Brief Job Description

Analysis of raw material, stability product and new product. Documentation and preparation of lab reagent and other related lab work.

Major Accountabilities and activities

• Develop new methods and procedures.
• Ensure that Lab. cleanliness & AD equipment safety standards are maintained.
• Participate in Microbial Analysis of Lab scale, Pilot batches and stability product.
• Preparation of test solutions and volumetric solutions
• Participate in internal assessments and audits as required.
• Preparing analytical Protocol and reports based on scientific observations.
• Interpret test results, compare them to established control limits, and make recommendations.
• Participate in Departmental training.
• Ensure that Calibration of AD equipment is done.
• Compile and tabulate stability data based on observations and AD analytical tests.
• Follow up on daily, weekly, monthly and annual AD objectives.
• Preparation of calibration and verifications of analytical machines
• Conducting literature search for new method development
• Handling of AD stability registers, worksheets and other related documents and reports
• Participate in investigations of out-of-trend and out of specifications results.
• Method validation and verification.

Qualifications and Experience

Must Have: Minimum Requirements

To be considered, these minimum requirements must be evident on your resume.

• BSc. In Chem, Analytical Chem, Biochemistry, Microbiology or any other health related Science.
• 2+ years' experience of working as a Quality Control Analyst or other similar position.

• Develop new methods and procedures.
• Ensure that Lab. cleanliness & AD equipment safety standards are maintained.
• Participate in Microbial Analysis of Lab scale, Pilot batches and stability product.
• Preparation of test solutions and volumetric solutions
• Participate in internal assessments and audits as required.
• Preparing analytical Protocol and reports based on scientific observations.
• Interpret test results, compare them to established control limits, and make recommendations.
• Participate in Departmental training.
• Ensure that Calibration of AD equipment is done.
• Compile and tabulate stability data based on observations and AD analytical tests.
• Follow up on daily, weekly, monthly and annual AD objectives.
• Preparation of calibration and verifications of analytical machines
• Conducting literature search for new method development
• Handling of AD stability registers, worksheets and other related documents and reports
• Participate in investigations of out-of-trend and out of specifications results.
• Method validation and verification.

• BSc. In Chem, Analytical Chem, Biochemistry, Microbiology or any other health related Science.
• 2+ years' experience of working as a Quality Control Analyst or other similar position.