Roles and Responsibilities
- Organizing and performing sampling and testing of all incoming supplies of raw materials that are intended for the manufacturing of different products at the site in accordance with the current approved methods.
- Monitoring the validities of the approved Raw materials and planning their re-sampling and re-testing at stipulated time intervals till the allocated expiry dates.
- Preparing material specifications and standard test methods for Raw materials in accordance with the current/established standards and requirements.
- Preparing the standard operating procedures for the activities pertinent to the sampling & testing of Raw materials.
- Maintaining the analytical records as per the Quality Control system.
- Managing the retention samples of Raw materials for future references.
- Reporting monthly KPIs of Raw material laboratory on prescribed format
- Maintaining the analytical equipment in workable conditions, to facilitate timely analysis.
Qualifications
- Bachelor’s degree in Pharmaceutical Sciences or Analytical Chemistry. An advanced Degree (master’s) in a relevant field is an advantage but not required
Experience
- 2-3 years of experience in a pharmaceutical quality control laboratory, for the testing of Raw materials.
Equal Opportunities Employer: Dei Biopharma Ltd. provides equal opportunity and fair and equitable treatment in employment to all people without regard to race, color, religion, sex, national origin, age, disability, political affiliation, marital status, or sexual orientation.
How to Apply: All interested candidates who meet the required qualifications and experience are invited to submit their CVs, Cover Letter & Academic documents (addressed to the Head of Human Capital)
