Pharma Job : Manager Openings @ Zydus Cadila

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Die Hohenstein Institute bieten Prüfung, Zertifizierung und Forschung rund um das Thema Textilien – komplett aus einer Hand. Rund 4.500 Kunden weltweit profitieren von der Kompetenz der über 450 Mitarbeiter mit Stammsitz in Bönnigheim und einem weltweiten Netz von Auslandsbüros in mehr als 20 Ländern. Durch unsere Experten-Teams vor Ort können wir Ihnen unser breit gefächertes Leistungsspektrum von Textilprüfungen bis hin zur Auftragsforschung in allen bedeutenden Produktions- und Einkaufsregionen für Textilien zur Verfügung stellen. The Hohenstein Institute carries out testing, certification and research in the field of textiles - all under one roof. About 4,500 customers all around the world benefit from the expertise of the more than 450 employees who are either based at the headquarters in Bönnigheim (Germany), or in a global network of branch offices in more than 20 different countries. Thanks to our expert local teams, we can offer you our wide-ranging portfolio of services to vary from textile testing to contract research in all the main textile producing and purchasing regions of the world.

Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. The group has state-of-the-art vertically integrated manufacturing facilities for APIs and Formulations, spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim.

Job Title – Dy. Manager – Manufacturing Excellence and Investigator

No.of.Openings – 2

Experience – 5 – 10 Years

Location – Panjim/Panaji

Job Description:

A. Manufacturing Excellence (1 Position) :

  • Responsible for manufacturing excellence initiatives at plant level.
  • Responsible for taking initiatives in improvement of all aspects of working processes and methodologies.
  • Predictive analytics improvement of operational parameters like Yield, cycle time, equipment efficiency, Process Cycle Efficiency, CPP trending etc.
  • Leading the OEE (Overall Equipment Efficiency) program for the formulation plants to diagnose and identify opportunities to improve OEE.
  • Architect for Lean Six Sigma framework.
  • Having experience in Process capability Improvement, DMAIC/8D methodology, Statistical analysis and other Operational Excellence tools. Should be acquainted with application like Minitab , Visio and Quality Companion.
  • Must have worked in regulated plants having approvals of US FDA, MHRA. etc.
  • Hands-on experience in handling and implementing cGMP (Current Good Manufacturing Practice) practices and Good Documentation Practices.
  • Technically competent on all aspects of Tablet /capsule manufacturing with FDA approval.

B. Investigator/Trouble shooting (1 Position)

  • Relevant experience of IPQA Activities / QMS/
  • Assessment of change controls relating to risk management and gap analysis.
  • Preparation and review of Failure Investigation Reports against Quality Impacting deviations, Out-of-Specifications and major Non-Conformances.
  • Market Complaints and Regulatory Audit observations / Identification of scope for implementation of Preventive Action to mitigate or reduce risk of recurrence in oral solid dosage/ Injectable Manufacturing facilities.
  • Must have worked in regulated plants having approvals of US FDA, MHRA. etc.
  • Hands-on experience in handling and implementing cGMP (Current Good Manufacturing Practice) practices and Good Documentation Practices.

 

Desired Profile:

  • UG – B.Pharma – Pharmacy 
  • PG – M.Pharma – Pharmacy

Click here to Apply Online

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