Live opening · Posted 1 day ago

Manager - QA (FAN)

Panacea Biotec Limited · Baddi, Himachal Pradesh, India
Darwinbox No PERMANENT 11 - 18 Years
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At a glance

The key details from the original listing.

Posted 1 day ago
CompanyPanacea Biotec Limited
LocationBaddi, Himachal Pradesh, India
Experience11 - 18 Years
Job typePERMANENT
Work modeNo
SourceDarwinbox
Listed1 day ago

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About the role

Description supplied by the original job listing.

<p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>1. To implement quality policies and procedures and to ensure their</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>compliance in Food and Nutrition site/ Contract Manufacturing Site</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>2. To formulate Quality Management Systems to ensure cGMP / GLP / GDP</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>compliance at manufacturing, laboratory, warehouse and engineering to</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>meet current regulatory standards.</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>3. To Authorize/Approve the Standard Operating Procedures, Standard Test</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>Procedures, Specifications, Technical Documents (TDs), Protocols and</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>reports, APQRs etc.</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>4. To co-ordinate for audits by the external agencies, regulatory authorities and</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>formation of response to regulatory authorities and customers</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>5. To conduct internal quality audits to review the implementation of systems</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>as per the design to ensure cGMP compliance at site.</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>6. To ensure proper training & development of all QA personnel.</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>7. To release or reject or hold the batch of finished products for sale and</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>distribution.</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>8. To ensure the distribution, retrieval, archival, storage and retention of all</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>records related to plant.</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>9. To ensure the vendors approval and approval of contract manufacturing</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>sites as per company’s standard operating procedures including compliance</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>to quality system.</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>10. To ensure safety measures in the operation of plant.</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>11. To evaluate the performance of quality assurance department personnel.</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b style="text-indent:-0.25in;">12. Responsible for disposition and Authorization of Change Controls,</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>Incidents, Deviations, OOS, OOTs non- conformance report (NCRs) Yield</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>nonconformance report (YNCRs), market complaints and Corrective actions</b></p><p class="MsoFooter" style="margin-top:0in;margin-right:-12pt;margin-bottom:0.0001pt;margin-left:45pt;text-indent:-0.25in;line-height:115%;"><b>& Preventive Actions (CAPA).</b></p>

Experience
11 - 18 Years

Employment type
PERMANENT

Work arrangement
No

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