Freshers QA Jobs at Rivarp Medical Pvt. Ltd. | Apply on Biotecnika
Job Title: QA Documentation Executive
Company: Rivarp Medical Pvt. Ltd.
Department: Quality Assurance
Location: Nayandahalli, Bangalore
Salary: ₹20,000 per month
Bond: 2 Years (Mandatory)
Experience: 0-1 Years
Company Overview:
Rivarp Medical Pvt. Ltd. is a fast-growing medical device company based in Bangalore, focusing on the design, development, and manufacturing of high-quality medical devices across therapeutic areas such as interventional cardiology, spine implants, and critical care.
The company adheres to international standards including ISO 13485, EU MDR, and US FDA guidelines.
Job Description:
As a QA Documentation Executive, you will support the Quality Assurance team in managing controlled documents, quality records, and regulatory files. This is an entry-level role ideal for freshers looking to begin a career in medical device quality systems, with structured training and long-term career opportunities.
Key Responsibilities:
-
Document Control
• Manage and maintain controlled copies of SOPs, Work Instructions, Protocols, and other QA documentation.
• Support the issuance, revision, and archival of documents in compliance with ISO 13485 and QMS standards. -
Record Keeping
• Assist in the preparation and filing of Batch Manufacturing Records (BMR), DHR (Device History Records), and related quality documents.
• Ensure all quality documents are complete, signed, and properly stored. -
Compliance Support
• Follow procedures related to change control, deviation, and CAPA documentation.
• Assist during internal and external audits with document retrieval and audit file preparation. -
QA Coordination
• Work closely with QA Executives and production teams to gather and verify quality records.
• Prepare and maintain QA trackers in Excel and ensure documentation is audit-ready.
Required Qualifications:
Education:
B.Sc. / M.Sc. in Life Sciences, Microbiology, Biotechnology, Chemistry, or equivalent
B.E. / B.Tech in Biomedical, Biotechnology, or related disciplines
Experience: Fresher (0–1 year) – training will be provided
Skills & Competencies:
• Good written and verbal communication skills
• Basic knowledge of ISO 13485 / GMP is a plus
• Proficiency in MS Office (Word, Excel, Outlook)
• High attention to detail and organizational skills
• Willingness to work under documentation discipline and QA protocols
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