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![\"HaystackAnalytics](\"https:\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEgSsB5wRFsh9RDrJqm0PJ2M2rYSvjj6SCf5WoHg0hqr6oMxak16gPhlJ6LqxAb4lIHAo0-okvtzMqqHOXrR8IpQSH0abjYdwi7wRVwaM0d6CGmTY1Zi-PZWTmWemzImeSIrcnOnYTB8TiMO64fLwkof2X_4SlAzSv1y3CIFP00tsUAnlYazFoC5RWMw_vAq\/s1536\/ChatGPT%20Image%20Jul%2020,%202026,%2001_11_08%20PM.jpg\" "\\"HaystackAnalytics")
<\/a><\/div>\n\n\u2714 Verified by Medical Jobs India<\/span>\n<\/p>\n \ud83c\udfe2 HaystackAnalytics<\/p>\n \ud83d\udccd Navi Mumbai, Maharashtra<\/p>\n \ud83c\udf93 Biomedical Engg | Biotech | Life Sciences | Microbiology<\/p>\n \ud83d\udcbc Freshers & Recent Graduates<\/p>\n \u23f3 3-Month Internship | \u20b98,000 \u2013 \u20b910,000\/month Stipend<\/p>\n<\/div>\n \nAre you looking for Regulatory Affairs Internship jobs in Mumbai<\/strong>, HealthTech regulatory careers for freshers<\/strong>, or medical device compliance internships in Navi Mumbai<\/strong>? Leading genomics and HealthTech company HaystackAnalytics<\/strong> is inviting applications for a Regulatory Affairs Intern<\/strong> position at its Navi Mumbai office.\n<\/p>\n \nThis quality management system (QMS) documentation preparation, regulatory submissions support, cross-functional team coordination, and ISO 13485-aligned compliance learning internship is a 3-month paid opportunity open to freshers and recent graduates. Candidates pursuing or having completed a Bachelor’s or Master’s degree in Biomedical Engineering (preferred), Biotechnology, Life Sciences, Microbiology, or related disciplines are eligible to apply. The position offers exceptional exposure to regulatory frameworks in clinical genomics and medical device environments. To write a strong intern-level resume that highlights your academic projects, lab skills, or compliance coursework, review our guide on how to apply for healthcare and pharma jobs<\/a> online.\n<\/p>\n Educational Background:<\/strong><\/p>\n Required Competencies:<\/strong><\/p>\n \nFor freshers planning a long-term career in regulatory affairs, clinical research, or drug safety, explore our career guidance on B.Pharm & Life Sciences Careers: India vs USA<\/a>.\n<\/p>\n<\/div>\n \nBefore submitting your application, please read our step-by-step guidance on how to navigate corporate recruitment mailboxes and format your details:\n<\/p>\n \n \ud83d\udc49 Read Step-by-Step Application Guide<\/a>\n<\/p>\n<\/div>\n \nInterested freshers and recent graduates can apply by emailing their updated resume directly to the HaystackAnalytics careers team:\n<\/p>\n \nWant to build a professional, recruiter-ready resume before applying? Scan your ATS compatibility score and generate an optimized resume instantly:\n<\/p>\n \ud83d\ude80 Launch Free ATS Resume Tool<\/a>\n<\/div>\n <\/p>\n Q. Is this a paid internship at HaystackAnalytics?<\/strong> Q. What is the eligibility for this Regulatory Affairs internship?<\/strong> Q. Is prior knowledge of ISO 13485 or Regulatory Affairs mandatory?<\/strong> \ud83d\udd0e Browse More Medical Jobs<\/a>\nHaystackAnalytics Hiring Regulatory Affairs Intern \u2013 Navi Mumbai
\n<\/h2>\n\ud83d\udccb Internship Overview<\/h3>\n
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\ud83d\udcbc Key Responsibilities<\/h3>\n
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\ud83c\udf93 Eligibility Criteria & Required Skills<\/h3>\n
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\ud83c\udf81 Internship Benefits<\/h3>\n
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\ud83d\udcdd Resume Tips for Regulatory Affairs Intern Applicants<\/h3>\n
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\ud83d\udcac HaystackAnalytics RA Intern Interview Questions<\/h3>\n
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Answer Guidance:<\/em> ISO 13485 is an internationally recognized quality management system standard specifically designed for medical device manufacturers. It specifies requirements for a QMS to demonstrate the ability to provide medical devices that consistently meet customer and regulatory requirements. It is important because it is mandatory for CE marking in Europe and is widely accepted by regulators globally including CDSCO in India.<\/li>\n
Answer Guidance:<\/em> A regulatory submission is a formal package of technical, clinical, and safety data submitted to a regulatory authority (like CDSCO, FDA, or CE) for product approval or market authorization. A QMS document (such as an SOP or work instruction) is an internal operational document that defines how processes within the organization are carried out to maintain quality and compliance.<\/li>\n
Answer Guidance:<\/em> A Device Master Record or Technical File typically includes device description and specifications, design and development documentation, manufacturing process information, quality control procedures, labeling and packaging details, clinical evaluation data, and post-market surveillance records.<\/li>\n<\/ul>\n<\/div>\n\ud83d\udcd6 How to Apply?<\/h3>\n
\ud83d\udce7 Email Application Process<\/h3>\n
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\ud83d\udcc4 Try Free ATS Resume Analyzer & Builder<\/h3>\n
\u2753 Frequently Asked Questions<\/h3>\n
Yes, this is a paid 3-month internship with a monthly stipend of \u20b98,000 to \u20b910,000 per month based on the candidate’s profile.\n<\/p>\n
Freshers and recent graduates holding a Bachelor’s or Master’s degree in Biomedical Engineering (preferred), Biotechnology, Life Sciences, Microbiology, or related scientific disciplines are eligible.\n<\/p>\n
No, it is preferred but not mandatory. Freshers with a willingness to learn regulatory processes in a HealthTech environment are encouraged to apply.\n<\/p>\n<\/div>\n
\n\ud83d\udcf2 Join for Instant Job Updates<\/a><\/p>\n<\/div>\n