We’re #hiring! CARGO is looking for a Director of Regulatory Affairs. Your work in this cross-functional role will support our mission to impact patients worldwide through the development of next-generation CAR T-cell therapies. You can read more about the role here: https://lnkd.in/eAzCw9vs #biotechjobs #careers
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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
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Medical Biological Scientist | Mail & Gaurdian Power of Women 2024 - STEMI Winner | Mentor | Co-Founder and Director, African Institute of Medical Scientists (AIMS) | Director of Chapters, Shadow A Scientist
Opportunity
Join us as a Technical Lead for Drug Development & Regulatory Processes! Lead market-shaping initiatives, work closely with CHAI, and drive impactful change in healthcare. Apply now: Vacancy24@wrhi.ac.za #JobOpening #TechnicalLead
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🚀 Awesome position alert 🚀 Oxford Nanopore Technologies is hiring a Senior Director of Regulatory Affairs, and I can't help but feel a little envious—wishing I had regulatory experience commensurate to this role: https://lnkd.in/gwPj53fD The upcoming launch of the Q-Line sequencing portfolio (kicking off with the GridION™ Q in 2025) represents the cusp of real-time, on-demand nanopore sequencing in a clinical-grade format, and it's poised to be the backbone for routine, long-term workflows in clinical and applied settings by mid-2025. 🌐 I see tremendous potential in the third generation of genome-sequencing technologies - in particular when built on a foundation that's ISO 9001:2015 compliant and adheres to 21 CFR Part 11 & EU GMP Annex 11 standards. OK, but *why* is this so exciting? It's not just the ability to bring epigenomics and epitranscriptomics into clinical practice, or to revolutionize pharmacogenomics ... Rather, as just one example, I'll offer this: there are good reasons to suspect that adaptive sequencing can streamline (clinical) genome-slicing protocols in ways that NGS-based assays cannot ... Finally, if none of that is exciting enough, the rapid evolution of the US and European regulatory landscapes promises a stimulating environment for those capable of navigating the intersection of technological innovation and regulatory frameworks. Can't wait to see who #ONT chooses for this role to maximize clinical impact! #Genomics #CareerOpportunity #RegulatoryAffairs #QLine #ISO9001 #ClinicalSequencing
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🚀 Wanted to outline some amazing Quality and Regulatory roles for my network!! 🚀 🌟 Regulatory Affairs Specialist - Medical Device 🌟 Quality Control Manager - Diagnostics 🌟 Regulatory Specialist - Medical Device/Mental Health 🌟 Quality Control Analyst - Diagnostics 🌟 Quality Engineer - Medical Device If you are on the look out for a new role or just want to discuss further feel free to pop me a message! #hiring #quality #regulatory #medicaldevice #iso13485 #pharmaceutical #qualitycontrol #qualityassurance #13485 #QMS #diagnostics
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How to get a regulatory affairs job? You should know the 3 basic things mentioned in the video. #job #career #pharmaceuticalindustry
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Pharmaceutical & Biologics - Head Hunter / Executive Search / Middle & Sr. Level Recruitment Specialist - 15000+
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
Pharmaceutical & Biologics - Head Hunter / Executive Search / Middle & Sr. Level Recruitment Specialist - 15000+
Dear Regulatory Affairs Professionals, Greetings!!! ***HIRING ALERT** Experience Level: 2 to 10 Years (CMC + US OR Canada) About Us: Biojobz is a global leading executive search and recruitment firm for the Pharma/Biotech sector. Biojobz Client Company: Global Pharmaceutical Company (German Healthcare group) (Global healthcare company that specializes in the production and supply of a wide range of pharmaceutical products and medical devices. They provide essential products and services that are crucial for patients and healthcare providers in various therapeutic areas, including critical care, anaesthesia, oncology, nutrition, and infusion therapy) Position: Regulatory Affairs Associate Job Location: Gurugram (North India) - Work from Office Employment Type: Full-time Number of openings: 20+ Experience Level: 2 to 7 Years (CMC + US OR Canada) CTC: Negotiable and depends upon experience and current CTC Responsibilities: -> Coordinate the necessary regulatory activities within the assigned scope to provide optimum support to all Business Units and Market Units for the end-to-end management of Variations and Renewals, including publishing and data management activities. -> Coordinate with the Production Units, API vendors, Qualified Persons etc. to obtain the documentation required for compiling the variation or renewal package in line with the prevailing guidelines of the regulatory agencies and the internal RA functions Coordinate with the Market Units for country-specific documents, proof of payments, letter of authorization, etc. -> Coordinate with Pharmacovigilance for PSUR, in case of renewals Compile the regulatory submission documentation in ICH CTO ACTD format, using the appropriate IT tools. Qualification and Work Experience: 1. Bachelor's degree in Life Science or related scientific field, Certificate in Regulatory Affairs beneficial. 2. Fluent in English (Written and spoken) 3. Qualification or certification in IT is advantageous. 4. Knowledge of the applicable guidelines on renewals, variations, eCTD, ICH guidelines etc. To apply, please submit your resume, and any relevant certifications to source@biojobz.com Or Call Snehal - 9011002940 for more details. Please Note: Your recommendations and references are highly appreciated and means lot to us. Regards, Ashok Salunkhe Biojobz | India #regulatory #regulatoryaffairs #usa #canada #ectd #pharmajobs #pharmahiring #cmc
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#regulatoryaffairs (RA) is a tough job by any measure, a pressure cooker of existing, new and ever-changing #pharmaceutical regulations, with tight deadlines for submissions, and wide-ranging responsibilities that, on any given day, may include updating databases, working on submission documents, reviewing #labelling and #packaging, rewriting #documentation, proofreading changes and much more. It may come as a surprise, but chance and a transfer within an organization – rather than a career choice from the outset – is how most regulatory affairs careers begin. Now-a-days the challenges for a Regulatory affairs #professional shift more and more to #strategic #planning and shaping the regulatory landscape. Pure filing, dossier compiling and publishing, submissions, team #management and hundreds of emails, all contribute to a never-ending daily grind! For more check the #workshops index link: https://lnkd.in/drtPxKcc #ra
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🔍 Opportunities in Quality Control 🔍 The demand for quality control professionals in biotech and pharmaceuticals is on the rise! As companies strive to meet rigorous regulatory standards and ensure the highest product quality, the role of QC teams is more critical than ever. At Viltis, we recognize the importance of maintaining excellence in quality, clinical, and regulatory areas. Whether you’re a seasoned QC expert or just starting your career, now is an exciting time to explore opportunities in this field. Check out this article from BioSpace highlighting 9 companies currently hiring for quality control positions: https://lnkd.in/gmJmMvpe As always, Viltis is here to support your journey in Quality, Clinical, Regulatory, Engineering, and Scientific areas. Let's work together to push the boundaries of what's possible in healthcare! #QualityControl #BiotechCareers #Viltis #HealthcareInnovation #QualityAssurance #RegulatoryAffairs
9 Companies Hiring Quality Control Jobs
biospace.com
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Hello LinkedIn friends! Is there anyone in my Med Device & Pharma network who may be interested (or have any recommendations for someone who may be) in some remote Regulatory consulting work? If so, please get in touch with me and I'll make an intro to my friend who's looking. #medicaldevices #regulatoryaffairs #fdacompliance #mdrcompliance #regulatorysubmissions #regulatory
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Vice President of Client Services & Recruiting at Gateway Recruiting - Life Sciences, Commerical Build Outs, Marketing| Now Accepting New Clients!
There's nothing quite like the satisfaction that comes from helping clients build successful teams. Teams that drive growth, innovation, and most importantly, better outcomes for patients. If your organization shares this same goal, let's connect to explore how we can partner to build a winning team together. #hiring #talentacquisition #sales #researchanddevelopment #marketing #legal #patientfocused #regulatory #engineering #clinicalresearch #medicaldevice #pharmaceteuicals #biotechnology
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