TECHNOLOGY TRANSFER OFFICER

  • Full Time
  • Uganda
  • Posted 3 days ago

Quality Chemical Industries

TECHNOLOGY TRANSFER OFFICER

Reports to: Quality Assurance Manager

 Key Objectives and Responsibilities

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

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

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

  • Maintain documentation to ensure traceability and compliance with regulatory requirements

  • 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

  • Analyse validation data and prepare reports to support the validation process

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

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

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

  • Prepare necessary documentation for submission to regulatory authorities as required

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

  • 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

  • Bachelor’s degree of Pharmacy

  • 2+ years’ experience within the Pharmaceutical Industry

Knowledge and Skills

  • Proficiency in MS Office (Excel, PowerPoint presentations)

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

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

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

  • 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.

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