Eslam Elgebaly’s Post

Completing My Internship Journey! I'm thrilled to announce that I've successfully completed my 1st internship program at [Pharmaceutical Company ]! 💎Gained hands-on experience in [specific areas, e.g., research, quality control, regulatory affairs] 💎Developed valuable skills in [e.g., data analysis, teamwork, communication] 💎Contributed to [projects/initiatives] that impacted [specific outcomes] 💎Networked with professionals in the pharmaceutical industry 💎Enhanced understanding of [industry-specific knowledge] 💥Grateful for: 💎Mentorship from experienced professionals 💎Opportunities for growth and learning 💎Collaborative team environment 💎 Applying knowledge and skills in future endeavors 💎Pursuing a career in the pharmaceutical industry 💎Continuing to learn and innovate *Thank you* [Pharmaceutical Company Name] for the invaluable experience! #PharmaceuticalInternship #CareerGrowth #ProfessionalDevelopment #LinkedIn

How do you start your career in Regulatory Affairs? Gaining experience in regulatory affairs can be a challenging task. Many regulatory affairs jobs require candidates to have prior experience, and even entry-level positions can require up to 2 years of related experience. However, there are several ways to gain the experience you need to break into this field. One of the best ways is to take an internship. Many companies offer internships to science graduates and these placements can be a great way to gain regulatory experience and network with the industry. Many universities offer 1 year placements too, which allow you to take a year off from their studies to gain work experience. It can prove to be a significant advantage when you do eventually look to begin your career. You can also start in a related field and work your way into regulatory affairs. For example, many RA professionals started their careers working in formulation, product development, or other roles where they could develop technical expertise of the drug development process. This can be a good way to gain experience of regulatory frameworks and improve your technical understanding. If you are a registered pharmacist, you can also gain regulatory experience working as a pharmaceutical assessor for the FDA, MHRA, EMA, or equivalent national competent authority in your country. This can be a great way to gain experience and can serve as valued experience to prospective employers. Regulatory-specific qualifications on your CV is also a great way to stand out. Many organizations, such as TOPRA, offer well-recognized entry-level courses that can help you gain the knowledge and skills you need to succeed in regulatory affairs. It will be tough, but once your foot is in the door, you can expect a really exciting future for your career. #regulatoryaffairs #lifesciences #lifesciencesjobs #biotech #pharma

Reflecting on My Internship Experience at Khandelwal Laboratories Last year from June 1, 2023, to June 30, 2023, I had the incredible opportunity to intern at Khandelwal Laboratories. Even though it’s been a while, I want to share my experiences and the valuable insights I gained during my time there. During my one-month internship, I focused on anticancer formulations and the quality assurance and quality control aspects of these crucial treatments. This experience allowed me to: - Gain a deep understanding of the development process of anticancer drugs. - Enhance my skills in quality assurance practices to ensure the efficacy and safety of pharmaceutical products. - Learn the intricacies of quality control testing and regulatory compliance. #Internship #ProfessionalGrowth #LearningExperience #PharmaceuticalIndustry #QualityAssurance #QualityControl #AnticancerFormulations

Any of you interested in joining Pharmacovigilance in Work from home mode? There are openings in the Pharmacovigilance , especially for pharma and life science candidates in work from home mode . Guys stay tuned with THE DRUG INDEX for the notification. Interested candidates are requested to send a direct message (DM) to me through LinkedIn inbox(kindly mention preferred domain and location), Despite receiving a lot of requests in my inbox, I will do my best effort to send you the details via message. If you haven't received them, don't worry. Just keep an eye on my Linkedin feed for updates and links to apply through company websites or HR details. Connect Aman Kumar Subudhi to Know more. Join THE DRUG INDEX groups ⏩ https://lnkd.in/g6NZb-Hb Disclaimer: We're not affiliated with the company. At Mission Helping Hands, we gather and distribute internship/job opportunities from company websites for students. This service is free. Information is shared in good faith. We don't influence candidate selection.

Dear All, We are pleased to announce the commencement of our online/offline training courses for Pharmacovigilance (PV) aspirants, catering to two distinct categories: 1. Job Oriented Training & Certification Course in Pharmacovigilance (PV) Course Overview * Duration: 2 months * Start date: 02 Apr 2024 * End date: 31 May 2024 * Timing: 10:00 AM to 06:00 PM, Monday to Friday Key Features: ✓ Comprehensive Placement Assistance: Receive dedicated support for placements in Pharmacovigilance, Clinical Research, and related fields. ✓ Expert-led Training: Benefit from sessions by industry professionals and corporate trainers. ✓ Aptitude Test and Technical Round Preparation: Equip yourself with the skills necessary to excel in aptitude tests and technical interviews. ✓ Tailored Study Materials: Access high-quality study materials curated for Pharmacovigilance. ✓ Direct Interaction with Industry Experts: Engage in valuable interactions with industry leaders to sharpen your interview preparation. ✓ Certification of Accomplishment: Earn a recognized certification upon successful completion of the course. 2. Training and Certification Course in Pharmacovigilance (PV) followed by 10 month contract employment Course Overview * Duration: 12 months * Start date: 02 Apr 2024 * End date: 01 Apr 2025 * Timing: 10:00 AM to 06:00 PM, Monday to Friday Key Features: ✓ Rigorous 2-Month Training: Led by seasoned industry experts and corporate trainers, ensuring comprehensive skill development. ✓ Aptitude Test and Technical Interview Preparation: Equip students with the necessary tools to excel in assessments and technical interviews. ✓ Curated Study Material: Access to meticulously curated study resources tailored to enhance learning outcomes. ✓ Direct Interaction with Industry Leaders: Gain invaluable insights and guidance through direct interactions with industry experts, enhancing interview preparedness. ✓ Post-contract Placement Assistance: Dedicated support for securing placements in Pharmacovigilance, Clinical Research, and related fields after the internship. ✓ Experience Letter: Receive an official experience letter upon successful completion of the internship, bolstering your professional credentials. For further details, contact us at +91-9420352357. #Pharmacovigilance #Training #ContractEmployment #PV #Placement

🎉 I'm excited to share that I recently completed a two months course on pharmacovigilance from Skill Dunia (ISO 2009:2015 Certified) associated with Odcet Technologies. In this course I covered wide range of topics: • Introduction to pharmacovigilance. • History and evaluation of Pharmacovigilance. • Drug discovery and development. • Terminologies in pharmacovigilance. • Types of adverse events. • Pharmacovigilance global guidelines. • Sources of adverse events. • Criteria for reporting. • Seriousness and labelling assessment. • Regulatory expedited reporting requirements and timeline. • Medical dictionary for regulatory activities (MedDRA). • Casualty assessment. • Narrative writing. • Case follow up , pharmacovigilance audits and inspection. • Vaccine vigilance and materiovigilance. • Database used in pharmacovigilance. Along with this course I also had the opportunity to do a project based on pharmacovigilance. Thanks to Skill Dunia (ISO 2009:2015 Certified) . #Pharmacovigilance #Development #Internship #DrugDiscovery #DrugDevelopment

"Excited to share that I have successfully completed my internship at Cipla Ltd, Bengaluru, in the ADL (Analytical Development Lab) department & Quality control department! During this enriching experience, I had the opportunity to enhance my skills in instrument handling and gained in-depth exposure to various analytical techniques. A big thanks to the amazing team and mentors at Cipla who supported and guided me throughout this journey. Looking forward to apply the knowledge and skills gained to future opportunities in the pharmaceutical industry! #Internship #Cipla #Pharmaceuticals #ADL #QC #InstrumentHandling #CareerGrowth"

"Excited to share that I have successfully completed my internship in the pharmaceutical industry! 🎉 It has been an incredible learning experience, where I had the opportunity to work on various projects and gain valuable insights into the industry. I want to express my gratitude to [Scilife Pharma (Pvt.) Limited for providing me with this opportunity. Looking forward to applying the knowledge and skills I've acquired in my future endeavors. #InternshipExperience #PharmaceuticalIndustry #LearningAndGrowth"