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Inviting candidates for the post of Executive / Sr. Executive for #TechnologyTransfer Quality Assurance Department, Ciron Drugs & Pharmaceuticals Pvt. Ltd. Manufacturing plant at Boisar. #Role: Technology Transfer Executive / Sr. Executive #Qualification: B. Pharm / M. Pharm #Experience: 2-8 years of experience. #Salary: Depends on Interview. Candidates should experience in handling and implementing cGMP (current Good Manufacturing Practice) practices and Good Documentation Practices. #JobResponsibility:  • Scaling up technology Transfer and exhibiting batches for commercial products.  • Site transfer of approved products from one facility to another facility.  • Evaluating and selecting optimal batch sizes for scaling up using scientific scale up techniques as guidance based on manufacturing process and equipment capacities for registration batches and launch commercial production. • Preparing and reviewing Master batch documents, validation protocols and reports related to submission batches and process validation.  • Coordinating with regulatory, production, PPIC, QC, QA and other functions for Technology Transfer activities. • Revalidating, technical trouble shooting, batch size changes and alternate vendor development. #techtransfer #QA #QC #regulatory #validation #processvalidation #qualityassurance #cirondrugs #ciron #injectable #eyedrops #vail #amplouses #production #GMP #cGMP #revalidating #technical #batches

Please join hands together to welcome our special Guest Speaker, Mr. Vikrant Singh Parmar for our "Pharma Talk" Series. Mr. Vikrant is contributing to industry as a Deputy General Manager specializing in Global Quality Investigations, possessing the capability to propel and attain the highest standards through efficient management. With nearly 18 years of hands-on experience in the Quality domain, specifically in Parenteral and Oral dosage forms, he has honed a profound understanding of critical quality investigations. This encompasses expertise in #Lab and #Manufacturing #investigations, #Data #Integrity #Assurance, Quality Management Systems #qms, Quality System Remediation, #Document Management, #Quality Operations, #Validation/Qualification, #Audit and #Compliance, Quality Lab Assurance, #IT Compliance, The topic is "Data Integrity Issues" Stay tune with us. #cpf #speaker #centerofpharmaforce #knowledge #learning #growtogether #pharma #pharmaceuticals #pharmajobs #pharmaceuticaljobs #pharmaindustry #pharmacist #pharmacistjobs #pharmacistlife #motivation #inspiration #Guestspeaker #dataintegrity #itqa #itcompliance #compliance #audit #lab #qms

🌟 Uncover the daily wonders of Qualification and Validation. At our workshop Seamlessly integrate the latest guidelines into your work, ensuring not only efficiency but also meeting regulatory standards. Empower your professional journey with knowledge that matters every day. 📊🔍Advance Your Career – Enroll now! 📞 For more details and to secure your spot, contact us: +201550853888 📱 +201020871520 📱 #valoregypt #QualificationAndValidation #PharmaCourses #PharmaProfessionals #ProfessionalDevelopment #PharmaceuticalIndustry #QualityManagement #QualitySystems #QualityAssurance

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

Are you ready to start 2025 ensuring that your product meets (or exceeds) industry quality assurance (QA) standards? QA in life sciences plays a crucial role in ensuring that products, services, and processes meet regulatory standards and deliver safe, effective, and reliable results. Test your organization’s QA readiness!   (Go to carousel) If you answered ‘no’ to any of these situations, it’s a good time to focus on QA. At BioBridges, we have experienced quality assurance professionals who can help ensure your clinical development is ready for 2025.  Learn more at www.biobridges.com    #QualityAssurance #RegulatoryCompliance #LifeSciences #ClinicalDevelopment #Pharma #MedTech 

A Validation Engineer ensures that systems, processes, or products meet specified requirements and standards. They typically work in industries like pharmaceuticals, biotechnology, and manufacturing, focusing on validating equipment, methods, and software. Key Responsibilities: Develop Validation Protocols: Create and execute protocols for validating systems and processes. Conduct Tests: Perform qualification and validation tests to ensure compliance with regulatory standards. Document Findings: Maintain thorough documentation of validation activities, results, and deviations. Collaborate: Work closely with cross-functional teams, including quality assurance, production, and regulatory affairs. Regulatory Compliance: Ensure compliance with industry regulations such as FDA, ISO, or GMP standards. Skills Required: Strong analytical and problem-solving abilities Attention to detail Knowledge of relevant regulations and guidelines Excellent communication skills Career Path: Validation Engineers often have backgrounds in engineering, life sciences, or a related field and may advance to roles such as Validation Manager or Quality Assurance Manager. Validation Engineering: #ValidationEngineer #QualityAssurance #GMP #Pharmaceuticals #ProcessValidation #SoftwareValidation #RegulatoryCompliance #QualityControl #Engineering #Biotechnology #Validation #IndustryStandards #RiskManagement #Cleanroom #LeanSixSigma

🔍 Opportunities in Quality Control 🔍 The demand for quality control professionals in biotech and pharmaceuticals is on the rise! As companies strive to meet rigorous regulatory standards and ensure the highest product quality, the role of QC teams is more critical than ever. At Viltis, we recognize the importance of maintaining excellence in quality, clinical, and regulatory areas. Whether you’re a seasoned QC expert or just starting your career, now is an exciting time to explore opportunities in this field. Check out this article from BioSpace highlighting 9 companies currently hiring for quality control positions: https://lnkd.in/gmJmMvpe As always, Viltis is here to support your journey in Quality, Clinical, Regulatory, Engineering, and Scientific areas. Let's work together to push the boundaries of what's possible in healthcare! #QualityControl #BiotechCareers #Viltis #HealthcareInnovation #QualityAssurance #RegulatoryAffairs

🌟 #Elevating_Quality, #Ensuring_Excellence 🌟 As a Quality Control Chemist, I’m passionate about setting high standards and ensuring every product that leaves the lab meets rigorous quality benchmarks. In my role, I've tackled diverse challenges—implementing advanced calibration techniques, conducting in-depth analytical method validation, and developing SOPs to maintain top-tier quality in all processes. 🧪 My key areas of expertise include: - Analytical Method Validation & Verification: Upholding accuracy through robust testing and validation procedures. - Comparative Dissolution Profiling: Aligning in-house product standards with industry leaders per FDA and WHO guidelines. - Technology Transfer & Stability Testing: Bridging R&D and QC for seamless quality assurance in product stability. If you’re in the pharmaceutical, manufacturing, or quality control sectors, I’d love to connect! Whether it’s for sharing best practices, exploring collaborative projects, or simply expanding our professional networks, I’m always excited to learn and contribute. Let’s connect and drive quality to new heights! 🚀💼 #QualityControl #Chemistry #Pharmaceuticals #AnalyticalChemistry #QualityAssurance #OpenToConnections #Chemist

Isn't it shocking that 46% of the employees in Pharma field haven't learnt a new skill in last one year? AptSkill is on its mission to impart quality training to the Pharma and Medical Devices professionals and improving the skill development scenario of the industry! #Pharma #MedicalDevices #SkillDevelopment