Freshers Life Sciences QA Documentation Executive Job at Rivarp Medical Pvt. Ltd., Apply On Biotecnika
Job Opportunity at Rivarp Medical Pvt. Ltd.
Apply BSc, MSc from any Stream Freshers candidates required
Position: QA Documentation Executive
Department: Quality Assurance
Location: Nayandahalli, Bangalore
Salary: ₹20,000 per month
Experience: 0–1 Year (Freshers Welcome!)
Company Overview
Rivarp Medical Pvt. Ltd. is a fast-growing medical device company based in Bangalore, engaged in the design, development, and manufacturing of innovative, high-quality medical devices. Our focus spans therapeutic areas such as interventional cardiology, spine implants, and critical care. We operate in compliance with ISO 13485, EU MDR, and US FDA guidelines, offering an excellent learning platform for young professionals.
Key Responsibilities
-
Document Control
• Maintain, issue, and archive controlled documents (SOPs, protocols, work instructions).
• Support document revision, tracking, and retrieval activities as per QMS and ISO 13485 requirements. -
Quality Record Management
• Assist in preparing and organizing Batch Manufacturing Records (BMRs) and Device History Records (DHRs).
• Ensure all QA documentation is complete, verified, and audit-ready. -
Compliance & Audit Readiness
• Support activities related to change control, deviation, and CAPA documentation.
• Help QA team during internal and external audits by retrieving and preparing necessary documentation. -
QA Team Coordination
• Liaise with QA Executives and production staff to collect quality data.
• Maintain and update QA trackers using MS Excel and other tools.
Eligibility Criteria
Education:
• B.Sc. / M.Sc. in any science stream (e.g., Life Sciences, Microbiology, Chemistry, Biotechnology, Physics, etc.)
• B.E. / B.Tech in Biomedical, Biotechnology, or related fields may also apply.
Experience:
• 0–1 year (Freshers encouraged to apply)
Skills & Competencies
• Good written and verbal communication skills
• Proficiency in MS Office (Word, Excel, Outlook)
• Attention to detail and strong organizational skills
• Basic knowledge of ISO 13485 / GMP is a plus
• Willingness to learn and follow QA documentation protocols and procedures
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