Teva BPharma Job. Teva Pharmaceuticals is calling applications for Quality Sr Specialist – Apply online. B pharmacy/Msc candidates can apply for the Quality Sr Specialist at Teva Pharmaceuticals. Interested candidates can apply.
Job ID. – 49429
Job title – Quality Sr Specialist – 7212
Location – Goa, India, 403722
About the company:
Together, Teva Pharmaceuticals are on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of their medicines every single day. An amazing number, but they are always looking for new ways to continue making a difference, and new people to make a difference with.
Job responsibilities:
SAP R/3 System Handling:
- Release Blend and Bulk Finished analytical reports in SAP system.
- Print Certificate of Analysis for In-process/Finished etc. analytical reports in SAP system.
Document Review:
- Preparation and Review of other functional SOP’s
- Review of executed BMRs and BPRs, protocols, and reports.
Data integrity compliance:
- To ensure compliance with the requirements of policy and procedures on Data integrity.
- Immediate reporting of any non-compliances and observations to the superiors through QA rounds
- Handling of Glorya EDMS system for issuance of formats and related checklists
About You:
B pharmacy/Msc with 5 to 8 years of experience in QA
Hey!! Please go through the following expected question and answers during your interview preparation for the role of Quality Sr Specialist. Teva BPharma Job. All the best!!!
Can you tell us about your experience in handling the SAP R/3 system and releasing blend and bulk-finished analytical reports?
Answer: In my previous role as a Quality Specialist, I was responsible for handling the SAP R/3 system and releasing blend and bulk-finished analytical reports. I have extensive experience in navigating the SAP system, entering data accurately, and ensuring that all relevant analytical reports are released promptly. I understand the importance of maintaining data integrity and following standard operating procedures (SOPs) during this process.
How do you ensure compliance with data integrity requirements and identify non-compliances?
Answer: Data integrity is a critical aspect of quality assurance. To ensure compliance, I am well-versed in the policies and procedures related to data integrity. I actively monitor and review data for any discrepancies or irregularities. If I come across any non-compliances or observations, I promptly report them to my superiors through QA rounds. Additionally, I believe in fostering a culture of continuous improvement, where I encourage my team members to report any potential data integrity issues.
Could you describe your experience in reviewing and preparing other functional SOPs, executed BMRs and BPRs, as well as protocols and reports?
Answer: Throughout my career, I have been actively involved in the review and preparation of various documents, including standard operating procedures (SOPs), executed batch manufacturing records (BMRs) and batch packaging records (BPRs), protocols, and reports. I have a keen eye for detail and ensure that all documents are accurate, compliant with regulatory requirements, and aligned with the company’s quality standards. My experience in document control systems and my strong understanding of Good Manufacturing Practices (GMP) enable me to effectively review and prepare these critical documents.
Have you worked with a document management system such as Glorya EDMS for the issuance of formats and related checklists?
Answer: Yes, I have experience working with Glorya EDMS (Electronic Document Management System) for the issuance of formats and related checklists. I am proficient in navigating the system, uploading and updating documents, and ensuring version control. I understand the importance of maintaining a well-organized document management system to facilitate efficient document retrieval and ensure compliance with regulatory requirements.
How do you stay updated with the latest developments and regulations in the pharmaceutical quality assurance field?
Answer: As a quality professional, I believe in continuous learning and staying updated with the latest developments and regulations in the pharmaceutical industry. I actively participate in industry conferences, workshops, and seminars to gain insights into emerging trends and best practices. I also regularly review relevant publications, industry newsletters, and regulatory guidelines. Additionally, I maintain professional connections with colleagues and engage in knowledge-sharing platforms to exchange information and stay informed about the latest advancements in the quality assurance field.
Teva BPharma Job
