Nectero Medical, Inc.’s Post

Hiring a Regulatory Manager should be completed in weeks not months. In our team, we complete most of our searches in less than 30 days for our clients. If you want to get a product to market and take 6 months to hire, you will be MASSIVELY behind schedule. Not forgetting the monetary value attached to the lost opportunities that commercialising your product could bring. Too many companies are obsessed with having several comparisons in a skill short market, missing out on talented applicants because they move too slowly. Customers that work with me, spend less time trying to hire and more time getting the product into new markets. Which means better revenue, better growth and not to mention better morale. DM me or email amy.holder@adecco.com to discuss how we can help you hire the right person quickly. #medicaldevice #medtech #regulatoryaffairs

Join the Quality Department as a Quality Associate Director of Regulatory Intelligence!  Apply now! The Quality Associate Director Regulatory Intelligence monitors the environment for regulatory compliance intelligence in the company's areas of interest to ensure that current awareness is maintained across the organization and, where necessary, that company procedures are introduced or adapted to respond to changes in the regulatory environment. #Quality #regulatory #regulation's #Director

𝗤𝘂𝗮𝗹𝗶𝘁𝘆, 𝗮 𝗴𝗿𝗼𝘄𝗶𝗻𝗴 𝗱𝗲𝗺𝗮𝗻𝗱. Quality is essential in the #lifescience industry. It’s quintessential to the safety, compliance, structure, and credibility of any business operating ! Therefore best talent in quality is in consistent demand, which can make finding the perfect candidate exceptionally tricky. That' why we're here to help. Our team is made up of life science experts with a passion for people. As market passionate professionals, we understand your industry needs better than average recruitment agencies. Our extensive international talent network allows us to identify and match the best quality professionals with the ideal opportunities. Our community network is consistently updated, and our connections are cherry picked to ensure that our clients benefit from the leading talent on the market. 𝗖𝗿𝘂𝗰𝗶𝗮𝗹 𝗶𝗺𝗽𝗮𝗰𝘁. Every aspect of the quality division contributes towards a safer and more efficient future in the life sciences. A comprehensive quality management function enables the innovation that meets tomorrow’s medical needs. For businesses in the life sciences, growth is much more than just making profit – it’s about bringing meaningful and positive change to the world as we know it, and quality is instilled at the heart of this transformation change. Adhering to the highest level of quality not only prevents life-threatening defects from occurring in a product or devices, but it streamlines processes for compliance and efficiency, boosting the bottom line. It’s a win-win when you find the right talent. Typical Roles and Responsibilities in 𝗧𝗲𝗰𝗵𝗢𝗽𝘀 𝗤𝘂𝗮𝗹𝗶𝘁𝘆: · QA/QC Engineers · Quality Manager / Director / VP · Quality Analyst/Officer · Quality Compliance/Vendor/Supply Chain · GMP/GxP/GDP expert · Lean Expert · Process Excellence Expert · Downstream/Upstream · Project Manager · Manufacturing / Production Engineers Let's discuss our unique approach to #talentattraction, that we successfully deployed to niche industries. Book a call for further insights : shorturl.at/aeCRX #hiring #biopharma #careergrowth

𝗤𝘂𝗮𝗹𝗶𝘁𝘆, 𝗮 𝗴𝗿𝗼𝘄𝗶𝗻𝗴 𝗱𝗲𝗺𝗮𝗻𝗱. Quality is essential in the #lifescience industry. It’s quintessential to the safety, compliance, structure, and credibility of any business operating ! Therefore best talent in quality is in consistent demand, which can make finding the perfect candidate exceptionally tricky. That' why we're here to help. Our team is made up of life science experts with a passion for people. As market passionate professionals, we understand your industry needs better than average recruitment agencies. Our extensive international talent network allows us to identify and match the best quality professionals with the ideal opportunities. Our community network is consistently updated, and our connections are cherry picked to ensure that our clients benefit from the leading talent on the market. 𝗖𝗿𝘂𝗰𝗶𝗮𝗹 𝗶𝗺𝗽𝗮𝗰𝘁. Every aspect of the quality division contributes towards a safer and more efficient future in the life sciences. A comprehensive quality management function enables the innovation that meets tomorrow’s medical needs. For businesses in the life sciences, growth is much more than just making profit – it’s about bringing meaningful and positive change to the world as we know it, and quality is instilled at the heart of this transformation change. Adhering to the highest level of quality not only prevents life-threatening defects from occurring in a product or devices, but it streamlines processes for compliance and efficiency, boosting the bottom line. It’s a win-win when you find the right talent. Typical Roles and Responsibilities in 𝗧𝗲𝗰𝗵𝗢𝗽𝘀 𝗤𝘂𝗮𝗹𝗶𝘁𝘆: · QA/QC Engineers · Quality Manager / Director / VP · Quality Analyst/Officer · Quality Compliance/Vendor/Supply Chain · GMP/GxP/GDP expert · Lean Expert · Process Excellence Expert · Downstream/Upstream · Project Manager · Manufacturing / Production Engineers Let's discuss our unique approach to #talentattraction, that we successfully deployed to niche industries. Book a call for further insights : shorturl.at/aeCRX #hiring #biopharma #careergrowth

𝗤𝘂𝗮𝗹𝗶𝘁𝘆, 𝗮 𝗴𝗿𝗼𝘄𝗶𝗻𝗴 𝗱𝗲𝗺𝗮𝗻𝗱. Quality is essential in the #lifescience industry. It’s quintessential to the safety, compliance, structure, and credibility of any business operating ! Therefore best talent in quality is in consistent demand, which can make finding the perfect candidate exceptionally tricky. That' why we're here to help. Our team is made up of life science experts with a passion for people. As market passionate professionals, we understand your industry needs better than average recruitment agencies. Our extensive international talent network allows us to identify and match the best quality professionals with the ideal opportunities. Our community network is consistently updated, and our connections are cherry picked to ensure that our clients benefit from the leading talent on the market. 𝗖𝗿𝘂𝗰𝗶𝗮𝗹 𝗶𝗺𝗽𝗮𝗰𝘁. Every aspect of the quality division contributes towards a safer and more efficient future in the life sciences. A comprehensive quality management function enables the innovation that meets tomorrow’s medical needs. For businesses in the life sciences, growth is much more than just making profit – it’s about bringing meaningful and positive change to the world as we know it, and quality is instilled at the heart of this transformation change. Adhering to the highest level of quality not only prevents life-threatening defects from occurring in a product or devices, but it streamlines processes for compliance and efficiency, boosting the bottom line. It’s a win-win when you find the right talent. Typical Roles and Responsibilities in 𝗧𝗲𝗰𝗵𝗢𝗽𝘀 𝗤𝘂𝗮𝗹𝗶𝘁𝘆: · QA/QC Engineers · Quality Manager / Director / VP · Quality Analyst/Officer · Quality Compliance/Vendor/Supply Chain · GMP/GxP/GDP expert · Lean Expert · Process Excellence Expert · Downstream/Upstream · Project Manager · Manufacturing / Production Engineers Let's discuss our unique approach to #talentattraction, that we successfully deployed to niche industries. Book a call for further insights : shorturl.at/aeCRX #hiring #biopharma #careergrowth

Hello #Connections We are hiring #MDR-Regulatory Affairs Specialist - Hybrid but open to remote for the right consultants. Note : Open only for W2 𝐓𝐨𝐩 3 𝐒𝐤𝐢𝐥𝐥𝐬 : Detail-oriented for review of product changes and documentation review, including labeling. Prior experience authoring EU MDR Technical documentation and managing review with notified body. Experience routing documents and changes through a controlled document control system. 𝐄𝐝𝐮𝐜𝐚𝐭𝐢𝐨𝐧 𝐑𝐞𝐪𝐮𝐢𝐫𝐞𝐝 : Bachelors in a scientific or technical discipline, engineering is preferred. Minimum of 3 years with advanced degree and Minimum of 5 years with a bachelor’s degree #eumdr #technicaldocumentation #labeling #documentation #regulatoryaffairs #controlsystem

🌟 Key Skills for Excelling in Continuous Improvement in the Med Device Industry 🌟 Achieving excellence in the medical device industry requires a strong focus on continuous improvement. Here are the three essential skills professionals need: Regulatory Compliance Expertise 📜 Master the intricacies of ISO 13485 and FDA regulations. Staying compliant with these standards ensures product reliability and safety, minimizing risks and maintaining market approval. Data-Driven Analysis 📊 Develop proficiency in tools like Six Sigma and Lean methodologies. Using data to drive decisions helps identify areas for improvement, optimize processes, and enhance overall efficiency. Effective Communication and Feedback Integration 🧠🗣️ Hone your ability to communicate effectively and integrate customer feedback. This ensures that improvements align with market demands and enhances customer satisfaction and loyalty. At Grove Technical Resources, we connect top talent with leading companies in the medical device industry. Follow us for the latest insights and opportunities! #MedicalDevices #ContinuousImprovement #QualityManagement #RegulatoryCompliance #MedTech #StaffingSolutions #FollowUs #Hiring #QualityEngineer #manufacturingengineer

💼 Are you looking to make a career change while staying in the familiar field of licensing and professional regulation? Your professional experiences and skillset in the regulatory sector can be easily transferred, opening up a wide range of employment opportunities that align with your goals. Discover the various opportunities available by visiting RegulatoryJobs.org. #professional #licensing #regulation #jobs #careers #change #consumerprotection #impact

#hiring Quality Assurance Specialist, Austin, United States, fulltime #jobs #jobseekers #careers #Austinjobs #Texasjobs #ScienceTechnology Apply: https://lnkd.in/gYxDRaXN Job Description Quality Assurance Specialist Job Description Maintain a safe, fast-paced, and positive laboratory environment. Interact directly with clients on an as-needed basis. Assist in training of other personnel as requested. Ensure safety and compliance with governmental regulations. Interact with FDA and clients as needed in the event of an inspection/audit. Follow all applicable Good Clinical Practice Regulations. Generally monitor studies to assure Management that the facilities, equipment, personnel, methods, practices, records, and controls are in conformance with Good Clinical Practice Standards. For any given study, be entirely separate from and independent of the personnel engaged in the direction and conduct of that study. Conduct inspections and maintain records or inspecting studies at adequate intervals and maintain written and properly signed records of each analytical/in-phase or periodic inspection. Report any problems which are likely to affect study integrity to the Principal Investigator and Management immediately. Maintain a copy of a master schedule of all studies, include all pertinent information. Maintain copies of all protocols pertaining to all studies for which the unit is responsible. Determine that no deviations from approved protocols or standard operating procedures were made without proper authorization and documentation. Review all Adverse Events and Serious Adverse Events reported. These are reviewed for accuracy, completion, and ensured to be communicated to the Study Sponsor and IRB

𝗤𝘂𝗮𝗹𝗶𝘁𝘆, 𝗮 𝗴𝗿𝗼𝘄𝗶𝗻𝗴 𝗱𝗲𝗺𝗮𝗻𝗱. Quality is essential in the #lifescience industry. It’s quintessential to the safety, compliance, structure, and credibility of any business operating ! Therefore best talent in quality is in consistent demand, which can make finding the perfect candidate exceptionally tricky. That' why we're here to help. Our team is made up of life science experts with a passion for people. As market passionate professionals, we understand your industry needs better than average recruitment agencies. Our extensive international talent network allows us to identify and match the best quality professionals with the ideal opportunities. Our community network is consistently updated, and our connections are cherry picked to ensure that our clients benefit from the leading talent on the market. 𝗖𝗿𝘂𝗰𝗶𝗮𝗹 𝗶𝗺𝗽𝗮𝗰𝘁. Every aspect of the quality division contributes towards a safer and more efficient future in the life sciences. A comprehensive quality management function enables the innovation that meets tomorrow’s medical needs. For businesses in the life sciences, growth is much more than just making profit – it’s about bringing meaningful and positive change to the world as we know it, and quality is instilled at the heart of this transformation change. Adhering to the highest level of quality not only prevents life-threatening defects from occurring in a product or devices, but it streamlines processes for compliance and efficiency, boosting the bottom line. It’s a win-win when you find the right talent. Typical Roles and Responsibilities in 𝗧𝗲𝗰𝗵𝗢𝗽𝘀 𝗤𝘂𝗮𝗹𝗶𝘁𝘆: · QA/QC Engineers · Quality Manager / Director / VP · Quality Analyst/Officer · Quality Compliance/Vendor/Supply Chain · GMP/GxP/GDP expert · Lean Expert · Process Excellence Expert · Downstream/Upstream · Project Manager · Manufacturing / Production Engineers Let's discuss our unique approach to #talentattraction, that we successfully deployed to niche industries. Book a call for further insights : shorturl.at/aeCRX #hiring #biopharma #careergrowth