(3 Days Left) Assistant General Manager QA
2 months ago
A key objective of this position is to design, implement and enhance organizational work practices that align with quality management principles. Role will focus on establishing a culture of continuous improvement, compliance and operational excellence within the organization. Role involves the development and maintenance of a Quality Management System (QMS), managing training initiatives and driving projects related to quality and regulatory compliance within the medical device sector.
Desired Candidate Profile:
- Detail-oriented professional with 10 to 12 years of experience in Quality Assurance or related fields, preferably within the Medical Device Industry.- Strong understanding of regulatory requirements, including FDA, ISO 13485, GMP and GDP.- Proven expertise in developing and implementing QMS processes, handling compliance and conducting internal audits.- Demonstrated ability to lead quality-based projects and manage cross-functional teams.- Excellent communication and leadership skills, with a track record of successful project management and stakeholder engagement.
Responsibilities:
Quality Management System (QMS) Development:
- Design, implement, and maintain a robust QMS framework in line with regulatory requirements and industry standards.- Authorize and review SOPs, master documents, and quality protocols, ensuring comprehensive compliance across all operational processes.
Compliance & Documentation:
- Oversee the approval process for Site Master Files, Validation Master Plans, Quality Manuals, and stability summary reports.- Ensure procedural compliance in handling Change Control Notices (CCN), deviations, market complaints, Out-of-Specification (OOS) issues, CAPA, and IPQA non-conformances.- Conduct document reviews for new product launches, ensuring alignment with regulatory requirements.
Audit & Risk Management:
- Lead internal audits and self-inspections to assess compliance with quality standards and identify areas for improvement.- Investigate quality-related issues, conduct root cause analysis, and implement corrective and preventive actions (CAPA).
Project Leadership:
- Drive quality improvement projects and initiatives, collaborating with multidisciplinary teams to enhance operational efficiency and compliance.- Act as the Management Representative (MR) for quality reviews, planning and conducting Management Review Meetings (MRM), and following up on action items.
Business Continuity & Process Improvement:
- Support the business continuity management plan, ensuring seamless operations during disruptions.- Continuously monitor and improve QMS activities, including change control, deviation management, and CAPA implementation.
Training & Development:
- Identify training needs across departments and design comprehensive training programs on GMP, QMS, and regulatory compliance.- Implement and manage online training systems, ensuring consistent knowledge dissemination and compliance awareness among staff.
Functional Skills Required:
- Strong expertise in Quality Assurance, QMS implementation, and regulatory compliance.- Proficiency in managing quality projects, conducting internal audits, and performing gap analyses.- In-depth understanding of GMP, GDP, ISO 13485, and FDA regulations.- Ability to lead and manage cross-functional teams effectively.- Competence in conducting training programs and implementing quality improvement initiatives.
Behavioral Skills Required:
- Leadership and Team Management: Ability to guide, motivate, and develop team members towards achieving organizational goals.- Attention to Detail: High level of precision in reviewing documents, managing audits, and ensuring compliance.- Problem-Solving & Analytical Thinking: Strong capability to identify issues, analyze root causes, and implement effective solutions.- Communication & Interpersonal Skills: Excellent communication skills, with the ability to interact effectively with stakeholders at various levels.- Adaptability & Change Management: Ability to adapt to changing business needs and lead initiatives for continuous improvement.
Team Size to be Handle:
- Manage a team size of over 12 to 15 QA professionals, reporting directly to the Vice President of Corporate Quality.
Learn more at: is an Equal Opportunity Organisation promoting diversity while ensuring no discrimination on any ground including gender, race, religion, age, sexual orientation, disability, etc.
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