Key Objectives and Responsibilities

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  Oversee the transfer and introduction of new or modified manufacturing processes into production

  
  


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  Ensure that all aspects of the process, including equipment, raw materials, and procedures, are effectively translated into the production environment

  
  


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  Prepare and review technology transfer documentation, including validation protocols, reports, and batch records

  
  


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  Maintain documentation to ensure traceability and compliance with regulatory requirements

  
  


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  Act as a liaison between Quality Assurance (QA), Quality Control (QC), Production, Regulatory Affairs (RA) teams to ensure smooth communication and collaboration during the transfer process

  
  


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  Analyse validation data and prepare reports to support the validation process

  
  


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  Identify and resolve issues that arise during the transfer or scale-up of manufacturing processes

  
  


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  Work with manufacturing teams to optimize processes for efficiency, output, and product quality

  
  


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  Ensure that all technology transfer activities comply with Good Manufacturing Practices (GMP), regulatory guidelines, and company policies

  
  


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  Prepare necessary documentation for submission to regulatory authorities as required

  
  


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  Track project timelines and milestones to ensure that transfer activities are completed on schedule

  
  


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  Conduct risk assessments related to the transfer of processes or technologies to identify potential challenges or risks

  
  

Qualifications and Experience Required

Qualifications and Work experience

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  Bachelor’s degree of Pharmacy

  
  


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  2+ years’ experience within the Pharmaceutical Industry

  
  

Knowledge and Skills

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  Proficiency in MS Office (Excel, PowerPoint presentations)

  
  


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  High analytical mind, with exceptional problem-solving skills and attention to detail

  
  


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  Ability to work independently and collaboratively in a team environment, and adherence to cGMP and Quality Management Systems

  
  


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  A self-starter, creative, innovative, flexible and able to work well under pressure at work

  
  


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  Excellent communication skills, both oral and written

  
  

How to apply

Email your application, detailed CV and copies of academic certificates in a PDF file to; recruitment@qcil.com

Deadline for receiving applications: Wednesday 4th June 2025, at 5:00 pm.

Only short-listed candidates will be contacted. Qcil is an equal opportunity employer and therefore lobbying for the above position will lead to automatic disqualification.