Teva Hiring B.Pharm/M.Pharm/M.sc. Graduates- Apply Online!
Teva Pharmaceuticals is currently seeking highly qualified candidates with M.Sc, B.Pharm, or M.Pharm qualifications for the position of Quality Specialist III. This role offers an exciting opportunity to join a leading pharmaceutical company and contribute to the maintenance of high-quality standards in pharmaceutical manufacturing and quality control processes. If you have a strong educational background and a passion for ensuring product quality, consider applying for this position at Teva Pharmaceuticals.
Job Title: Quality Specialist III- 6081
Company: Teva Pharmaceuticals
Location: Bangalore, India, 560064
Essential Qualification: B.Pharm, M.Pharm, M.Sc
Roles and Responsibilities:
Quality Assurance and Compliance: Ensure that manufacturing processes adhere to strict quality standards and regulatory requirements. This includes including Good Manufacturing Practices (GMP) that help to maintain product quality and safety.
Documentation and Reporting: Maintain, review, and prepare documentation related to quality control, deviations, and regulatory submissions while ensuring accurate record-keeping.
Process Improvement: Identify areas for process enhancement, collaborate with cross-functional teams, and implement corrective and preventive actions (CAPA) to continually improve product quality and efficiency.
Auditing and Risk Management: Conduct internal and external audits to assess compliance with quality standards and regulations. Actively manage and mitigate risks related to product quality and safety.
Training and Continuous Improvement: Provide training and guidance to employees. Promoting continuous improvement in quality processes throughout the organization.
Teva Hiring B.Pharm/M.Pharm/M.Sc.candidates. Here are the possible Interview Q & A that will help you:
1.Interview Question: Can you explain your experience with Good Manufacturing Practices (GMP) and how you’ve ensured compliance in your previous roles?
Answer: In my previous role at [Previous Company], I was responsible for overseeing adherence to GMP standards throughout the manufacturing process. I implemented rigorous quality control checks, conducted regular audits, and provided GMP training to staff. These measures helped us consistently meet and exceed GMP requirements, ensuring product quality and regulatory compliance.
2. Interview Question: How do you handle deviations or non-conformances in a manufacturing process? Can you provide an example of a successful deviation resolution you’ve been involved in?
Answer: When a deviation occurs, my approach is to thoroughly investigate its root cause. I document all findings, engage with cross-functional teams to develop corrective and preventive actions (CAPA), and track the progress until resolution. In my previous role at [Previous Company], we encountered a deviation related to raw material quality. Through a collaborative effort, we identified the issue, implemented CAPA, and successfully prevented its recurrence, ensuring product quality and regulatory compliance.
3. Interview Question: Describe your experience with regulatory submissions and interactions with regulatory authorities. How do you ensure timely and accurate submissions?
Answer: I have experience in preparing and submitting regulatory documents, such as INDs or NDAs, to regulatory authorities like the FDA. To ensure accuracy and timeliness, I follow a meticulous review process, engage with regulatory experts within the organization, and stay updated with evolving regulatory requirements. This approach has allowed me to contribute to successful submissions and maintain compliance.
4. Interview Question: Can you share an example of how you’ve contributed to a culture of continuous improvement in your previous role?
Answer: In my previous role, I initiated a quality improvement project aimed at reducing production waste. By collaborating with the production team and conducting data analysis, we identified areas of inefficiency. We implemented process modifications and trained employees on best practices, resulting in a 20% reduction in waste within six months. This experience highlights my ability to drive continuous improvement and foster a culture of quality excellence.
5. Interview Question: How do you stay updated with the latest developments in pharmaceutical quality and regulatory standards?
Answer: Staying updated is crucial in the pharmaceutical industry. I regularly attend industry conferences, webinars, and workshops to keep abreast of regulatory changes and emerging quality trends. Additionally, I am an active member of professional organizations such as ISPE and PDA, which provide valuable insights and networking opportunities to stay informed and contribute effectively to my role as a Quality Specialist.