Exciting Opportunity in Sligo! 📍 Are you a quality-driven professional looking for your next challenge? Our global healthcare client based in Sligo is on the lookout for a talented Quality Manufacturing Supervisor. This role is pivotal in ensuring the highest standards are maintained in our product manufacturing, reflecting our commitment to excellence and innovation. In this position, you'll be overseeing the manufacturing processes, ensuring compliance with industry standards, and driving continuous improvement. Your insights and expertise will play a crucial role in helping us deliver top-notch healthcare solutions that make a real difference in people's lives. If you have a keen eye for detail and a passion for quality, we want to hear from you! Join us and be part of a dynamic team where every day is a chance to innovate, improve, and impact the global healthcare landscape. Are you ready to make a significant difference? Drop us a comment or like if this sounds like the opportunity you've been waiting for! 🚀 #HealthcareJobs #QualityAssurance #SligoOpportunity
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Are you interested in a career in #regulatoryaffairs? Take a look at our latest article, where we've outlined 10 of the top skills typically needed to succeed in this field: https://buff.ly/3UMwP6g. #regaffairs #skilldevelopment #jobsearch #nichejobboard #lifesciencejobs
Top 10 Skills Required for Careers in Regulatory Affairs
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Are you interested in a career in #regulatoryaffairs? Take a look at our latest article, where we've outlined 10 of the top skills typically needed to succeed in this field: https://buff.ly/3UMwP6g. #regaffairs #skilldevelopment #jobsearch #nichejobboard #lifesciencejobs
Top 10 Skills Required for Careers in Regulatory Affairs
pharmiweb.jobs
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Are you interested in a career in #regulatoryaffairs? Take a look at our latest article, where we've outlined 10 of the top skills typically needed to succeed in this field: https://buff.ly/3UMwP6g. #regaffairs #skilldevelopment #jobsearch #nichejobboard #lifesciencejobs
Top 10 Skills Required for Careers in Regulatory Affairs
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Are you interested in a career in #regulatoryaffairs? Take a look at our latest article, where we've outlined 10 of the top skills typically needed to succeed in this field: https://buff.ly/3UMwP6g. #regaffairs #skilldevelopment #jobsearch #nichejobboard #lifesciencejobs
Top 10 Skills Required for Careers in Regulatory Affairs
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Cracking Ireland's growing life sciences sector? 🌱 If you've got an eye for detail and a passion for excellence, this might just be your moment. Within the bustling world of pharma and biotech, with over 50 FDA-approved plants right here in Ireland, there's a burgeoning demand for Quality Assurance (QA) mavens. As your go-to recruiter at Hyper Recruitment Solutions, I've been on the frontline, witnessing the demand for top-tier QA professionals. They're the unsung heroes ensuring our local innovators reach the pinnacle of world-class standards. The role of QA in our industry can't be overstated: it's all about driving breakthroughs while securing the high-calibre reputation of Ireland's pharmaceutical landscape. Akin to the immune system in our bodies, QA pros are the vital defence, guaranteeing our products can be trusted worldwide. So, fancy a career leap? If you're ready to play a key part in this exhilarating narrative, I'm merely a message away. Together, we can explore the wealth of opportunities awaiting you in this dynamic field. Reach out, let's talk Quality Assurance, and make your mark in securing the future of healthcare. 🌟 #QualityAssurance #LifeSciences #HRS
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Are you interested in a career in #regulatoryaffairs? Take a look at our latest article, where we've outlined 10 of the top skills typically needed to succeed in this field: https://phrmwb.com/44wzp3o. #regaffairs #skilldevelopment #jobsearch #nichejobboard #lifesciencejobs
Top 10 Skills Required for Careers in Regulatory Affairs
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Quality Assurance-PMS | Regulatory Affairs | EU MDR | Power BI, TrackWise, SAP| ISO-13485 | 21 CFR Part 820 | Medical device QA/RA |Risk Management | CSV | SLR, Evidence Synthesis, Meta Analysis, HTA
Hello LinkedIn Family! 🌟 Wishing you all a fantastic time as we dive into year-end tasks and extend early Christmas cheer!🎄 For those who've known me from my Pharmacy days and professional journey, your support has been invaluable. As we navigate both professional and personal growth, the pursuit of potential and self-motivation remains key. Recently, I've noticed a limited number of openings in the medical devices complaint handling division. Are any of you facing similar challenges in finding opportunities? I want to bring your attention to a transition I am exploring for professional growth. As a Medical Device Safety Officer, I bring substantial experience in: Complaints Investigator: Conducting thorough investigations, preparing technical summaries for product failures, and collaborating across teams. Analyzing data, drafting MedWatch reports for FDA submission, and contributing to trending analyses for continuous improvement. Complaints Evaluator: Evaluating medical device data, identifying and adding failure or defect allegations. Determining if failures represent adverse events/reportable defects and escalating to the FDA when necessary. Global Complaint Handling.Managing the global complaint handling process, evaluating customer feedback, and interacting with stakeholders for comprehensive data gathering. I'm on the lookout for new opportunities, and your references, job leads, or insights into skill-up programs would be greatly appreciated. Let's connect and explore the possibilities together! 🚀 #CareerTransition #MedicalDevices #ProfessionalGrowth #drugsafety #medicaldevices #regulatoryaffairs
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Are you interested in a career in #regulatoryaffairs? Take a look at our latest article, where we've outlined 10 of the top skills typically needed to succeed in this field: https://phrmwb.com/4b70GMe. #regaffairs #skilldevelopment #jobsearch #nichejobboard #lifesciencejobs
Top 10 Skills Required for Careers in Regulatory Affairs
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I Help Medical Device Companies master the MDR in Europe | MedTech Entrepreneur | Regulatory Affairs Expert | Innovator in Global Health | Founder & CEO | Empowering Health Through Technology | Passionate about MedTech
🌟 "Being a regulatory expert is just about hard skills!" While holding the role of a regulatory affairs manager is well-respected, some may find it a bit peculiar. Regulatory experts may seem to hide behind rules, setting guidelines for marketing and sales, and always asking for data from all corners of the company. I had a similar experience early in my career. When I led my first startup, my initial regulatory responses to various aspects of development and market entry often leaned towards, 'We can't do that because...!' After some time, it might happen that team members and colleagues will start to dislike regulatory affairs and even the people trying to comply with the regulations. The good news is that a strong set of soft skills can work wonders, not only for the regulatory expert but for the whole team and company. Here are 5 soft skills I highly recommend adopting: 1️⃣ Communication Skills 🗣️ Recognize that how you talk to a software developer is different from how you talk to someone from marketing or sales. Understand their perspectives, needs, and how they communicate, and adjust accordingly. 2️⃣ Problem-Solving 🧩 No medical device project goes without challenges. You'll play a critical role in solving problems, often requiring creative solutions. Instead of just saying no to ideas, explain the regulatory context and propose alternative solutions. 3️⃣ Attention to Detail 🔍 Regulatory experts must be careful because even small mistakes can lead to extra work during certification. Nobody's perfect, but often, double-checking is a good idea. 4️⃣ Project Management 📊 You'll become a project manager, whether it's officially in your job description or not. You'll need to coordinate development, manufacturing, and post-market surveillance. Becoming a good project manager takes time and experience. 5️⃣ Adaptability 🌐 Not only does the regulatory landscape change, but a company's goals, priorities, and even team members may shift. Being flexible and adaptable isn't just helpful; it can reduce a lot of stress. None of these skills can be mastered overnight. The key is consistent improvement, learning from mistakes, and gaining experience. A truly outstanding regulatory affairs expert possesses a blend of hard and soft skills. While experience is crucial, having the right skill set can kick-start any career. What soft skills did you prioritize at the beginning of your regulatory career, and what challenges did you face? #MDR #MedicalDevices #RegulatoryAffairs #MedicalDevice #EUMDR
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Meet Ashley O'Banion, Senior Quality Assurance Specialist with Consilium for 1 year and 9 months. In your opinion, what sets Consilium apart from others in our industry? Consilium genuinely cares about its team members. I have never worked for a company that cares so much for the growth and well-being of their staff. You would not believe the breath of fresh air I received the moment I stepped foot in these doors my first day. How do you define success? Success is not the key to happiness. Happiness is the key to success. If you love what you are doing, you will be successful! What’s the first concert you ever attended? Tom Petty and the Heartbreakers! #consilium #morethanplacements #bestinstaffing #youareconsilium#newcareer #recruitingjobs #DMNTop100 #healthcarestaffing #locums #locumtenens #physician #locum #locumlife #healthcare #doctor #md #healthcaretraveler #locumjobs #doctorsofinstagram #travelingdoctor #traveldoctor #healthcareprofessionals #doctors #recruitment #locumwork #tribalhealth #doctorjobs #medicaljobs #medicalcareer #teamspotlight
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