| Job alert | Jobs 1 - 10 of 22 |
SENIOR QA/RA EXECUTIVE
GPC Medical Ltd.
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India Gate, Delhi, 110011, India
... Roles and Responsibilities · Proficient in drafting and evaluating documents in accordance with ISO 13485, EU-MDR, 21CFR820, Thai FDA, and Indian Medical Device Regulations, ensuring their effective implementation. • Compile regulatory documents ... - Apr 30
Analyst - Engineering
Ual-Pro
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Sector 25, Haryana, 122015, India
... This includes duties for Engineering Data Input (EDI), the ODA STC, the PMA ODA and the FDA. Support Engineering Data Input (EDI): Accountable for entries into SCEPTRE system. Reviewing, creating and attaching records tracking numbers, parts, ... - Apr 02
Color Cosmetic Production Manager
BEYOBO
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Delhi, India
... Knowledge of regulatory requirements for cosmetic manufacturing (FDA, ISO, etc.). Strong commitment to safety, quality, and environmental sustainability. Join our dynamic team and contribute to the creation of innovative and high-quality color ... - Apr 26
Regulatory Affairs Executive(Male)
Zeon Lifesciences Ltd
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Noida, Uttar Pradesh, India
... Our certifications include FSSAI, AYUSH GMP, NSF USA-GMP, FDA, and WHO GMP. Role Description: Roles and Responsibilities: Studying scientific and legal documents Gathering, evaluating, organizing, managing and collating information in a variety of ... - Apr 07
Sr. Design Assurance Quality Engineer
hollister.com
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Gurugram, Haryana, India
... Working knowledge of ISO 13485 and FDA 21 CFR Regulations and BS EN ISO 14971 Software: Knowledge and experience of Word, Excel, PowerPoint and Minitab Knowledge of statistical data analysis An ability to work independently and as part of a team. ... - Apr 05
Remote Informatica Developer (Pharmaceutical)
Pharma Companies
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Noida, Uttar Pradesh, India
4-7 Lacs P.A.
... Compliance: Ensure that all data integration solutions adhere to industry regulations, especially within the pharmaceutical sector, such as HIPAA and FDA guidelines. Documentation: Create and maintain comprehensive documentation for all ETL ... - Apr 09
Manager, Compliance Auditing and Monitoring, High Growth Markets
Danaher
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Delhi, India
... of Medical Device and Diagnostics operations and the laws, regulations, and guidance applicable to the industry (e.g., FDA/CDSCO, MedTech, and other international industry codes, global transparency laws, Anti-Bribery/Anti-Corruption, Data ... - Apr 21
Senior Manager Regulatory Affairs - Agrochemical
Om Sai Global HR Service
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Sector 56, Haryana, 122003, India
... with regulatory authorities Provide regulatory input and support to product development teams Ensure compliance with FDA regulations and other relevant regulatory standards Manage relationships with regulatory agencies and keep abreast of ... - Apr 26
PMS-Complaint handling
ALTEN
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Gurugram, Haryana, India
... Understanding of Post Market Surveillance requirement of Medical Devices under FDA & EU MDR regulations Understanding on Medical Device Risk Management Hands-on Experience on Complaint handling and Product investigations of medical devices. ... - Apr 18
QA Manager (medical devices manufacturing))
Desire Consultancy Services
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Delhi, India
... medical devices manufacturing industry Expert knowledge of quality management systems and regulatory requirements (ISO 13485, FDA regulations) Strong leadership and managerial skills Excellent problem-solving and decision-making abilities Effective ... - Apr 26