ApoPharma, a member of the Apotex group of companies, is a pharmaceutical company devoted to the discovery, development and provision of new medicines to help improve the quality of life of patients with debilitating and life-threatening diseases. Investigation into the pathological role of iron in human disease, and how to use novel medicines to treat conditions created or worsened by iron, is a major research focus of ApoPharma.

Job Summary

Perform and report of analysis of Stability, Inprocess and Finished products, Cleaning Method validation analysis by using various analytical instruments.

Job Responsibilities Analysis of Stability, Inprocess and Finished products samples, Cleaning Method validation as per method of Analysis by adhering to the Regulatory Procedures. To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental Quality systems. Performing timely analysis of Inprocess and Finished products samples on priority basis. Performs all work in accordance with all established regulatory and compliance and safety requirements. Coordinating the issues related to the specifications/ worksheets/ other documents with concern department ans take efforts to resolve the same immeadiately.Identify the causes and recommend/implement solutions with management oversight. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned by supervisor.

 

Job Requirements Education Minimum MSc/BPharm or any equivalent degree. Knowledge, Skills and Abilities Effective command over verbal and written communication with good interpersonal skills. Command on Microsoft-Office (Word, Excel). Able to prioritize the tasks. Best in effective planning of work activities to meet the time lines. Experience Minimum 2 to 4 years of experience in GMP regulated Pharmaceutical Industry.

 

At ApoPharma, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. ApoPharma offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.