We're #hiring a new Laboratory Quality Specialist in Atlanta, Georgia. Apply today or share this post with your network.
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Great Leadership Opportunity
Leadership | Clinical Laboratory Management | Process Improvement | Quality Management | Strategy Development | Efficiency | Regulatory Compliance
Great clinical laboratory leadership opportunity as Quality Manager. Please see link below for details. https://lnkd.in/eVkUgKPD
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As challenged by Priscillar Mcmillan 📌I want to define myself and what I offer. 1. I am a Laboratory Technologist (lab analyst) 2. I am passionate about quality assurance and safety.Ensuring that highest level of quality is met!As a lab tech it is my duty that the service or product is per standard before it meets the customer/client. 3. I am driven by the love for Science,love for my family and making a positive impact in my community. 4. I am known for my analytical skills!My ability to collect,Analyze and interpret test results. 5. I help in providing guidance on laboratory procedures.Not only that,I'm also a team player and this helps in bringing everyone around and leaving no one behind while working. 6. I create an environment suitable for work.I play an important role in delivering accurate and reliable test results.
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Joulé is #hiring a Quality Control Analyst II! Responsibilities: 🔬 Analytical Testing: Conduct analytical testing and data verification for in-process, release, raw materials, and stability programs. 🧪 Advanced Techniques: Perform testing using HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, and ELISA. 🤝 Cross-Department Collaboration: Work with various teams to address project issues, lab investigations, and process improvements. 📋 Compliance & Investigations: Document and investigate Out of Specification results, deviations, and implement corrective actions. 📑 Regulatory Support: Assist in preparing for regulatory inspections and agency interactions, including dossier preparation. ⚙️ Equipment Maintenance: Ensure laboratory equipment is well-maintained and adhere to company policies and regulatory standards. #JouleAllDay #QualityControl #OpenToWork #NewJersey
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🤔Some mid week thinking....take a look at some of the opportunities that are on offer here with #Lilly Cork? 📍 Located in Little Island, Cork, the Global Business Solutions team of over 1,600 optimize and add value to key business operations across the #Lilly company. If you are a Scientist with CMC experience, I want to hear from you. 𝑪𝒍𝒊𝒄𝒌 𝒐𝒏 𝒕𝒉𝒆 𝒍𝒊𝒏𝒌𝒔 𝒃𝒆𝒍𝒐𝒘 𝒕𝒐 𝒕𝒐 𝒂𝒑𝒑𝒍𝒚 𝒕𝒐 𝒕𝒉𝒆 𝒐𝒑𝒆𝒏 𝒓𝒐𝒍𝒆𝒔: 𝐏𝐫𝐢𝐧𝐜𝐢𝐩𝐚𝐥 𝐒𝐜𝐢𝐞𝐧𝐭𝐢𝐬𝐭 - 𝐂𝐌𝐂 𝐏𝐫𝐞-𝐚𝐩𝐩𝐫𝐨𝐯𝐚𝐥 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 👉 https://e.lilly/3XFzPD4 𝐏𝐫𝐢𝐧𝐜𝐢𝐩𝐚𝐥 𝐒𝐜𝐢𝐞𝐧𝐭𝐢𝐬𝐭 - 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲, 𝐆𝐑𝐀 𝐂𝐌𝐂 👉 https://e.lilly/4cTYU1H #WeAreLilly #CMC #Scientist #preapproval #regulatory #Postapproval
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Opportunity
Happy Friday!! 🎃 Exciting job opportunities available this week in the biotech industry: 🔹 QA Associate (Overnight), GMP biologics - Novato, CA 🔹 Quality Compliance Specialist - Novato, CA 🔹 Bioinformatics Engineer - Foster City, CA 🔹 Computational Biologist - SSF, CA 🔹 Validation Engineer - Tucson, AZ 🔹 Formulations SRA - SSF, CA 🔹 QC Stability Manager - Redwood City, CA If you're interested in any of these positions, feel free to send me your resume at cgladd@r-dpartners.com, and let's schedule a time to chat! #Biotech #JobOpportunities #CareerGrowth
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A leadership turnover rate of just 9% is exceptionally low. As the market recovers, we can anticipate a notable increase in leadership transitions, particularly in the quality and regulatory sectors of medical device companies.
Interesting job market for leaders of quality and regulatory.
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🔍 Top 3 Skills Required for Quality Engineer Job in Medical Device Industry 🔍 Are you aiming for a career as a Quality Engineer in the dynamic and impactful Medical Device industry? Here are the top 3 skills you need to succeed: 1. Regulatory Knowledge 📜 Understanding FDA, ISO 13485, and other regulatory requirements is crucial. Staying updated with compliance standards ensures the safety and efficacy of medical devices. 2. Analytical Skills 🔍 Strong problem-solving abilities and proficiency in data analysis are essential. These skills help in identifying potential issues and implementing effective solutions to maintain quality. 3. Attention to Detail 🧐 Precision and thoroughness are key. A meticulous approach ensures that every aspect of the device meets high-quality standards, reducing the risk of defects and enhancing patient safety. Develop these skills to excel and make a meaningful impact in the Medical Device industry! #Hiring #Medicaldevice #QualityEngineer #GroveTechnicalResources
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What no one tells you about being a technical recruiter is that your google algorithm gets really messed up. To recruit on our positions we often have to do a lot of googling about various subjects to learn enough to have a decent conversation with candidates. After a while you start getting ads for laboratory instrumentation, HPLC columns, various pharmaceuticals, and a litany of other random things. When Thermofisher is advertising between Ms Rachel videos (if you know you know #toddler) you might have a problem. On another note there are multiple heat advisories across NorCal this week. Its super hot... You know what else is hot? Our jobs! Scientist I - Yeast Display - Bay Area SRA/RA - Phage & Yeast Display - Bay Area 2 X Analytical Chemist (contract to hire) - Sacramento Formulations Chemist - Columbus, Ohio Hit up my Calendly in my profile or comments, DM, or email me at Jeff@cofactorrecruitment.com Lets Connect!
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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
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The Vital Role of a Technical Supervisor in a High-Complexity Clinical Laboratory Through our visits to numerous clinical labs, we've observed the challenges many face in addressing deficiencies identified during CLIA, CAP, or COLA inspections, alongside the daily demands of reporting clinical test results. A key issue we've identified is that many labs opt for free or low-cost validation services offered by reagent companies when purchasing their products. However, these companies typically perform only analytical validation, often cutting corners by not using control samples that accurately represent clinical specimens. As a result, crucial aspects such as clinical validation, accuracy, stability, interference, and cut-off evaluations are frequently missing from validation reports. Labs may only become aware of these shortcomings after an inspection or, worse, after processing numerous patient samples without fully understanding the accuracy of their tests. While a Lab Director can serve as a Technical Supervisor, many fulfill this role remotely and only visit the lab a few times a year. This absence becomes problematic when technical issues arise, as they are not physically present to evaluate and implement corrective actions. This is where the role of an on-site Technical Supervisor becomes indispensable. They ensure the lab's quality by maintaining rigorous quality assurance and control standards. Contact us for Technical Supervisor services. With years of experience in clinical settings, we will support you in selecting an appropriate test menu, and implementing cost-effective yet highly accurate testing processes, ensuring you are well-prepared for any inspection. info@avicennalabconsulting.com #CLIA #CAP #COLA #clinicallaboratory #validation #infectiousdisease #genetictesting #QPCR #NGS #labdirector #technicalsupervisor
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