Iota Diagnostic, a leading name in the medical diagnostics industry, is currently seeking qualified candidates for the role of Regulatory Affairs Executive in Gandhinagar, Gujarat. This position is ideal for professionals with experience in regulatory compliance for medical devices and diagnostics products, who are eager to contribute to innovative healthcare solutions.
Job Overview
Position: Regulatory Affairs Executive
Location: Gandhinagar, Gujarat, India
Employment Type: Full-Time, On-site
Salary: ₹30,000 – ₹41,000 per month (negotiable based on qualifications and experience)
Experience Level: Entry-Level (1-2 years in regulatory affairs within the medical devices or diagnostics industry)
Key Responsibilities
As a Regulatory Affairs Executive at Iota Diagnostic, your primary role will be to ensure that medical devices and diagnostic products comply with both Indian and international regulations. Your responsibilities will include:
- Regulatory Compliance: Ensure that all products comply with national and international regulations throughout their lifecycle.
- Liaison with Regulatory Authorities: Maintain communication with regulatory authorities to facilitate product approvals and stay updated on regulatory changes. 3. Risk Management: Participate in risk assessment and mitigation strategies related to regulatory compliance.
- Regulatory Strategy: Contribute to the development and execution of regulatory strategies to ensure timely approval of products.
- Training and Support: Provide training and support to internal teams regarding regulatory requirements and best practices
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Regulatory Affairs Executive Vacancies in Gujarat | Iota Diagnostic[/caption]
Qualifications and Skills
To be considered for the Regulatory Affairs Executive position at Iota Diagnostic, candidates must meet the following qualifications:
- Education: A Master’s degree in Pharmaceutical Science, Biomedical Devices, Medical Devices, or a related field.
- Experience: 1-2 years of experience working in regulatory affairs, particularly within the medical devices or diagnostics sector.
- Regulatory Knowledge: Familiarity with ISO 13485 standards and both Indian and international medical device regulations.
- Skills: Strong communication skills, particularly in regulatory writing and stakeholder communication. Experience in managing regulatory submissions through government portals is highly valued.
How to Apply
Interested candidates are encouraged to submit their updated resume by
12th September 2024 to
people@iotadiagnostic.com. Please use the subject line "Regulatory Affairs Executive Application" to ensure your application is processed promptly.
Location Details
Iota Diagnostic is located at
10, CrAdLE-EDII, Gandhinagar-Ahmedabad, Gujarat 382428
https://pharmastuff.org.in/job/regulatory-affairs-executive-iota-diagnostic
