare, strengthening our leadership, and transforming our commercial execution. Now, we're making the most significant changes we've made to our business in over 20 years. We're on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science and a new world-leading consumer healthcare company of loved and trusted brands. With new ambition comes new purpose. For New GSK, this is to unite science, talent, and technology to get ahead of disease together - all with the clear ambition of delivering human health impact stronger and more sustainable shareholder returns and as a new GSK where outstanding people thrive. Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients - so we deliver what matters better and faster accountable for impact - with clear ownership of goals and support to succeed and where we do the right thing. So, if you're ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together. Responsibilities- . The incumbent is accountable & responsible for Review of Batch documents & Batch release in accordance with GSK QMS & applicable regulatory requirements and acts as the first contact point for any Quality issues in area of operation. . Ensures compliance and inspection readiness . Ensures release of bulk and finished products, meeting the statutory and QMS requirements, to market . BMR, BPR and analytical reports review and subsequent compliance review, PPA - Trending and release for finished products with performing transactions in dMERP (SAP) system. . Handling of dMERP (SAP) system related to batch release and other QA transactions to enable batch release process is followed as per SOP with status tracking & communications. . Ensures that the manufacturing & packing operations on shop floor are in compliance with regulatory and QMS requirements .
Site Name: India - Maharashtra - Nashik Site Posted Date: Jul 5 2022 Ready to help shape the future of healthcare At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Healthcare, strengthening our leadership, and transforming our commercial execution. Now, we're making the most significant changes we've made to our business in over 20 years. We're on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science and a new world-leading consumer healthcare company of loved and trusted brands. With new ambition comes new purpose. For New GSK, this is to unite science, talent, and technology to get ahead of disease together - all with the clear ambition of delivering human health impact stronger and more sustainable shareholder returns and as a new GSK where outstanding people thrive. Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients - so we deliver what matters better and faster accountable for impact - with clear ownership of goals and support to succeed and where we do the right thing. So, if you're ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together. Responsibilities- . The incumbent is accountable & responsible for Review of Batch documents & Batch release in accordance with GSK QMS & applicable regulatory requirements and acts as the first contact point for any Quality issues in area of operation. . Ensures compliance and inspection readiness . Ensures release of bulk and finished products, meeting the statutory and QMS requirements, to market . BMR, BPR and analytical reports review and subsequent compliance review, PPA - Trending and release for finished products with performing transactions in dMERP (SAP) system. . Handling of dMERP (SAP) system related to batch release and other QA transactions to enable batch release process is followed as per SOP with status tracking & communications. . Ensures that the manufacturing & packing operations on shop floor are in compliance with regulatory and QMS requirements .
Job Description :
Site Name: India - Maharashtra - Nashik Site Posted Date: Jul 5 2022 Ready to help shape the future of healthcare At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Healthcare, strengthening our leadership, and transforming our commercial execution. Now, we're making the most significant changes we've made to our business in over 20 years. We're on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science and a new world-leading consumer healthcare company of loved and trusted brands. With new ambition comes new purpose. For New GSK, this is to unite science, talent, and technology to get ahead of disease together - all with the clear ambition of delivering human health impact stronger and more sustainable shareholder returns and as a new GSK where outstanding people thrive. Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients - so we deliver what matters better and faster accountable for impact - with clear ownership of goals and support to succeed and where we do the right thing. So, if you're ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together. Responsibilities- . The incumbent is accountable & responsible for Review of Batch documents & Batch release in accordance with GSK QMS & applicable regulatory requirements and acts as the first contact point for any Quality issues in area of operation. . Ensures compliance and inspection readiness . Ensures release of bulk and finished products, meeting the statutory and QMS requirements, to market . BMR, BPR and analytical reports review and subsequent compliance review, PPA - Trending and release for finished products with performing transactions in dMERP (SAP) system. . Handling of dMERP (SAP) system related to batch release and other QA transactions to enable batch release process is followed as per SOP with status tracking & communications. . Ensures that the manufacturing & packing operations on shop floor are in compliance with regulatory and QMS requirements .
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