As an Assistant Manager - QC at our Haridwar location, you will be responsible for managing quality control activities related to IVD products, specifically focusing on biochemical assays and reagents. Your role will involve ensuring regulatory compliance, overseeing QC testing procedures, and collaborating with cross-functional teams. It is essential for you to have expertise in biochemistry to excel in this position. Your key responsibilities will include overseeing QC processes for biochemical assays and reagents to maintain product quality and compliance with standards such as ISO 13485 and FDA regulations. You will be required to conduct and supervise biochemical tests on raw materials, in-process items, and final products. Additionally, leading and training the QC team to ensure adherence to standard operating procedures (SOPs) will be part of your duties. You will also be responsible for ensuring that QC procedures align with regulatory requirements and preparing for audits. Collaborating with R&D, production, and QA teams to address quality issues and implementing process improvements to optimize QC workflows will also be crucial aspects of your role. To qualify for this position, you should hold a Bachelors or Masters degree in Biochemistry or a related field. You should have a minimum of 5 years of experience in QC within the IVD or medical device industry. Proficiency in biochemical testing methods like ELISA and spectrophotometry, knowledge of regulatory standards, and strong team leadership skills are essential for success in this role. If you meet the qualifications and are interested in this opportunity, please share your updated resume with us at rashi.uppal@oscarbio.com or hr@oscarbio.com. For any inquiries, you can reach out to us at 9311870576. We appreciate your interest and look forward to potential collaboration. Thank you, HR Department,
As an Assistant Manager - QC at our company, you will play a crucial role in managing quality control activities for IVD products, specifically focusing on biochemical assays and reagents. Your expertise in biochemistry will be essential in ensuring regulatory compliance, overseeing QC testing, and supporting cross-functional teams. Key Responsibilities: - Manage QC Processes: Oversee QC for biochemical assays and reagents to uphold product quality and compliance with standards such as ISO 13485 and FDA regulations. - Testing & Validation: Conduct and supervise biochemical tests on raw materials, in-process, and final products to maintain quality standards. - Team Supervision: Lead and train the QC team, ensuring strict adherence to SOPs for consistent quality control. - Regulatory Compliance: Ensure that QC procedures align with regulatory requirements and actively prepare for audits to maintain compliance. - Cross-functional Collaboration: Collaborate with R&D, production, and QA teams to address and resolve quality issues effectively. - Continuous Improvement: Identify areas for process enhancements, implement improvements, and optimize QC workflows for efficiency. Qualifications: - Education: Bachelors/Masters degree in Biochemistry or a related field. - Experience: Minimum of 5 years of experience in QC within the IVD or medical device industry. - Skills: Proficiency in biochemical testing methods like ELISA and spectrophotometry, strong knowledge of regulatory standards, and demonstrated leadership abilities. If you are interested in this opportunity, please share your updated resume with us at rashi.uppal@oscarbio.com or hr@oscarbio.com. For any queries, you can reach out to us at 9311870576. Thank you for considering this position with us. (Note: No additional details about the company were provided in the job description.),