Quality Assurance Jobs & Pharma Jobs at Illusion Dental Laboratory – Apply Now
Illusion Dental Laboratory is hiring for Quality Assurance Jobs in the growing healthcare and medical device sector, offering strong career opportunities for professionals seeking Pharma Jobs in regulated quality environments. These Quality Assurance Jobs and Pharma Jobs provide hands-on exposure to ISO 13485, 21 CFR Part 820 compliance, documentation control, audits, and CAPA management across multiple locations.
Job Details
- Job Title: Quality Assurance Executive
- Job Location: Mira Road/Wada/Boisar/Kerala
About the Company
Illusion Dental Laboratory is engaged in regulated quality-driven operations within the healthcare and medical device ecosystem, supporting Quality Assurance Jobs and Pharma Jobs through compliance with ISO 13485, 21 CFR Part 820, and other applicable regulatory standards to ensure high-quality standards across operations.
Job Description
Illusion Dental Laboratory is inviting applications for Quality Assurance Jobs under the role of Quality Assurance Executive, offering excellent Pharma Jobs for professionals in regulated industries. The position focuses on supporting and enhancing the Quality Management System (QMS) in compliance with ISO 13485, 21 CFR Part 820, and other applicable regulatory standards. This role involves document control, audit support, CAPA management, and coordination with internal teams to ensure high-quality standards across operations.
Key Responsibilities
- Develop and maintain Standard Operating Procedures (SOPs) and Work Instructions in alignment with regulatory standards for Quality Assurance Jobs and Pharma Jobs
- Ensure proper document and record control in accordance with ISO 13485 and other applicable quality standards
- Participate in quality audits (internal and external) and assist in audit readiness activities
- Identify and implement corrective and preventive actions to address non-conformities
- Conduct root cause analysis as part of CAPA and complaint handling processes
- Present periodic reports on QMS performance and effectiveness to the Quality Head/Management
- Collaborate with internal departments to improve compliance and support continuous quality improvement
- Assist in setting up and improving feedback and complaint handling systems
Qualifications
- Bachelor’s and/or Master’s degree in Pharmaceutical Sciences, Engineering, Biotechnology, Microbiology, or any relevant Life Sciences discipline
- Specialization in Regulatory Affairs or Quality Assurance is preferred
Key Skills & Competencies
- Strong understanding of ISO 13485 and 21 CFR 820 requirements
- Knowledge of MDSAP standards is a plus
- Excellent documentation practices and scientific writing skills
- Familiarity with internal audit requirements; Internal Auditor certification preferred
- Good presentation and communication skills
- Ability to collaborate with cross-functional teams
Professional Experience
-
1 to 4 years of hands-on experience in Quality Assurance within a regulated industry such as Medical Devices, Pharmaceuticals, or Life Sciences
Proven experience in:
- Preparing and maintaining SOPs, Work Instructions, and other QMS documentation
- Managing document control and maintaining regulatory records
- Participating in internal and external audits
- Supporting CAPA, complaint handling, and feedback mechanisms
- Assisting in supplier evaluation, communication, and audit coordination
