Regulatory Affairs Executive

Company 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...

Company 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...

Company 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...

We are in the process of hiring Regulatory Affairs **Job Title**: Regulatory Affairs Executive **Key Responsibilities**: **Qualifications**: Bachelor Degree in a related field such as Biomedical engineering, Mechanical engineering with minimum of 5 to 7 years’ progressive Regulatory affairs experience in medical device & quality...

We are in the process of hiring Regulatory Affairs **Job Title**: Regulatory Affairs Executive **Key Responsibilities**: **Qualifications**: Bachelor Degree in a related field such as Biomedical engineering, Mechanical engineering with minimum of 2 years’ progressive Regulatory affairs experience in medical device & quality...

**Job description** We are looking for a motivated and experienced Regulatory Affairs Specialist to join our team! As a Regulatory Affairs Specialist, you will be responsible for the day-to-day monitoring of the company’s regulatory activities to ensure compliance with all regulations. You will be a key member of our regulatory affairs team, which is...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. ClinChoice, is searching for an Executive - Regulatory Affairs (PLMDS) to join one of our clients. **Main Job Tasks and Responsibilities**: - Complete...

**Experience**: 1 to 2 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 **Job Types**: Full-time, Permanent Pay: Up to ₹28,000.00...

Job Summary The Regulatory Affairs Specialist is responsible for ensuring compliance with all applicable regulations governing the development, manufacturing, and distribution of the company's products. This role involves collaborating with internal teams and regulatory agencies to facilitate product registrations, approvals, and adherence to quality...

**Key Responsibilities**: - **Regulatory Compliance**: Ensure compliance with ISO 13485, EU MDR 2017/745, US-FDA, CDSCO, and other applicable international standards for medical devices. - **Submissions and Approvals**: Prepare, review, and submit regulatory documentation, including 510(k) and IMDR submissions, to regulatory authorities such as US-FDA,...

**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...

Job Title: Executive – Regulatory AffairsReporting to: Assistant Manager – Regulatory AffairsDivision: Ortho ImplantsLocation: ChennaiNo. of Positions: 1Education: B.E/ B. Tech in Biomedical Engineering / M. Pharm Regulatory AffairsExperience: 2 - 4 years Exp. in 'scientific writing / clinical documentation' role preferredKey Responsibilities:Technical...

Regulatory Affairs Specialist Job DescriptionAt Pfizer, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will play a key role in the preparation, publication, tracking, and quality control of our submissions to regulators in compliance with document management standards.Key...

Why Patients Need Regulatory Affairs Experts At Pfizer, we are committed to bringing medicines to the world faster and with excellence and integrity. A key part of this commitment is our Regulatory Affairs team, who work tirelessly to ensure that our products meet the highest standards of quality and safety. As a Regulatory Affairs Specialist, you will...

Why Patients Need YouPfizer is committed to bringing medicines to the world faster, without compromising on excellence and integrity. To achieve this, we need a dedicated team of regulatory experts who can navigate the complex regulatory landscape and ensure compliance with local and global regulations. As a Regulatory Affairs Specialist, you will play a...

Why Patients Need YouWe're committed to bringing medicines to the world faster, without compromising on excellence and integrity. To achieve this, we need dedicated professionals who can navigate the complex regulatory landscape. As a Regulatory Affairs Specialist at Pfizer, you will play a critical role in ensuring compliance with local and global...

Job Title: Regulatory Affairs SpecialistTTK Healthcare is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our Regulatory Affairs department, you will be responsible for ensuring compliance with regulatory requirements for our orthopedic implant products.Key Responsibilities:Technical writing, literature search,...

OverviewInternational Flavors & Fragrances is seeking a Regulatory Affairs Specialist to join our Global Regulatory Affairs team. As a key member of our team, you will be responsible for providing support to our regulatory and commercial colleagues to ensure a timely and accurate experience in regulatory and customer document...

Why Patients Need YouPfizer is committed to delivering innovative medicines and vaccines to patients worldwide. As a key member of our Regulatory Affairs team, you will play a critical role in ensuring the approval of our products in various markets. Your expertise in regulatory procedures, combined with your ability to communicate effectively with...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Pfizer. As a key member of our Regulatory Affairs department, you will be responsible for ensuring compliance with regulatory requirements and managing CMC change management processes.Key ResponsibilitiesPartner with internal and external partners to confirm...