•  Location:

    Mumbai / Navi Mumbai / Thane, India

  •  Salary:

    5.00 - 10.00 Lakh / Year

  •  Experience:

    10 - 15 Year

  •  Posted by:

    about 4 years ago

Company Profile

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Headquartered in Ireland, Perrigo Company plc is a leading global healthcare supplier that develops, manufactures and distributes over-the-counter (OTC) and generic prescription (Rx) pharmaceuticals, infant formulas, nutritional products, animal health, dietary supplements, active pharmaceutical ingredients (API), and medical diagnostic products and receives royalties from Multiple Sclerosis drug Tysabri.

At Perrigo, our mission is clear, Quality Affordable Healthcare Products. An essential part of that mission, of course, is quality.

Quality is more than a concept at Perrigo, it is our most important priority. That is why we continually invest our time and resources in the quest to achieve ever higher levels of quality execution and quality products - for you, our own family members and everyone who uses our products.

Production Manager

at Perrigo Company as Fulltime

Job Description

  • To oversee the overall production or plant functions
  • To design and implement the production systems and procedures as per the USFDA requirements 
  • Smooth technology transfer of the products from Israel & Germany to Ambernath India
  • To work in close co-ordinate with perrigo teams to achieve the desired production targets with right quality & quantity standards at  Perrigo API India
  • Conceptualizing & coordinating new project activities from process point of view
  • Ensuring the implementation of high safety standards during production operations.
  • Producing APIs and, when appropriate, intermediates according to pre approved instruction.
  • Ensuring cGMP concepts with regards to overall production activity for a multipurpose plant with primary objective of producing API & intermediates 
  • Making sure that all production deviations are reported and evaluated and that critical deviations are investigated and the conclusions are recorded.
  • Design the protocols for prospective process validation, cleaning validation and prepare the reports after monitoring the entire activities
  • Review the process development documents, technology transfer documents
  • Making sure that the necessary calibrations are performed and records kept
  • Prepare master production & control records
  • Reviewing all production batch records and ensuring that these are completed and signed
  • Provide the required technical inputs / generate data for preparing & submitting the drug master files (DMF) for the APIs
  • Handle the technical queries on the product related issues
  • Perform internal audits to bring compliance
  • Evaluating proposed changes in product, process or equipment
  • Suggest improvements in the procedures and documentations. Implement the recommendations / suggestions provided by the sub ordinates
  • Handle the international quality audits
  • Reviewing of all documentation in department
  • Making sure that new and, when appropriate, modified facilities and equipment are qualified
  • Ensuring proper housekeeping in all areas of production department & plant premises

 

 

Key Skills

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