Looking for Quality Assurance (QA) jobs in the Medical Device industry? Maven Profcon Services LLP is hiring a Junior QA – AMC Executive for its Ahmedabad office. This is an excellent opportunity for candidates with at least 6 months of Quality Assurance (QA) or Quality Management Systems (QMS) experience who want to build a career in ISO 13485, Medical Device Quality Assurance, Regulatory Compliance, and Quality Management Systems.
If you have a background in Life Sciences, Pharmacy, Biomedical Engineering, Quality Management, or related disciplines, this full-time opportunity offers hands-on exposure to global medical device quality systems, regulatory compliance, and continuous professional growth.
Job Details
| Particular | Details |
|---|---|
| Company | Maven Profcon Services LLP |
| Position | Junior QA – AMC Executive |
| Location | Makarba, Ahmedabad, Gujarat |
| Employment Type | Full-Time |
| Department | Quality Assurance / Quality Management |
| Experience | Minimum 6 Months |
| Industry | Medical Device / Regulatory Affairs / Quality Assurance |
As a Junior QA – AMC Executive, you will:
- Support implementation and maintenance of Quality Management Systems (QMS) in accordance with ISO 13485 and applicable regulatory requirements.
- Assist in preparing, reviewing, and maintaining quality documentation including SOPs, work instructions, quality manuals, and quality records.
- Coordinate with internal teams and client representatives for effective QMS implementation.
- Maintain document control systems and training records.
- Support CAPA, complaint handling, change management, and other QMS processes.
- Assist organizations in preparing for certification audits, surveillance audits, and regulatory inspections.
- Monitor updates in quality standards and regulatory regulations.
- Help implement quality system improvements for client organizations.
- Provide guidance on quality management best practices.
- Ensure compliance with international medical device quality standards.
Candidates with any of the following qualifications can apply:
- Bachelor’s Degree in Life Sciences
- Master’s Degree in Life Sciences
- Biomedical Engineering
- B.Pharm
- M.Pharm
- Quality Management
- Other related science disciplines
- Minimum 6 months of experience
- Experience in:
- Quality Assurance
- Quality Management Systems
- Medical Device QA
- Regulatory Compliance
Candidates should possess knowledge of:
- ISO 13485 Quality Management System
- CAPA
- Internal Audits
- Document Control
- Training Management
- Risk Management
- Quality Documentation
- SOP Management
- Regulatory Compliance
- Analytical and Problem-solving Skills
- Communication and Coordination Skills
- Time Management
Employees will get opportunities to:
- Work on international Medical Device projects
- Gain practical exposure to ISO 13485 implementation
- Learn global Quality Management practices
- Collaborate with experienced QA professionals
- Build expertise in Medical Device Regulatory Compliance
- Continuous learning and career development
- Work with global Medical Device and IVD companies
Makarba, Ahmedabad, Gujarat
