Associate, Quality Processes, Johannesburg

At Dr. Reddy’s, a global pharmaceutical company, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier lives. Weare seeking dynamic and energetic individuals ready to inspire, ready to make a difference for their community and every community.Job Description

We are seeking a detail-oriented and analytical Associate, Quality Processes to join our team in Johannesburg, South Africa. In this role, you will collaborate with various departments to ensure quality oversight of equipment, systems, and processes in our pharmaceutical manufacturing facility. You will play a crucial role in maintaining and improving our quality standards while adhering to industry regulations.Conduct and document root cause investigations for customer product quality complaints in accordance with SOPs and industry guidelines Perform internal audits to ensure compliance with cGMP, FDA regulations, and ICH guidelines Assist in analyzing data for trends and present findings in monthly quality reviewsSupport the collection and summarization of data for annual product reviews Contribute to stability program management, including study initiation, sampling, and data compilation Collaborate with peer departments in managing Corrective and Preventive Actions (CAPAs) Provide quality oversight for manufacturing floor operations as neededAssist with vendor audits and qualification processes Participate in root cause deviation investigations of non-complex issues Support the development and improvement of quality processes and procedures Qualifications

Bachelor's degree in a science field related to pharmaceutical product manufacturing and testing 3-5 years of experience in a Pharmaceutical Quality role or Product Disposition Strong knowledge of cGMP, FDA regulations, and ICH guidelines Demonstrated experience with quality management system elementsExcellent attention to detail and commitment to accuracy and completeness in decision-making Ability to work efficiently with strict timelines and adapt to changing priorities Strong interpersonal skills with a proven ability to work collaboratively in a team environment Capability to work independently and without direct supervision when requiredExcellent written and oral communication skills Experience and proficiency in root cause analysis tools and techniques Strong computer skills, including proficiency in statistical applications SAP experience preferred Flexibility to work occasional overtime and shifts as per business needs Analytical mindset with a focus on continuous improvementFamiliarity with stability testing procedures and data analysis Additional Information

All your information will be kept confidential according to EEO guidelines.

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