Summary
Date Posted: Monday, October 30 2023, Base Salary: Not Disclosed

JOB DETAILS:
DUTIES AND RESPONSIBILITIES
• Provide guidance to development, operations, laboratories, and validation groups for compliance with quality standards and regulatory requirements such as GMP and GLP.
• Conduct regular reviews and approvals of records, reports, and completed tasks for accuracy and adherence to procedures, ensuring the timely release of tasks.
• Collaborate with development teams during design and prototyping, participating in reviews to ensure products meet quality requirements.
• Support operations teams in implementing and maintaining quality control measures on the production floor through periodic inspections.
• Work closely with laboratory teams to ensure testing protocols and procedures meet quality standards; review and approve laboratory reports for accuracy and compliance.
• Oversee the validation of equipment, processes, and systems, reviewing and approving protocols and reports to ensure regulatory compliance.
• Identify and implement opportunities for process improvements, collaborating with cross-functional teams to enhance the overall quality management system.
• Provide training to employees on quality systems, procedures, and regulatory guidelines. Ensure that all personnel involved in manufacturing and quality processes are aware of their responsibilities.
• Participate in internal and external audits, responding to audit findings and implementing corrective actions especially related to quality control tests, procedures, and laboratory equipment

Qualifications & Experience
• Pharmacy/Biomedical Engineering/Chemical Engineering/Biology/Biotechnology
• Bachelor’s degree in a relevant field (e.g., Quality Management, Engineering, Life Sciences).
• Knowledge of the production SAP is an added advantage
• Proven experience of 7 years in quality assurance within the medical equipment manufacturing industry.
• Strong knowledge of regulatory requirements such as NDA, WHO and ISO 13485, ISO 9001.
• Strong analytical and problem-solving skills.
• Excellent communication and collaboration skills.
• Proficient in MS Office suite ie Word, Excel, Power-point.


Work Hours: 8

Experience in Months: 84

Level of Education: Bachelor Degree

Job application procedure
Visit Q-Sourcing website www.qsourcing.com/jobs-in-Uganda  and follow the link on the position to submit your application and CV merged into one document. "Deadline for submissions is Tuesday 07th Nov 2023 at 5:00 pm EAT. NOTE that only successful candidates will be contacted. Direct or Indirect Canvassing will lead to automatic disqualification. Hardcopy applications will not be accepted


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