Manufacturing Jobs in Life Sciences’ Post

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

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

From Quality Assurance to Regulatory Consulting: A Journey of Precision and Compliance As someone who spent majority of experience in the Quality Assurance department of a pharmaceutical manufacturing company 🏭, I’ve come to truly appreciate the importance of compliance, precision, and attention to detail. These core values, which are the backbone of any QA role, have seamlessly translated into my current work in regulatory consulting 📑💼. In QA, I was responsible for ensuring that every product met the highest standards✅, adhering to stringent regulations and quality protocols. This experience honed my ability to: - Interpret regulatory guidelines effectively 📋 - Maintain meticulous documentation 📝 - Collaborate across teams 🤝 to ensure compliance - Problem-solve under tight deadlines ⏳ Now, in regulatory consulting, these skills are even more critical. Whether it's navigating complex regulatory landscapes 🌍 or ensuring that clients meet the necessary compliance requirements, my background in QA gives me a unique edge 🏆. The shift from QA to regulatory consulting has been both challenging and rewarding, but it has also shown me how interlinked these two fields are. Understanding the intricacies of quality processes has allowed me to offer more comprehensive, practical solutions to clients navigating global regulatory requirements 🌐. Looking forward to sharing more insights from my journey! Would love to hear your thoughts on how Quality Assurance has influenced your career path. #RegulatoryConsulting #QualityAssurance #Pharmaceuticals #Compliance #CareerJourney

General Knowledge of pharma QA

General Knowledge of pharma QA

#hiringalert Job Title - #QC Reviewer Experience - 5 to 10 Years Salary Range - up to 8 LPA Job Location - Chandigarh Industry - API Regulatory Plant #KeyResponsibilities: - Review and Approval of Analytical Data: Scrutinize analytical data generated during the testing of raw materials, intermediates, and finished API products to ensure accuracy, precision, and compliance with specifications. - #DocumentReview: Review and approve laboratory notebooks, test methods, specifications, standard operating procedures (SOPs), and other relevant documentation to ensure compliance with regulatory requirements and company standards. - #InvestigationSupport: Assist in the investigation of out-of-specification (#OOS) results, #deviations, and laboratory incidents by providing technical expertise and contributing to root cause analysis. - #QualityCompliance: Ensure that all QC activities are performed in accordance with Good Manufacturing Practices (#GMP), Good Laboratory Practices (#GLP), and other applicable regulatory guidelines. - #Method #Validation and #Verification: Participate in method validation and verification activities, reviewing protocols, reports, and data to ensure the reliability and suitability of analytical methods. - #Instrument #Calibration and #Maintenance: Oversee the calibration, qualification, and maintenance of analytical instruments to ensure accurate and reliable results. - #Training and #Development: Provide training and guidance to QC personnel on quality systems, procedures, and regulatory requirements to enhance their understanding and performance. - #Continuous #Improvement: Identify opportunities for process improvements within the QC function, proposing and implementing corrective and preventive actions to enhance efficiency, accuracy, and compliance. - #Cross-functional Collaboration: Collaborate with other departments, including Quality Assurance (QA), Regulatory Affairs, Manufacturing, and R&D, to address quality-related issues, support product development, and facilitate regulatory submissions. Audit Support: Support internal and external audits by providing documentation, data, and technical expertise, and participating in audit observations and corrective action implementation. #Qualifications and #Skills: - Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field. - Previous experience in quality control or quality assurance within the pharmaceutical industry, with specific experience in API manufacturing preferred. - Strong understanding of analytical techniques and instrumentation used in pharmaceutical analysis. - Knowledge of regulatory requirements, including FDA, EMA, and ICH guidelines. Interested candidates can share their profile at [email protected] or can WhatsApp at 8629031243 #gntpage #gntjobs #qcreviewer #pharmaceuticals #APIIndustry #Qualitycontrol

Nerhadou International, 6th of October, Giza GMP Senior Compliance Specialist Job Description Investigation the deviations received from different departments, investigation & root cause analysis & review of reports to be reviewed by compliance supervisor. Implementation of CAPA system, ensure that all approved CAPAS are tracked and communicated to all concerned parties & follow-up of CAPA plans implementation and effectiveness. Implement change control system, evaluation of changes & checking appropriate timeline implementation. Implement of product quality review plan and initiate reports annually for all products. Investigation of customer complaints. Implementation of the plan for quality risk management in production areas, warehouses & Quality control, Ensure that all potential and existing quality risks are tracked, Review quality risk management reports to be evaluated by compliance supervisor. Ensure compliance with GMP pharmaceutical guidelines and ISO Standards, Quality Management System and Data Integrity tracking of vendor management / supplier evaluation system including raw/ packaging materials suppliers, toll manufacturers, Bio-equivalence centres and other service providers. Participate in Handling external audits from different local and external regulatory bodies and licensors. tracking quality agreement with suppliers to ensure all contractual quality requirements are fulfilled. Implement the system for qualification of outsourced activities s and suppliers according to pre-set criteria and follow up annual performance to issue updated approved list. Share in Internal audit program, plan issuance and execution, follow up of CAPA implementation. Job Requirements Proven work experience as a Compliance Specialist or similar role Strong analytical and critical thinking skills Excellent verbal and written communication skills Documenting and reporting skills Computer knowledge Good English language Proficiency in MS Office (MS Excel & word) https://lnkd.in/dTU3EfMV #manufacturing #vacancy #pharmaceutical #recruiting #jobvacancy #jobalert #vacancy #qualitycontrol #qualitycontrolanalyst #qualityanalyst #Otsukapharmaceutical #Obourcity #QC #QCanalyst #regulatoryaffairs #pharmaceuticalindustry #pharmaceutical #CTD #cmc #Regulatory #Pharma #pharmacy #science #Hiring #vacancy #pharmaceuticals #pharmacist #pharmaceuticalmanufacturing #hospital_pharmacist #hospitals #qualitycontrol #quality_control #veterinarymedicine #qualitysystems #qualityassurance #quality_control_professional #egypt #sciencejobs #sciencejobs #pharmaceutical #pharmaceuticalindustry #pharmaceuticalmanufacturing #pharma #pharmacy #pharmacists #sciencejobs #biochemistry #agriculture #agriculturelife #fresherjobs #freshers2024 #freshers2023 up, mention and share please follow to see more jobs #antonious_fares

Hello "Medical Device" "Recruiters"! 👋🏻 We bring top-tier engineering talent to elevate your upcoming projects! Our elite team is primed and ready to make a significant impact. Whether you need Packaging Engineers, Validation Experts, or Manufacturing Engineer, We've got it all covered. 🔺 Validation Engineer 🔺 Cleaning Validation 🔺 Packaging Engineer 🔺 CSV Engineer 🔺 Manufacturing Engineer 🔺 Process Engineer 🔺 Product Development Engineer 🔺 Quality Engineer Show your support by "liking" this post and We'll send you the "Hotlist" of our available consultants to keep you in the loop! Let's connect these experts with your "Corp" to "Corp" ("C2C") needs. Share your requirements with us at [email protected] 📩 Connect with me, Srikar Reddy, for daily updates on consultant availability. Thanks & Regards Srikar Reddy Insight Sales Lead | WissenIt Inc Office:  1 (980) 381-4058 Ext: 662 #csv #csvengineer #validation #qualityanalyst #qa #pharma #recruiters #technicalrecruiter #21cfrpart11 #fda #medical #pharma #pharmaceutical #veevavault #hpalm #jira #gamp5 #trackwise #lims #c2c #regulatorycompliance #regulatoryaffairs #c2crequirements #corp2corp #open #regulatoryaffairs #quality #projects #packaging #medical #medical #consultants #writer #meddevice #medicaldevices #pharmaceutical #biotechnology #validation #cfr #riskanalysis #sdlc #changemanagement #urs #validationengineer #usa #uscitizens #greencard #experienced #pharmaindustry #medical #c2c #quality #qaengineer #validationengineer #validationconsultant #csv #medicaldevices #pharma #csvengineer #capa #gxp #gmp #fmea #eumdr #regulatorycompliance #iso #regulatoryaffairs #tester #EHS #Engineer #pharma #OPT #CPT #H1Bhashtag #H4hashtag #GChashtag #USChashtag #opentorelocate #hashtag #Medhashtag #pharma #hashtag #lifescience #hashtag #c2c

good opportunity