27 Oct
Zentiva Group, a.s.
Ankleshwar
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> Job Description
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> for Executive – Quality Assurance, Pharma
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> Educational Qualification
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> - B. Pharm / M. Pharm from a reputed university
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> Experience
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> - 2 to 5 years of similar experience in regulatory-approved OSD manufacturing large units.
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> Documentation Control:
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> Preparation and Review of SOPs
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> Controlled distribution and archival of documents & records
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> Control of master documents
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> Assuring the quality of products by :
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> Ensuring SOP compliance
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> Review of Batch Manufacturing & Packing Records
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> Ensuring implementation of Corrective actions/Preventive actions proposed in Deviations and Customer complaints
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> Ensuring the effectiveness review of the implemented CAPA
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> cGMP Training :
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> To prepare training modules and organize training in GMP
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> Execute the training program in coordination with all concerned departments
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> Other:
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> Review of maintenance and calibration program
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> Diversity is a fact. Inclusion is an act @Zentiva
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> At Zentiva, we are a team of almost 5,000 unique talents bonded together by our mission to deliver high quality medicine to people whose lives depend on it. We strive daily to create a work culture where everyone feels appreciated, can be their true selves, and contribute to the best of their ability. Seeking for a balanced team across the company, we welcome applications from all qualified candidates with various educational and industry experiences, cultural or ethnical backgrounds, and different life experiences or abilities,
regardless of their religious or philosophical beliefs or whomever they choose to love.
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> To learn more about our D&I; commitment, click here.
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> Join our winning team! Be a part of our winning culture! Be Zentiva!
▶️ Executive - Quality Assurance Pharma
🖊️ Zentiva Group, a.s.
📍 Ankleshwar