GxP Recruitment’s Post

🔍 Looking for contracting support for your Medical Affairs or Regulatory teams?   With expertise across various projects and therapeutic areas, contractors are equipped to deliver results from day one. 💡 Why should you consider hiring a contractor for your team? 💲 Contractors can offer cost-effective solutions as they are often hired for specific projects or periods, reducing long-term overhead costs. 🔒 Contractors bring specialized skills that may not be available in-house, allowing teams to tackle complex tasks or projects efficiently. ⚖ Teams can easily scale up or down by leveraging contractors, adapting to workload fluctuations or project demands without the need for permanent hires. 👇Reduced Training Time - contractors have industry experience, requiring minimal training and allowing teams to achieve quicker project turnaround times. 👀Fresh Perspectives: Contractors bring fresh ideas and perspectives from their varied experiences, contributing to innovative problem-solving and decision-making within the team.   Stay ahead by leveraging this versatile talent pool for your short or medium-term requirements. Lets chat - 02 8877 8776! #medicalaffairs #regulatoryaffairs #contracting

TOP CONTRACTOR THURSDAY Looking for contracting support for your Medical Affairs or Regulatory teams? With expertise across various projects and therapeutic areas, contractors are equipped to deliver results from day one. 💡 Why should you consider hiring a contractor for your team? 💲 Contractors can offer cost-effective solutions as they are often hired for specific projects or periods, reducing long-term overhead costs. 🔒 Contractors bring specialised skills that may not be available in-house, allowing teams to tackle complex tasks or projects efficiently. ⚖ Teams can easily scale up or down by leveraging contractors, adapting to workload fluctuations or project demands without the need for permanent hires. 👇Reduced Training Time - contractors have industry experience, requiring minimal training and allowing teams to achieve quicker project turnaround times. 👀Fresh Perspectives: Contractors bring fresh ideas and perspectives from their varied experiences, contributing to innovative problem-solving and decision-making within the team. Stay ahead by leveraging this versatile talent pool for your short or medium-term requirements. Reach out to our recruitment experts today! enquiries@hpgconnect.com 02 8877 8777 #recruitment #medicalaffairs #regulatoryaffairs #contract #healthcare

Are there any Clinical Engineering Managers or Directors that rotate departments and/or equipment every few years among technicians? I heard that some leaders do this and was wondering how well it is working. I know this can be challenging on many fronts. Please share your thoughts and ideas on this process. This might be a good idea to discuss during a Clinical Engineering conference.

How do you safeguard your clinical trial from poor participant recruitment? In our latest blog post, we provide 4 reasons why clinical trial recruitment software can help you reach your recruitment goals faster. Our clinical trial software platform is people-centred - meaning it's easy for potential participants to see their progress, communicate with trial site members, and ultimately stay engaged throughout the recruitment process 💪 Read the full post here: https://hubs.ly/Q02d2slb0 #newblogpost #software #clinicaltrialrecruitment #clinicaltrials #Evrimatechnologies

Do you like to work as a Service Engineer in a very innovative Company with a highly innovative proprietary technology for the purpose of Drug Development and Food Research in Delft? Installing (assembly) and testing of new systems with (inter)national customers on site. Troubleshooting, maintenance and service activities of the systems at customer site and on systems in-house. 25% international travel is part of this job #serviceengineer #maintenance #installation #assembling #serviceactivities #troubleshooting #technicaljobs #mechatronics #electricalengineering #mechanicalengineering #englishspeaking

Key Components of Quality Control in Medical laboratories: Quality Control (QC) in Medical Laboratories is crucial for ensuring the accuracy and prep for test results. It involves a series of systematic procedures to maintain the reliability of labor results. This includes activities such as regular calibration of equipment, participation in proficiency testing programs, and strict adherence to standard operating procedures. Implementing Robust QC Measures is essential for identifying and correcting errors, ultimately contributing to the ove impossible and integrity of medical labor study.

Day 2/366 days 🔬⚖️ Emphasizing the Vital Role of Quality Control in Medical Laboratories 🌡️🔍 So I was reminded that this year is a leap year so basically 366 days Although I’m off duty today, I’m dedicating my time to other tasks. However, I want to underscore the critical significance of Quality Control in laboratory diagnosis. Quality Control (QC) in a medical laboratory serves as the backbone of accurate diagnostics and reliable patient care. It encompasses a series of systematic procedures and checks designed to ensure the precision and reliability of test results. The significance of QC lies in its ability to validate the accuracy and consistency of laboratory tests. Rigorous quality assurance protocols not only uphold the credibility of test outcomes but also instill confidence in healthcare professionals, ensuring they make informed decisions for patient diagnosis and treatment. By regularly monitoring and maintaining instrument calibration, verifying test performance, and validating procedures, QC mitigates errors and minimizes the risk of inaccurate results. Moreover, it complies with regulatory standards and accreditation requirements, reflecting a commitment to excellence in patient care. The continuous evolution of QC practices through advancements in technology and methodologies further enhances the reliability and efficiency of diagnostic services in medical laboratories. Let’s recognize and celebrate the indispensable role of Quality Control in ensuring precision, reliability, and utmost accuracy in healthcare diagnostics! 🌐🏥 #QualityControl #MedicalLaboratory #HealthcareDiagnostics #PrecisionMedicine #PatientCare”

LEGAL DESIGN FOR CONTRACTS Novo Nordisk, one of the leading healthcare companies in the world, approached Dot. with the task to simplify some of Novo Nordisk’s contract templates. 🗂️ THE BRIEF Novo Nordisk needed contracts that anyone could understand, without losing the legal precision they require. We gathered insights from the real users of these contracts and collaborated with their internal legal team to ensure everything was spot on. 🎯 THE GOAL We started by diving into user feedback and mapping out their needs. Then we crafted the first draft, refining it through continuous feedback until we had a streamlined, user-friendly template. 🔄 THE PROCESS The new contract templates are clear, concise, and designed with the user in mind. By cutting out the legal jargon and focusing on what truly matters, Novo Nordisk now has contracts that are not only compliant but also easy to use. --- We are back at the office and ready to help. Let’s create documents that people actually want to use. Reach out to us at hello@dot.legal or send me a DM, and let’s get started today! #legaldesign #contracts

I work very closely with a global leader in the medical device industry throughout Ireland helping them recruit for vacancies for all of their sites 🟩⬜🟧 Choosing a career in the medical device industry can be rewarding for various reasons. Here are some compelling factors to consider: ⚫Impact on Healthcare: Working in the medical device industry allows you to contribute directly to improving healthcare outcomes. Medical devices play a crucial role in diagnosis, treatment, and patient care, making a positive impact on people's lives. ⚫Innovation and Technology: The medical device industry is at the forefront of technological advancements. Professionals in this field have the opportunity to work with cutting-edge technologies, contribute to research and development, and be part of innovative solutions that can transform healthcare. ⚫Diverse Career Opportunities: The industry offers a wide range of career paths, including research and development, regulatory affairs, quality assurance, manufacturing, sales, and marketing. ⚫Global Collaboration: Many medical device companies operate on a global scale, fostering collaboration with professionals from different countries and cultures. This provides an enriching and diverse work environment, allowing for exposure to various perspectives and approaches. ⚫Regulatory Challenges: The medical device industry is subject to strict regulatory standards to ensure safety and efficacy. Professionals in regulatory affairs play a vital role in navigating these challenges, making the field intellectually stimulating and rewarding for those interested in compliance and quality. ⚫Job Stability: The demand for medical devices continues to grow as the global population ages and healthcare needs increase. This can provide a sense of job stability for individuals pursuing a career in this industry. ⚫Cross-disciplinary Collaboration: Professionals in the medical device industry often collaborate with experts from different fields, such as engineering, biology, chemistry, and medicine. This interdisciplinary approach fosters a dynamic and collaborative work environment. ⚫Continuous Learning Opportunities: The field is ever-evolving, with new technologies and research emerging regularly. This offers professionals the chance for continuous learning and skill development, keeping them engaged and up-to-date with the latest advancements in their respective areas. ⚫Competitive Compensation: Jobs in the medical device industry often come with competitive salaries and benefits, reflecting the high level of expertise and specialization required. If you are looking to make a move to the medical device industry or are already operating in it looking for your next career move, feel free to reach out to me for a confidential chat. You can contact me on 01-6933477 or at david.smith@parkerstewart.ie to arrange a call 📞

FDA Guidelines for Calibration Knowledge Share - Calibration must be performed routinely, as per written directions - Document the calibration of every device that needs calibration - Specify the acceptable limits for accuracy and precision - Train calibration personnel - Use calibration standards that are traceable to the National Institute of Standards and Technology (NIST), other acceptable standards, or in-house standards if necessary - Make provisions for evaluating adverse effects caused by malfunctioning equipment and procedures for remedial action Here at Avantor Services, Clinical Trial Equipment & Ancillary Solutions - our In-House Engineering team adopt these guidelines to ensure our inspection, measuring and test equipment is suitable for the intended purposes and capable of producing results that are valid. We take these important steps in support of our valued clinical trial customers & their global clinical studies. Note: Calibration requirements for equipment are defined by Title 21 of the FDA’s Code of Federal Regulations. According to section 820.72: #avantorsetsscienceinmotion