About Avience Biomedicals Limited: Avience Biomedicals Limited is a leading Indian organization specializing in molecular biotechnology, genomics, and in-vitro diagnostics (IVD) , with over two decades of experience in the healthcare and diagnostics sector. Headquartered in Janakpuri, New Delhi , Avience is dedicated to developing innovative, reliable, and affordable diagnostic technologies that enhance healthcare accessibility across India, particularly in rural and underserved regions. Job Summary: The Executive Secretary will provide high-level administrative, secretarial, and operational support to the Managing Director (MD) . The role involves managing daily schedules, meetings, communications, and travel arrangements while also handling office administration tasks . The ideal candidate should be proactive, well-organized, discreet, and able to manage multiple priorities efficiently. Key Responsibilities: Provide comprehensive administrative and secretarial support to the Managing Director. Manage calendar, appointments, meetings, and correspondence for the MD’s office. Draft, prepare, and manage presentations, reports, minutes of meetings, and documents . Coordinate and communicate effectively with internal departments and external stakeholders . Handle travel planning, bookings, and itineraries for the MD. Organize company meetings, conferences, and events , including outstation arrangements. Maintain confidentiality and handle sensitive business information professionally. Support office administration — procurement of supplies, vendor coordination, and facility upkeep. Assist in admin functions , including employee coordination, event planning, and record keeping. Track follow-ups, approvals, and pending tasks for the MD’s office. Be flexible for travel as required for meetings, events, or official assignments. Required Skills & Competencies: Excellent communication, coordination, and interpersonal skills . Strong organizational and multitasking abilities with attention to detail. Proficiency in MS Office (Word, Excel, PowerPoint, Outlook) and general digital tools. Ability to work independently and manage multiple priorities in a fast-paced environment. Professional demeanor, integrity, and ability to maintain confidential information . Experience working with senior leadership or in a corporate/executive support role preferred. Should be comfortable with official travel as per business requirements. Female candidates will be given preference for this role. Experience Required: 5–10 Years Educational Qualification: Graduate / Postgraduate in any discipline (Administration, Commerce, or Management preferred). Location: Janakpuri, New Delhi – 110058 (Head Office) Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Work Location: In person
Job Title: Quality Assurance (QA) Executive Location: Sector 11, Noida, Uttar Pradesh Experience Required: 5–10 years Industry: In-Vitro Diagnostics (IVD) / Medical Device Manufacturing Department: Quality Assurance About Avience Biomedicals Limited: Avience Biomedicals Limited has over 20 years of experience in molecular biotechnology, genomics and the IVD business. It is among the well-known manufacturers, suppliers and distributors of molecular diagnostics products in India. The company develops innovative, broadly-applicable solutions and works to provide affordable options for rural and under-privileged populations. Job Summary: As a QA professional at Avience Biomedicals, you will ensure compliance with regulatory standards (ISO 13485, ISO 14971, MDR, ICMED, etc.), maintain the Quality Management System (QMS), and support the manufacturing and R&D teams in producing IVD/medical devices. Your role will include documentation, audits, validations, and regulatory compliance across the organisation. Key Responsibilities: Implement and maintain the QMS in line with ISO 13485 and other relevant standards. Prepare, review, control and maintain SOPs, work instructions and quality records. Manage product documentation including Device Master Records (DMR), Device History Records (DHR) and Design History Files (DHF). Conduct internal audits and support external/regulatory audits (e.g., by certification bodies or regulatory agencies). Manage Corrective and Preventive Actions (CAPA), non‐conformance reports and change control processes. Participate in risk management activities in accordance with ISO 14971. Review and approve validation protocols and reports (equipment, process, software). Ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements applicable to IVD/medical devices. Conduct training programmes on QMS and quality procedures for cross‐functional teams. Coordinate with R&D, production and regulatory teams for product development, launch and continuous quality improvement. Required Skills & Competencies: Strong knowledge of ISO 13485, ISO 14971, EU MDR (if applicable), ICMED and GMP for IVD/medical device manufacturing. Demonstrated experience with QMS implementation, documentation control and audits. Familiarity with regulatory submissions, technical file preparation for IVD/medical devices. Excellent documentation, analytical and problem-solving skills. Proficiency in MS Office and familiarity with electronic documentation/document control systems. Strong communication and team coordination skills. Educational Qualification: B.Sc. / M.Sc. in Biotechnology, Microbiology or related Life Science field OR B.Tech / M.Tech in Biomedical / Biotechnology / Mechanical Engineering Job Type: Full-time Pay: ₹360,000.00 - ₹720,000.00 per year Application Question(s): What is your current monthly salary? What is your expected monthly remuneration? What is your Notice Period? Location: Noida, Uttar Pradesh (Preferred) Work Location: In person
Job Title: Quality Assurance (QA) Executive Location: Sector 11, Noida, Uttar Pradesh Experience Required: 5–10 years Industry: In-Vitro Diagnostics (IVD) / Medical Device Manufacturing Department: Quality Assurance About Avience Biomedicals Limited: Avience Biomedicals Limited has over 20 years of experience in molecular biotechnology, genomics and the IVD business. It is among the well-known manufacturers, suppliers and distributors of molecular diagnostics products in India. The company develops innovative, broadly-applicable solutions and works to provide affordable options for rural and under-privileged populations. Job Summary: As a QA professional at Avience Biomedicals, you will ensure compliance with regulatory standards (ISO 13485, ISO 14971, MDR, ICMED, etc.), maintain the Quality Management System (QMS), and support the manufacturing and R&D teams in producing IVD/medical devices. Your role will include documentation, audits, validations, and regulatory compliance across the organisation. Key Responsibilities: Implement and maintain the QMS in line with ISO 13485 and other relevant standards. Prepare, review, control and maintain SOPs, work instructions and quality records. Manage product documentation including Device Master Records (DMR), Device History Records (DHR) and Design History Files (DHF). Conduct internal audits and support external/regulatory audits (e.g., by certification bodies or regulatory agencies). Manage Corrective and Preventive Actions (CAPA), non‐conformance reports and change control processes. Participate in risk management activities in accordance with ISO 14971. Review and approve validation protocols and reports (equipment, process, software). Ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements applicable to IVD/medical devices. Conduct training programmes on QMS and quality procedures for cross‐functional teams. Coordinate with R&D, production and regulatory teams for product development, launch and continuous quality improvement. Required Skills & Competencies: Strong knowledge of ISO 13485, ISO 14971, EU MDR (if applicable), ICMED and GMP for IVD/medical device manufacturing. Demonstrated experience with QMS implementation, documentation control and audits. Familiarity with regulatory submissions, technical file preparation for IVD/medical devices. Excellent documentation, analytical and problem-solving skills. Proficiency in MS Office and familiarity with electronic documentation/document control systems. Strong communication and team coordination skills. Educational Qualification: B.Sc. / M.Sc. in Biotechnology, Microbiology or related Life Science field OR B.Tech / M.Tech in Biomedical / Biotechnology / Mechanical Engineering Job Type: Full-time Pay: ₹360,000.00 - ₹720,000.00 per year Application Question(s): What is your current monthly salary? What is your expected monthly remuneration? What is your Notice Period? Location: Noida, Uttar Pradesh (Preferred) Work Location: In person
About Avience Biomedicals Limited: Avience Biomedicals Limited is a leading Indian organization specializing in molecular biotechnology, genomics, and in-vitro diagnostics (IVD) , with over two decades of experience in the healthcare and diagnostics sector. Headquartered in Janakpuri, New Delhi , Avience is dedicated to developing innovative, reliable, and affordable diagnostic technologies that enhance healthcare accessibility across India, particularly in rural and underserved regions. Job Summary: The Executive Secretary will provide high-level administrative, secretarial, and operational support to the Managing Director (MD) . The role involves managing daily schedules, meetings, communications, and travel arrangements while also handling office administration tasks . The ideal candidate should be proactive, well-organized, discreet, and able to manage multiple priorities efficiently. Key Responsibilities: Provide comprehensive administrative and secretarial support to the Managing Director. Manage calendar, appointments, meetings, and correspondence for the MD’s office. Draft, prepare, and manage presentations, reports, minutes of meetings, and documents . Coordinate and communicate effectively with internal departments and external stakeholders . Handle travel planning, bookings, and itineraries for the MD. Organize company meetings, conferences, and events , including outstation arrangements. Maintain confidentiality and handle sensitive business information professionally. Support office administration — procurement of supplies, vendor coordination, and facility upkeep. Assist in admin functions , including employee coordination, event planning, and record keeping. Track follow-ups, approvals, and pending tasks for the MD’s office. Be flexible for travel as required for meetings, events, or official assignments. Required Skills & Competencies: Excellent communication, coordination, and interpersonal skills . Strong organizational and multitasking abilities with attention to detail. Proficiency in MS Office (Word, Excel, PowerPoint, Outlook) and general digital tools. Ability to work independently and manage multiple priorities in a fast-paced environment. Professional demeanor, integrity, and ability to maintain confidential information . Experience working with senior leadership or in a corporate/executive support role preferred. Should be comfortable with official travel as per business requirements. Female candidates will be given preference for this role. Experience Required: 5–10 Years Educational Qualification: Graduate / Postgraduate in any discipline (Administration, Commerce, or Management preferred). Location: Janakpuri, New Delhi – 110058 (Head Office) Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Work Location: In person