Regulatory Medical Content Specialist
5 days ago
Job Title:Regulatory Medical Content SpecialistDescription:We are seeking a skilled Regulatory Medical Content Specialist to draft, review, and finalize regulatory documents. As a key member of our team, you will perform literature reviews, adhere to regulatory guidelines, collaborate with cross-functional teams, and ensure the accuracy and quality of scientific communication.Responsibilities:Proficiency in medical and scientific writing, familiarity with regulatory document preparation, and the ability to interpret clinical and scientific data.Strong understanding of clinical study designs, statistical principles, and regulatory guidelines such as ICH-GCP and FDA/EMA standards.Excellent organizational skills, attention to detail, and the ability to meet tight deadlines.Strong collaboration and communication skills with experience working in cross-functional teams.Qualifications:Advanced degree in life sciences, pharmacy, or a related scientific field; PhD or equivalent is considered an asset.Previous experience in a similar role in the pharmaceutical, biotechnology, or clinical research industry is highly desirable.About This Role:This is a unique opportunity to join our team as a Regulatory Medical Content Specialist. If you have a strong background in medical writing and a passion for regulatory compliance, we encourage you to apply.
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Ahmedabad, India MJ Surgical Full timeWe are Hiring Regulatory Affairs Specialist For Medical Devices (Orthopedic Implants And Instruments) Role & Responsibilities: 1. Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA. 2. Work On Technical Master File. 3. Work On CERs (Clinical Evaluation Report) As Per EU MDR. 4. Work on Design & Development and Risk Management Files as...
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Ahmedabad, India MJ Surgical Full timeWe are Hiring Regulatory Affairs Specialist For Medical Devices (Orthopedic Implants And Instruments) Role & Responsibilities: 1. Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA. 2. Work On Technical Master File. 3. Work On CERs (Clinical Evaluation Report) As Per EU MDR. 4. Work on Design & Development and Risk Management Files as...
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Ahmedabad, India MJ Surgical Full timeWe are Hiring Regulatory Affairs Specialist For Medical Devices (Orthopedic Implants And Instruments) Role & Responsibilities: 1. Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA. 2. Work On Technical Master File. 3. Work On CERs (Clinical Evaluation Report) As Per EU MDR. 4. Work on Design & Development and Risk Management Files as...
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Ahmedabad, India MJ Surgical Full timeWe are Hiring Regulatory Affairs Specialist For Medical Devices (OrthopedicImplants And Instruments) Role & Responsibilities:1. Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA.2. Work On Technical Master File.3. Work On CERs (Clinical Evaluation Report) As Per EU MDR.4. Work on Design & Development and Risk Management Files as per...
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ahmedabad, India MJ Surgical Full timeWe are Hiring Regulatory Affairs Specialist For Medical Devices (OrthopedicImplants And Instruments) Role & Responsibilities:1. Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA.2. Work On Technical Master File.3. Work On CERs (Clinical Evaluation Report) As Per EU MDR.4. Work on Design & Development and Risk Management Files as per...
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Ahmedabad, India MJ Surgical Full timeWe are Hiring Regulatory Affairs Specialist For Medical Devices (OrthopedicImplants And Instruments) Role & Responsibilities:1. Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA.2. Work On Technical Master File.3. Work On CERs (Clinical Evaluation Report) As Per EU MDR.4. Work on Design & Development and Risk Management Files as per...
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Ahmedabad, India MJ Surgical Full timeWe are Hiring Regulatory Affairs Specialist For Medical Devices (OrthopedicImplants And Instruments) Role & Responsibilities:1. Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA.2. Work On Technical Master File.3. Work On CERs (Clinical Evaluation Report) As Per EU MDR.4. Work on Design & Development and Risk Management Files as per...
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Ahmedabad, India MJ Surgical Full timeWe are Hiring Regulatory Affairs Specialist For Medical Devices (OrthopedicImplants And Instruments)Role & Responsibilities:1. Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA.2. Work On Technical Master File.3. Work On CERs (Clinical Evaluation Report) As Per EU MDR.4. Work on Design & Development and Risk Management Files as per...
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Ahmedabad, Gujarat, India MJ Surgical Full time ₹ 7,20,000 - ₹ 28,80,000 per yearWe are HiringRegulatory Affairs Specialist For Medical Devices(OrthopedicImplants And Instruments)Role & Responsibilities:Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA.Work On Technical Master File.Work On CERs (Clinical Evaluation Report) As Per EU MDR.Work on Design & Development and Risk Management Files as per EU MDR.Have...
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Ahmedabad, Gujarat, India, Gujarat MJ Surgical Full timeWe are Hiring Regulatory Affairs Specialist For Medical Devices (OrthopedicImplants And Instruments) Role & Responsibilities:1. Documents Preparation for ISO13485, CE Certificate (As Per EU MDR), USFDA.2. Work On Technical Master File.3. Work On CERs (Clinical Evaluation Report) As Per EU MDR.4. Work on Design & Development and Risk Management Files as per...
