The Quality Control Analyst – Finished Product will be responsible for the Testing of semi-finished, finished products and stability samples in the Quality Control laboratory in an effective, efficient and compliant manner and to report test results in a timely manner and maintain a state of GMP Compliance in the Laboratory.

Start date: Candidate must begin working within a reasonable period.

Roles and Responsibilities

1. Perform the chemical analysis of samples of Semi-Finished and Finished product in accordance with current approved standard test methods and specifications.
2. Perform the chemical analysis of stability samples kept at accelerated and long-term conditions in accordance with current approved standard test methods.
3. Prepare the stability protocols of samples of products
4. Help out the team leader for the management of inventory of lab consumable, like reagents and HPLC columns, to facilitate smooth testing of samples of products.
5. Perform analytical method validations.
6. To prepare the Standard testing method and specifications for finished products.
7. To prepare the standard operating procedures relevant to quality control systems.
8. To report monthly KPIs of finished product testing on prescribed format.

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 finished products.

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.