Key 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
• Bachelor’s degree of Pharmacy.
• 2+ years’ experience within the Pharmaceutical Industry.
• 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.
Job application procedure
Interested in applying for this job? Click here to submit your application now to recruitment@qcil.com
Email your application, detailed CV and copies of academic certificates in a PDF .Deadline for receiving applications: Friday, 30th August 2024, 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. Qcil is an equal opportunity employer and therefore lobbying for the above position will lead to automatic disqualification.
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More Information
- Address Kampala, Uganda, East Africa
