Regulatory Affairs and Scm
4 days ago
**Job Title**:Regulatory Affairs and SCM -Executive
**Location**:Chennai, India**Employment Type**:Permanent**About OMRON**
- Founded in 1933, OMRON has come a long way since and has evolved to become an organization committed to creating new social values. Today, In the APAC region, OMORN has a strong presence in Industrial Automation, Healthcare, and Device & Module Solutions. Let’s begin the exciting journey of Shaping Future 2030 together with us**About OMRON Healthcare Business**
- With a vision “To advance health and empower people worldwide to live life to the fullest”, OMRON’s
- **Healthcare Business **produces internationally acclaimed and certified medical devices such as Digital Blood Pressure Monitors, Thermometers, Nebulizers, devices related to pain and weight management etc. Understand more about our
- **Healthcare Business** HERE.Short Description
**Responsibilities**:
**Regulatory Affairs**
1. Receive and supervise the incoming medical device and ensure quality and standards of these devices and supplies are as per the Indian regulatory requirements.
2. Monitor and maintain the data as per CPCB requirement for the dispose-off as per Plastic waste management rule and in future to comply with battery waste and upcoming e-waste management regulations by Central pollution control board.
3.Arrange for distribution of the medical devices to various destinations by signing the invoices.
4.Maintain the lifecycle of WH regulatory approvals, licenses, registrations by getting renewed before due time.
5. Produce reports and statistics during audits by State Drug Authority, Government bodies and other agencies.
**Supply Chain Management**
1. Support SCM team on inventory control system, participate in monthly inventory blind inventory check conducted by WH partner company. Analyze if any inventory inaccuracies by WH partner vs Omron and report.
2. Check on in transit Inventory, check weekly pallet WH reports and analyze weekly W.H. pallet capacity vs weekly ETA shipments and share report with SCM INC manager.
3. Support WH team and prepare analysis on dispatched SOCs DSR last mile delivery status. Set Monthly WH meetings to review logistics KPIs.
**Job Requirements**:
**Job Location**:Chettipedu Village, Mevaloorkuppam, Thandalam, Panchyat Sriperumbudur Taluk, Chennai
- 602105
Diploma or degree holder in pharmaceutical science with 2 years’ experience as a competent person in Retail, Pharma or medical device industry.
Must have the pharmacy council registration certificate from the state drug authority in Chennai.
Proficient in the English and local language, both written and verbal. Good knowledge of Microsoft Office (Word, Excel, PowerPoint). Possess strong Negotiation Skills
**Why Join us**
- OMRON’s mission is to improve lives and contribute to a better society. We endeavor to make our diverse workforce feel equally valued and enjoy equal opportunities to help us achieve so. So come, work with the best of the best teams, collaborate, and innovate together with diverse, capable minds across the globe.**Req ID**:1408
-
Regulatory Affairs Executive
1 week ago
Ambattur, Chennai, Tamil Nadu, India Gesco Healthcare Pvt Ltd Full timeCompany Description GESCO Healthcare is a leading manufacturer and exporter of spinal, orthopaedic, and CMF implants and surgical instruments in the Asia-Pacific region. With over 60 years of experience, GESCO has transformed the lives of over 120 million people. The company's innovation center leads the way in developing path-breaking and cost-effective...
-
Regulatory Affairs Executive
2 weeks ago
Ambattur, Chennai, Tamil Nadu, India Gesco Healthcare Pvt Ltd Full timeCompany Description GESCO Healthcare is a leading manufacturer and exporter of spinal, orthopaedic, and CMF implants and surgical instruments in the Asia-Pacific region. With over 60 years of experience, GESCO has transformed the lives of over 120 million people. The company's innovation center leads the way in developing path-breaking and cost-effective...
-
Regulatory Affairs Officer
1 week ago
Egmore, Chennai, Tamil Nadu, India International Ingredients & Excipients Pvt Ltd Full time**Job highlights** - Years of Experience: Minimum 5 Years in Medical Device/ Pharma/ Life science. Qualification: M Sc Life Science/ BTech Medical / B Pharm/ M Pharm. - Minimum of 2-3 years of experience in regulatory affairs Healthcare industry, with specific experience in USFDA / 510K submission and MDSAP Audit preparation **Job description** This is a...
-
Regulatory Affairs
2 weeks ago
Chennai, Tamil Nadu, India Ababil Healthcare Full timeRole - Regulatory Affairs - Medical Devices Experience - 1 to 3 Years Location- Madhavaram Chennai Budget - As per the industry Key Responsibilities 1 Regulatory Submissions Prepare and submit regulatory documents to authorities for approval such as new product applications amendments and supplements 2 Compliance Ensure products meet regulatory requirements...
-
Regulatory Affairs Executive
2 weeks ago
Tambaram, Chennai, Tamil Nadu, India Regenix Biosciences Ltd Full timeExperience: 0 to 1 years of experience in Regulatory affairs. Qualification: B. Pharm / M. Pharm / MSc. Biotechnology Description: Regulatory Affairs Handling Dossiers License Queries CFT Communication Life cycle etc. *Immediate Joiners* Excellent in Communication Application Question(s): - Current CTC - Expected CTC - Notice...
-
Regulatory Affairs Associate
4 days ago
Chennai, Tamil Nadu, India RegTrac Full time ₹ 9,00,000 - ₹ 12,00,000 per yearCompany OverviewRegTrac is a leading healthcare regulatory partner specializing in Global Regulatory Affairs, Quality Systems, and Compliance for Medical Devices, Cosmetics, and Consumer Products. With expertise in navigating regulatory requirements across diverse markets, RegTrac empowers MedTech companies to innovate and expand globally while ensuring...
-
Regulatory Affairs Executive
2 weeks ago
Chennai, Tamil Nadu, India LUMBAR HEALTHTECH PVT LTD Full time ₹ 1,92,000 - ₹ 2,64,000 per yearFull job descriptionThis role involves preparing, submitting, and managing regulatory documentation and applications to gain approval for products.Key Responsibilities:Prepare and submit regulatory applications to ensure timely approvals for new and existing products.Monitor and stay up-to-date on regulatory changes and requirements in different...
-
Regulatory Affairs Executive
2 weeks ago
Chennai, Tamil Nadu, India LUMBAR HEALTHTECH PVT LTD Full timeFull job description **Key Responsibilities**: - Monitor and stay up-to-date on regulatory changes and requirements in different regions. - Communicate with regulatory authorities and answer their queries or requests. - Ensure product labeling and packaging meet regulatory standards. - Maintain records of regulatory submissions, approvals, and...
-
Chennai, Tamil Nadu, India Morulaa Healthtech Full time ₹ 12,00,000 - ₹ 24,00,000 per yearJob Title: Senior Regulatory Affairs Team Lead Medical DevicesLocation: Chennai, IndiaDepartment: Regulatory AffairsExperience Required: Minimum 5 yearsReports To: Head of Regulatory Affairs / Director of Quality & RegulatoryJob Summary:We are seeking a highly skilled and experienced Senior Regulatory Affairs Team Lead to manage and lead our regulatory...
-
Regulatory Affairs Officer
1 week ago
T Nagar, Chennai, Tamil Nadu, India Sishya Meditech Pvt Ltd Full timeGeneral Accountability Responsible for regulatory affairs activities to assist in regulatory submission, annual reports, registrations and listings. Assure compliance with applicable medical device regulations per jurisdiction, guidance and standards. Assist in creation and maintenance of regulatory files. **Responsibilities**: 1. Write, analyze, and edit...