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Showing posts with the label REGULATORY AFFAIRS

"Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya"

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"Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya." (Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers) Introduction If you are a fresher or early-career professional aiming to build a strong career in Medical Device Regulatory Affairs and Quality Assurance , this opportunity can be a perfect starting point. ELEXES Medical Consulting Pvt. Ltd. has announced hiring for the position of Project Associate I – Regulatory Affairs & Quality Assurance (RA/QA) . This role is specially designed for fresh graduates and candidates with up to 6 months of experience who want hands-on exposure to global medical device regulations , including US FDA, EU MDR, CDSCO, Health Canada , along with ISO 13485 quality systems . The position offers real project experience under expert mentorship, making it ideal for long-term growth in the medical device regulatory domain. About The Company – ELEXES Medical Consulting Pvt. Ltd. EL...

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"Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya"

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"Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya." (Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers) Introduction If you are a fresher or early-career professional aiming to build a strong career in Medical Device Regulatory Affairs and Quality Assurance , this opportunity can be a perfect starting point. ELEXES Medical Consulting Pvt. Ltd. has announced hiring for the position of Project Associate I – Regulatory Affairs & Quality Assurance (RA/QA) . This role is specially designed for fresh graduates and candidates with up to 6 months of experience who want hands-on exposure to global medical device regulations , including US FDA, EU MDR, CDSCO, Health Canada , along with ISO 13485 quality systems . The position offers real project experience under expert mentorship, making it ideal for long-term growth in the medical device regulatory domain. About The Company – ELEXES Medical Consulting Pvt. Ltd. EL...

"Regulatory Affairs Officer Job in Ahmedabad | Advin Health Care Hiring Freshers | Pharma Duniya"

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"Regulatory Affairs Officer Job in Ahmedabad | Advin Health Care Hiring Freshers | Pharma Duniya" (Regulatory Affairs Officer Job in Ahmedabad) Introduction If you are a fresher or early-career professional looking to start a long-term career in Medical Device Regulatory Affairs , then this opportunity can be a strong foundation for your future. Advin Health Care , a growing name in the medical device manufacturing sector, has opened recruitment for the post of Regulatory Affairs Officer at its Ahmedabad facility . This role is especially suitable for freshers (0–1 year experience) who want hands-on exposure to CDSCO submissions, Medical Device Rules (MDR), 2017, ISO 13485 Quality Management System , and global regulatory frameworks such as US FDA and EU MDR . About The Company – Advin Health Care Advin Health Care is an Indian medical device manufacturing and regulatory-driven organization focused on delivering high-quality, compliant, and innovative medical devices...

"Good Manufacturing Practice (GMP) in Pharmaceuticals: Meaning, Principles, Importance and Real-Life Examples"

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"Good Manufacturing Practice (GMP) in Pharmaceuticals" (Good Manufacturing Practice (GMP) in Pharmaceuticals) Good Manufacturing Practice (GMP) is a quality system that ensures pharmaceutical products are consistently manufactured and controlled in accordance with established quality standards. GMP plays a critical role in protecting patient safety by minimizing risks such as contamination, mix-ups, and manufacturing errors. In the pharmaceutical industry, GMP is not optional. It is a legal and regulatory requirement enforced by authorities such as the WHO, the FDA, the EMA, and the CDSCO to ensure that medicines are safe, effective, and of high quality. What is GMP? Good Manufacturing Practice (GMP) refers to a set of guidelines and regulations that govern the manufacturing, processing, packaging, labeling, storage, and distribution of pharmaceutical products. GMP ensures that: Products are produced consistently Quality is built into the process Finished medici...

"HR Interview Questions in Pharma Industry | Pharma Jobs HR Round Preparation Guide"

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"HR Interview Questions in Pharma Industry | Pharma Jobs HR Round Preparation Guide" (HR Interview Questions in Pharma Industry | Complete Guide) Introduction Cracking an HR interview in the pharmaceutical industry is just as important as clearing technical rounds. Many candidates fail not because of a lack of technical knowledge, but due to poor HR interview performance. The HR round in pharma companies focuses on your attitude, communication skills, stability, ethics, and long-term career goals. Whether you are a pharma fresher or an experienced professional , preparing common HR interview questions in the pharma industry can significantly increase your chances of selection. This article provides a complete HR interview preparation guide for pharma jobs , including commonly asked questions, sample answers, and expert tips. About the Pharma HR Interview Process Pharmaceutical companies follow strict compliance, ethics, and quality systems. HR departments evaluate wh...

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