Sandoz Hiring D Pharm / B Pharm Candidates for Operative Executive Production Post
Sandoz Hiring D Pharm / B Pharm Candidates for Operative Executive Production Post. interested Candidates check out the details below and Apply online
Job Position: Operative Executive Production ONCO
Job Location: Navi Mumbai, India
Job id: 380036BR
Job Category: Technical Operations
Job Type: Full Time
Job Description
Position Purpose:
- Operate equipment/s and execute assigned manufacturing tasks and activities according to production schedule to enable the timely production of products. Manage & overseeing compliance to all relevant cGMP documentation for the product being manufactured with the relevant GMP, safety and environmental guidelines.
- Perform routine operational support activities according the manufacturing process and schedule and enable the timely production of product with the quality and quantity an ensure that all activities and documentation comply with the requirement of safety, GDP/GMP, Data Integrity standards.
- Manage and oversee the modification, editing, distribution, review and archiving of GMP manufacturing documents and the edition of the Batch records in order to deliver them to Production in the quality and within the deadlines.
- Share knowledge and develop expertise of others and understanding of applied practice and processes in own area/discipline. Follow up to ensure production equipment to work properly with planned capacity in his/ her responsibility area.
- Ensure proper escalation of all matters related with HSE, quality, supply and production, implement decisions and act as responsible for continuity of production. Identify, assure and implement continuous improvement initiatives, which sustain Novartis competitive advantage.
- Actively participate collaborate with a trouble-shooting team to Ensure that the potential or actual process problems are correctly identified, and effectively resolved. Responsible for personal and professional development and support building organizational culture in line with Novartis values and behaviors.
 key responsibilities:
• Equipment Operator, Participation to the manufacturing processes. Execution of all assigned activities according to production schedule and in compliance with the valid GMP, work, operating, environmental and safety instructions and guidelines. Execution of all assigned activities in compliance with the GMP, occupational safety and environmental guidelines
• Service Operator, Participation to the manufacturing support processes. Execution of all assigned activities according to production schedule and in compliance with the valid GMP, work, operating, environmental and safety instructions and guidelines.
• Willingness to continuously improve and analyze weak points, Documentation Admin, Prepare, print and consolidate the batch documents, labels.
• Follow up on updates and versions of documents in production (procedures and logbooks), Batch record system administration. Create and manage revisions of MBR in case of paper based records.
• Ensure and coordinate the updating of production documents (forms, SOPs, logbooks etc.), HSE and Quality.
• Promote and improve the Safety and Quality cultures, Apply in practical the upgrading, and the improvement of Safety and Quality on the shop floor. Ensure overall inspection readiness for area of responsibility.
Minimum Requirements:
• D. Pharm / B. Pharm.
• Minimum 5 to 6 years of experience in OSD Oncology facility in reputed Pharmaceutical Company handling various equipment and production process.
• Operations Management and Execution
• Collaborating across boundaries
• Functional Breadth
Sandoz Hiring D Pharm / B Pharm Candidates for Operative Executive Production. Here are five Possible interview questions and answers :
1. Question: Can you describe your experience in handling manufacturing processes and equipment in an OSD Oncology facility?
Answer: Absolutely. Over the past 5 to 6 years, I have gained valuable experience in handling various equipment and executing manufacturing processes in an OSD Oncology facility. My responsibilities have included operating equipment, following production schedules, and ensuring compliance with GMP, safety, and environmental guidelines. I have been involved in the execution of assigned activities, batch record management, and ensuring quality and quantity in production. I am well-versed in the intricacies of the manufacturing processes in this specific domain.
2. Question: How do you ensure compliance with GMP, safety, and environmental guidelines during the manufacturing process?
Answer: Compliance with GMP, safety, and environmental guidelines is of utmost importance in a pharmaceutical manufacturing setting. I ensure compliance by meticulously following all standard operating procedures (SOPs), work instructions, and guidelines provided by the company. Regular training and staying updated on any changes or revisions to protocols are crucial. Additionally, I actively participate in promoting a culture of safety and quality on the shop floor, encouraging others to do the same and implementing continuous improvement initiatives to maintain compliance.
3. Question: Can you tell us about a specific challenging situation you encountered during a manufacturing process and how you resolved it?
Answer: During a critical manufacturing process, we faced an unexpected issue with one of the key pieces of equipment. It could have caused delays in production and affected the product’s quality. To resolve the situation, I promptly alerted the relevant team members, including maintenance and production supervisors. While the equipment was being fixed, we utilized alternative equipment and adjusted the production schedule to minimize any potential disruption. Clear communication and collaboration with the troubleshooting team allowed us to identify the root cause and implement corrective measures swiftly, ensuring a successful outcome.
4. Question: How do you stay updated on changes or revisions to manufacturing documents and batch records?
Answer: Staying updated on manufacturing documents and batch records is vital for maintaining compliance and ensuring smooth operations. I actively monitor any updates or versions of procedures and logbooks related to production. Additionally, I am responsible for creating and managing revisions of Master Batch Records (MBR) in case of paper-based records. I collaborate with the relevant departments to ensure timely updates and effective communication of changes to all stakeholders involved in the production process.
5. Question: How do you promote a culture of safety and quality in the manufacturing environment?
Answer: Promoting a culture of safety and quality is a shared responsibility among all team members. To contribute to this culture, I actively lead by example, following all safety protocols and best practices myself. I encourage open communication among team members, allowing them to report any safety concerns without fear. Regular safety training sessions and workshops are organized to reinforce safety practices and address any queries. Quality is emphasized through a rigorous adherence to GMP guidelines and continuous improvement initiatives, which I actively participate in and support.
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