Duties and Responsibilities 

• Assist in QC stability testing, prepare and maintain stability records and summaries.

•  Involve in training and transfer of methods to and from QC and contract manufacturers as assigned.

•  Modify and validate analytical procedures to meet QC’s needs.

•  Support design and development of experimental protocols, SOP’s, etc., consistent with cGMP/GLP.

•  Participate in special projects and department meetings via input, feedback and execution of assigned tasks.

•  Execute special projects on analytical and instrument problem solving.

•  Conduct all quality QC chemical tests.

•  Perform non radioactive and biological QC on time and record quality of product.

•  Adapt, maintain and operate analytical instrumentation.

•  Involve in procedure review and propose modifications and updates.

•  Ensure work environment is clean and safe complying with safety and pharmaceutical regulation.

•  Conduct radiation safety duties conforming to regulations.

•  Report monthly on supplies for QC orders involving devices and reagents.

•  Contribute to industrial, R&D qualification and validation activities and support routine maintenance.

•  Conduct various analytical testing procedures as per manufacturing/QC SOPs.

Job Requirements

Qualification:

•   Bachelor's  Degree in Chemistry, Science, , Biochemistry, , Pharmacy, Chemical Engineering, 

•  Skills for Quality Control Chemist

• Desired skills for quality control chemist include:

•  Advanced laboratory instrumentation and personal computer skills are critical 

How to Apply

Submit your applications by email with a cover letter, resume or CV, and copies of all qualifications and credentials. The title of your email should state the specific position you're applying for. Address your application to yonas.a@africurepharma.com