A DAY IN THE LIFE

You will be responsible for:

• Performing process validations and controls for formulation during launches, pilot batches and industrial trials.
• Performing product stability and compatibility tests for first commercial productions.
• Coordinating and overseeing process optimization projects.
• Performing analysis of bulk and management of deviations.
• Performing investigations of process nonconformities.
• Act as technical consultant to assist processing of bulks to the processing operators.
• Ensuring the quality fundamentals of plant by managing and enforcing the compliance to ISO, GMPs, DGO regulations and KEBS requirements.
• Collaborating with cross functional teams to support the plant strategies, priorities and ensure the quality culture and compliance across the plant.
• Providing onboarding, training, coaching, development, and support to ensure all employees are competent in the areas of quality.
• Managing active formulations in ERP system and raw material catalogue.
• Developing method of operation or method of manufacturing as per specification of production.
• Collaborating with safety, operations, and quality to complete risk assessment to review and mitigate risks associated with new formula production.
• Execute process validations and publish results as per the validation protocols.
• Carry out launch management to track new products to ensure product availability date.
• Actively engage in safety, quality, and performance initiatives in the plant.

REQUIREMENTS

• Bachelor of Science degree in a Technical discipline (industrial chemistry, Industrial engineering, chemical & processing engineering).
• Ability to perform the quality control, material release, nonconformance, preventative maintenance action, document & data control process and calibration process.
• 1-3 years of experience in a manufacturing environment.
• Strong communication skills.
• Knowledge of and ability to use relevant laboratory tools and equipment.
• Ability to manage and collaborate with teams.