Regulatory Affairs Jobs in Life Sciences’ Post

Embarking on a career in regulatory affairs within the pharmaceutical industry presents unique challenges and immense opportunities. At United Pharma Tech, we specialize in guiding professionals like you through the complexities of this vital field. 📜 Expert Insight into Regulatory Landscapes: The world of regulatory affairs is intricate, constantly evolving with new laws and guidelines. Our expertise at United Pharma Tech offers you a deep dive into these changes, equipping you with the knowledge to excel. 💼 Targeted Career Opportunities in Regulatory Affairs: We understand the nuances of regulatory roles – from compliance officers to policy advisors. Our focus is to connect you with positions that not only match your skill set but also align with your career aspirations in regulatory affairs. 🌏 Expansive Network, Focused Results: Our extensive connections in the pharma industry open up opportunities both globally and locally, offering you a wide array of career paths in regulatory affairs. 📚 Continual Learning and Development: In a field where staying updated is key, United Pharma Tech provides resources and support for continuous learning and skill development, ensuring you remain at the forefront of regulatory expertise. 👥 Personalized Career Guidance: Our dedicated team takes the time to understand your career goals, providing personalized guidance and support tailored to the specific demands and opportunities in regulatory affairs. As you look to make your mark in ensuring the safety, efficacy, and compliance of pharmaceutical products, United Pharma Tech is here to support your journey every step of the way. Let’s connect and discover how we can help launch or advance your career in regulatory affairs. #UnitedPharmaTech #RegulatoryAffairs #PharmaCareers #CareerDevelopment

Opportunity

Dear All, 🚀 Ready to dive into regulatory affairs? It's a path filled with rewarding challenges and opportunities. Here's a breakdown of this field: 🔍 Understanding Regulatory Affairs: In life sciences, regulatory affairs ensures the safe development of healthcare products. Think pharmaceuticals and medical devices. 🤓 Role of a Regulatory Affairs Pro: They keep up with evolving laws, offer compliance guidance, and organize vital data. They prepare registration docs and handle market authorizations, even approving packaging and ads. 💥 In-Demand Career: Industries like pharmaceuticals and medical devices are always on the lookout for skilled regulatory professionals. Exciting opportunities await! 🌟 Your Path in Regulatory Affairs: Whether you're dreaming of entering this field or are a seasoned pro seeking new challenges, let's chat! Share your thoughts or questions below. #RegulatoryAffairs #RAjob #howtogetaRAjob #CareerAdvice #LifeSciences 📊🏥💼

🔍 Exploring New Frontiers in Pharma! 🌐 Today, on Rare Diseases Day, we celebrate the resilience of individuals facing uncommon health challenges. I am thrilled to be part of a mission-driven journey in finding exceptional talent for a Regulatory Affairs Director position at a leading rare disease company based in the USA. 🌟 This role is not just a career move; it's an opportunity to contribute to groundbreaking advancements in healthcare. As we raise awareness about rare diseases, let's also recognize the impact regulatory affairs professionals can have in ensuring these life-changing therapies reach those who need them most. 🧬 If you are a Regulatory Affairs Director passionate about navigating the complex regulatory landscape and dedicated to bringing innovative therapies to market, I want to hear from you! Let's connect and discuss how your expertise can make a significant impact in the world of rare diseases. 👥 Tag someone you think might be interested or share this post to spread the word! Together, let's make a difference in the lives of those affected by rare diseases. #RareDiseasesDay #PharmaRecruitment #RegulatoryAffairs #HealthcareInnovation #JoinTheMission 🌍💙

hello #connection #recruiters , I actively looking for job opportunities in drug and medical devices field , so if you have any opportunity please let me know. I have experience in Regulatory affairs and medical devices. others experience you can find through my profile. #mankindpharm #medicaldevices #cipla #fortishealthcare #ipc #drugdevelopment #pharmacovigilance #jhonsonandjhonson #simens #unilever #gehealthcare #regulatorycompliance #fdacompliance #medicalaffairs

Promising career prospects await regulatory affairs professionals. Apply now! #regulatorysubmissions #regulatorycompliance #regulatory #regulatoryaffairs #cmc #ectd #ctd #pharmajobs #pharmacyjobs #biotechjobs #indiajobs #delhijobs #gurugramjobs #gurugramrealestate #gurugramcity -#northindia #pharmaprofessionals #regulatorylaw #regulatoryrequirements #regulatoryapproval

Introducing VED Consulting – your trusted partner for executive search services in clinical and regulatory affairs. At VED, we are driven by a passion for bringing innovative and cost-effective treatments to patients around the world. Our team of seasoned experts has decades of experience in clinical and regulatory affairs for drug development. We understand the critical role that top-tier talent plays in achieving success. Our personalized approach to executive search sets us apart from the competition. We work closely with you to understand your unique business needs and develop customized solutions that meet your specific requirements. With a deep understanding of the clinical and regulatory affairs space, we are able to identify and bring in the best candidates for your organization. At VED, we utilize the latest technologies and innovative strategies to find and attract top-tier talent from around the world. Our extensive network of industry contacts, combined with our expertise in the clinical and regulatory affairs domains, ensures that we are able to identify the right candidates to lead your organization to success. Partnering with VED Consulting means working with a team of seasoned professionals who have been in your shoes. We know what it takes to drive drug development and bring innovative treatments to patients, and we're committed to helping you find the right talent to achieve your goals. Visit www.thevedconsulting.com today to learn more about our executive search services in clinical and regulatory affairs. Let us help you find the right talent to take your business to the next level. #ExecutiveSearch #regulatoryaffairs #regulatorystrategy #Clinical #clinicalresearch #talentacquisition #drugdevelopment #globaldevelopment

Career dreams evolve, and that's perfectly FINE. As an industry resident, my friend and co-resident and I used to dream of ascending the corporate ranks to become Directors of Regulatory Affairs. We would pretend we were one person in particular! Both of us ended up taking VERY different paths. We aren't done yet. Share in the comments what you THOUGHT you wanted to do and what you NOW want to do. #careerdevelopment #careers #pharma #growthmindset #embracechange #jobseeker

****HIRING**** Site Readiness and Regulatory Operations Specialist Job Description • Develop awareness of regulatory legislation, guidance and practice in the assigned countries with the support from senior staff • Assist senior staff to compile, prepare, submit and obtain approval of the submission documents to IRB/IEC/Third body/Regulatory Authority in accordance with local requirements • Liaise with internal and external vendors in the generation of Regulatory Authority submissions (as applicable) • Perform a review of final submission documents as applicable ¨ Organize communication related to the submissions/outcomes within Labcorp as applicable ¨ Escalate study issues appropriately and in a timely fashion • Perform other duties as assigned by management depending upon country and situational requirements with proper supervision (if applicable) In Country specific tasks (Global) • Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner • Collect and track all the necessary documents required and perform a quality review, formatting and compilation of the final documents for effective and compliant site activation and maintenance • Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines • Update study documents when there are changes in study personnel/study amendments • Ensure high quality documents are filed and systems are updated on an ongoing and timely basis making Labcorp ready for an audit at any time • Update status reports, applicable logs and tracking systems as applicable for the projects with input provided by senior staff • With guidance from line manager and experienced colleagues, adapt Informed Consent Forms and other patient facing material to country specific requirements: • May support / assist the contract negotiation process under supervision of an experienced colleague or line manager • Proactively identifying and escalating to Submission Leads any risk to meeting deliverables • Notify the Submissions Lead of hours identified as Out-of-Scope or over burn with the support of more senior specialists Additional Skills & Qualifications Experience: Minimum 1 - 2 years of experience, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job • Working knowledge of ICH, RA, IRB/IEC and other applicable regulations/guidelines. Demonstrated basic understanding of the clinical trial process