Quality Control Assistant at Janta Kenya

Responsibilities

• Embrace a “team” working environment focused on achieving department goals by demonstrating willingness to accept assignments not specifically listed in the job description as allowed by the limitations of training, experience, and/or education.
• Adhere to safety rules and awareness, demonstrate good safety practices at all times. Take initiative to report and correct safety hazards. Use Personal Protective Equipment (PPE) associated with assigned tasks.
• Demonstrate and promote the values of accountability, communication, customer commitment, entrepreneurial spirit, integrity, safety and teamwork.
• Execute against project plans and goals as assigned by Quality Management.
• Meet productivity, quality and teamwork metrics for the level.
• Perform all assigned tasks according to applicable internal written procedures.
• Follow strict good documentation practices in line with company SOPs and cGMP regulation.
• Actively complete assigned training activities and document training within assigned time frames.
• Function as a subject matter expert within the analytical laboratory and provide support at all times.
•  Monitor laboratory resources, identify/report resource gaps, and assist in recruiting, screening, procuring, and/or qualifying needed resources.
• Maintain utmost level of confidentiality at all times
• Write, revise, review, and implement technical documentation including protocols, reports; reference standard qualification reports; analytical test procedures; and change controls.
• Review analytical testing records/logbooks for compliance with cGMPs, compendial requirements, and procedures/protocols.
• Review and/or write technical reports, procedures, investigations and protocols.
• Provide problem solving skills to support the resolution and documentation of investigations for laboratory and manufacturing issues.
• Draw conclusions from data and communicate those conclusions is writing.
• Determine root causes of non-conformance and recommend corrective action and ensure timely closure of investigations.
• Document, develop and apply strategies to ensure achievement of analytical objectives by monitoring/ evaluating the completion of tasks.
• Establish policies, procedures, and practices associated with laboratory activities including safety, testing, scheduling and documentation.
• Maintain and improve GMP compliance and documentation.
• Schedule laboratory testing and associated activities to minimize operational disruptions to departments.
• Perform annual review of data generated by the Quality Control Laboratory and generate data, figures and trends.
• Perform internal audits of Quality Control systems.
• Perform external audits of vendors with respect to cGMP’s.
• Determine and maintain laboratory budget.

Qualifications

• 3-4 Years working in a chemical manufacturing set up. Working familiarity with Good Manufacturing
• Practice a must.
• Experience in manufacturing of liquid bleach and analysis.

Deadline:  Monday 14th February 2022