Key Responsibilities
• Ensure that cGMP is adhered to in all areas of the facility
• Assemble and review all documentation related to the processing, packing and testing of each batch of the product before authorizing for dispatch from manufacturing
• Generate, approve and issue Batch Documents
• Ensure that appropriate calibration and preventive maintenance of the manufacturing equipment is conducted as scheduled
• Ensure continuous review and upgrading of existing SOPs and work systems with respect to current guidelines
• Ensure area cleaning and line clearance during product change over, and other controls related to manufacturing, packing and stores equipment/machines/area
• Responsible for the review, approval and obsoleting master batch documents
• Perform and monitor in process checks during manufacturing and packing
• Support validation team during process, pack-line and cleaning and ensure proper documentation of the same
• Perform Pack-line Inspection and Finished Product Sampling as per procedures
• Review and monitor Pest control activities
• Oversee the environmental monitoring program to ensure the manufacturing environment meets required standards
• Participate in initiatives to improve quality systems, processes, and overall product quality
Qualifications
• Bachelor’s degree of Pharmacy, Industrial Chemistry, Pharmaceutical Science, or any other related course
• 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
• Able to work shifts on any day of the week whenever required
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.
More Information
- Address Kampala, Uganda, East Africa
