Assistant Manager QC

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.),