Regulatory Affairs Jobs in Life Sciences’ Post

Do you want to start a career as a Quality Assurance Specialist in Pharma? Well, in the world of Pharma, Quality Assurance (QA) is not just a role, but a mission. It's the silent guardian of health and safety, ensuring every medication we trust is up to the mark. 🛡️💊 QA in Pharma is where precision meets care. It's about maintaining the highest standards in every pill and potion. From rigorous processes to meticulous documentation, QA professionals are the unsung heroes behind every successful product. 🌟🔬 Discover the significance of QA in Pharma 📚 🔗www.pharmuni.com #QualityAssurance #PharmaHeroes #HealthcareSafety #PharmaceuticalQuality

We know very well, the critical role that a Quality Assurance Specialist plays in the world of #pharma. I have seen first hand the difference a good QA specialist can make and I have also seen some not so great examples. That is why all of our QA team go through a rigorous onboarding, complete the Pharmuni #qualifications for the QA specialist and receive regular upskilling. Just as we believe in the power of knowledge as a key driver to success, the QA leadership and Management team at Zamann Pharma Support also believe education and support to be foundations for growing your teams and developing them into experts. #educate #developers #nurture #qualityassurance #pharma

Quality assurance in the pharmaceutical industry is more than just a job - it is a 100% commitment to quality.

MEDICAL DEVICE CONTRACTORS AVAILABLE! - Quality Assurance - Regulatory Affairs - Validation The majority of these contractors have successfully completed projects for Real Staffing's clients, and are extremely well referenced. If you are interested to see any of these profiles or discuss your requirements - please reach out for a chat! #staffing #hiring #medicaldevices #quality #regulatory #validation

Hi, Hope you are doing great! This is Ram working as a Pharma and Medical Device Recruiter for Sahasa IT, From Sahasa IT we provide top-notch talent in the following areas: 1. Validation Engineer - Equipment, Cleaning, and Process 2. Engineers - Quality, Manufacturing, Process 3. Regulatory Affairs - Medical Devices and Drugs 4. Computer System Validation 5. Drug Safety Associates 6. Clinical SAS 7. Clinical Research Associates 8. Clinical Data Management If you have any Contract roles on the above-mentioned skills, feel free to reach out to me at [email protected] or Call 1 (720-915-0784). #Pharmaceutical #Healthcare #CAPA #Iso13485 #Iso14971 #FMEA #PFMEA #DFMEA #EUMDR #FDA #QSR #Part820 #21CFR #DHF #IQ #OQ #PQ #GxP #GAP #GAMP #GMP #CGMP #GPvP #TMV #RCA #NCR #NCMR #NPD #SPC #GDP #EUMDR #MDD #STED #GCP #CSV #SQE #Regulatory #DMF #MHRA #RA #GCDMP #CQV #CSV #Commissioning #Qualification #Equipment #Clinical #Research #Associates #Computersystemvalidation #Clinical #Data #Management #Regulatory #Affairs #Drug #Safety #Associates #USA #USAjobs #Contract #c2cjobs #c2copportunities #c2c #medical #Pharma_Recruiter #recruitment #jobs #marketing #socialnetworking #jobinterviews #business #hiring#QualityManagement #RnD #ProductDevelopment #FDACompliance #SupplierQuality #RiskManagement #CQV #Validation #TechSkills #LetsConnect #ExploreOpportunities #JobSearchJourney #MedicalDevice

This week we are tackling Regulatory Affairs!! Reach out for more information or if you enjoyed reading this, jump in and contribute to the conversation!!! #qualityassurance #qa #compliance #regulatorycompliance #regulatoryaffairs #lifesciences #pharma #recruitment #qc #qualitycontrol

As a #Quality_Assurance (#QA) #biomedicalengineer, #المهندس_عبدالله_عبدالرحمن your primary role is to ensure that medical devices, equipment, and processes meet regulatory standards and perform safely and effectively. Testing and Validation: Conducting tests to verify that biomedical equipment and devices meet specifications and standards. This includes functional testing, performance testing, and reliability testing. Regulatory Compliance: Ensuring that all products adhere to relevant regulations and standards set by organizations like the #FDA (Food and Drug Administration) or international standards such as #ISO (International Organization for Standardization). Documentation: Maintaining detailed records of testing procedures, results, and compliance documentation. This documentation is crucial for regulatory submissions and audits. Risk Management: Identifying and assessing potential risks associated with biomedical products or processes and implementing measures to mitigate these risks. Process Improvement: Continuously evaluating and improving quality control processes to enhance efficiency and ensure the highest level of product quality. Collaboration: Working closely with cross-functional teams including R&D, manufacturing, and regulatory affairs to address quality issues and ensure compliance throughout the product lifecycle. #biomedicalengineering #biomedicalengineer #medicalEquipment #medicaldevices #abdallahabdelrahman #medicalimaging #laboratories #clinicalengineer #fieldserviceengineer #HealthCare #Healthcaretechnology #hospital #bme

Hello Everyone, There are numerous kinds of definitions of regulatory affairs. One concept I'd like to draw attention to is that Regulatory Affairs is a career in which an individual must interact with both internal and external departments to ensure that all requirements are in compliance with certain regulations and standards. The following images detail the individuals with whom the RA professionals communicate, including both internal and external departments.  The comment box is open to add other stakeholders or departments that RA personnel are involved with. "Follow for more information on regulatory affairs articles" #regulatoryaffairs #usfda #fda #clinical #research #development #engineering #medical #medtech #biomedical #regulatory #regulations #quality #qa #management #healthcare #communication