We're hiring a Study Director and Manufacturing Associate, GMP. Visit our Careers page for more information, view all open positions, and to apply! https://bit.ly/3W8PI2T
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We're hiring a Study Director and Manufacturing Associate, GMP. Visit our Careers page for more information, view all open positions, and to apply! https://bit.ly/3W8PI2T
An excellent opportunity to work with a great team!
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Empowering Life Sciences Companies (MedTech, Pharma, Biotech) to Achieve Excellence | Solving Regulatory, Quality, and Operational Challenges | Speaker | Co-Founder of Excellence Talks & Excellence Squad
Do you need support of Excellence Squad during the holiday period? ✈️ Summer is fast approaching, and with it the holiday period for many of your employees. While your team is enjoying a well-deserved rest, we understand that your tasks can't stand still. We offer temporary support in various areas: 👉 Interim Management: Ensure your projects and operations continue smoothly with our experienced interim managers. 👉 Consultancy Services: Get expert advice and solutions tailored to your needs. 👉 Quality Assurance/Quality Management: We help you develop, implement, and audit robust quality management systems compliant with ISO standards for life sciences organizations. Our services include CAPA support, internal audits, supplier management, validation (CSV and Data Integrity), and quality strategy development. 👉 Regulatory Affairs: Customized regulatory strategies for pharmaceutical, biotech, and medical device companies. We handle global regulatory submissions, gap assessments, regulatory training, and ongoing compliance support. 👉 Product Lifecycle Project Management Support: End-to-end support from concept development to commercialization. Services include regulatory pathway assessments, product registration assistance, and compliance monitoring. 👉 Operational Excellence: Customized strategies to optimize processes, increase efficiency, and reduce costs using methodologies like Kaizen, Lean, and Six Sigma. Contact us today for an introduction. ✉️ info@xsqgroup.com #InterimManagement #Consultancy #HR #healthcare #lifescience #medtech #medicaldevices #pharma #biotechnology #quality #regulatory #excellence #ExcellenceSquad
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Empowering Life Sciences Companies (MedTech, Pharma, Biotech) to Achieve Excellence | Solving Regulatory, Quality, and Operational Challenges | Speaker | Co-Founder of Excellence Talks & Excellence Squad
Do you need support during the holiday period? ✈️ Summer is fast approaching, and with it the holiday period for many of your employees. While your team is enjoying a well-deserved rest, we understand that your tasks can't stand still. We offer temporary support in various areas: 👉 Interim Management: Ensure your projects and operations continue smoothly with our experienced interim managers. 👉 Consultancy Services: Get expert advice and solutions tailored to your needs. 👉 Quality Assurance/Quality Management: We help you develop, implement, and audit robust quality management systems compliant with ISO standards for life sciences organizations. Our services include CAPA support, internal audits, supplier management, validation (CSV and Data Integrity), and quality strategy development. 👉 Regulatory Affairs: Customized regulatory strategies for pharmaceutical, biotech, and medical device companies. We handle global regulatory submissions, gap assessments, regulatory training, and ongoing compliance support. 👉 Product Lifecycle Project Management Support: End-to-end support from concept development to commercialization. Services include regulatory pathway assessments, product registration assistance, and compliance monitoring. 👉 Operational Excellence: Customized strategies to optimize processes, increase efficiency, and reduce costs using methodologies like Kaizen, Lean, and Six Sigma. Contact us today for an introduction. ✉️ info@xsqgroup.com #InterimManagement #Consultancy #HR #healthcare #lifescience #medtech #medicaldevices #pharma #biotechnology #quality #regulatory #excellence #ExcellenceSquad
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Do you need support during the holiday period? ✈️ Summer is fast approaching, and with it the holiday period for many of your employees. While your team is enjoying a well-deserved rest, we understand that your tasks can't stand still. We offer temporary support in various areas: 👉 Interim Management: Ensure your projects and operations continue smoothly with our experienced interim managers. 👉 Consultancy Services: Get expert advice and solutions tailored to your needs. 👉 Quality Assurance/Quality Management: We help you develop, implement, and audit robust quality management systems compliant with ISO standards for life sciences organizations. Our services include CAPA support, internal audits, supplier management, validation (CSV and Data Integrity), and quality strategy development. 👉 Regulatory Affairs: Customized regulatory strategies for pharmaceutical, biotech, and medical device companies. We handle global regulatory submissions, gap assessments, regulatory training, and ongoing compliance support. 👉 Product Lifecycle Project Management Support: End-to-end support from concept development to commercialization. Services include regulatory pathway assessments, product registration assistance, and compliance monitoring. 👉 Operational Excellence: Customized strategies to optimize processes, increase efficiency, and reduce costs using methodologies like Kaizen, Lean, and Six Sigma. Contact us today for an introduction. ✉️ info@xsqgroup.com #InterimManagement #Consultancy #HR #healthcare #lifescience #medtech #medicaldevices #pharma #biotechnology #quality #regulatory #excellence #ExcellenceSquad
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Do you need support during the holiday period? ✈️ Summer is fast approaching, and with it the holiday period for many of your employees. While your team is enjoying a well-deserved rest, we understand that your tasks can't stand still. We offer temporary support in various areas: 👉 Interim Management: Ensure your projects and operations continue smoothly with our experienced interim managers. 👉 Consultancy Services: Get expert advice and solutions tailored to your needs. 👉 Quality Assurance/Quality Management: We help you develop, implement, and audit robust quality management systems compliant with ISO standards for life sciences organizations. Our services include CAPA support, internal audits, supplier management, validation (CSV and Data Integrity), and quality strategy development. 👉 Regulatory Affairs: Customized regulatory strategies for pharmaceutical, biotech, and medical device companies. We handle global regulatory submissions, gap assessments, regulatory training, and ongoing compliance support. 👉 Product Lifecycle Project Management Support: End-to-end support from concept development to commercialization. Services include regulatory pathway assessments, product registration assistance, and compliance monitoring. 👉 Operational Excellence: Customized strategies to optimize processes, increase efficiency, and reduce costs using methodologies like Kaizen, Lean, and Six Sigma. Contact us today for an introduction. ✉️ info@xsqgroup.com #InterimManagement #Consultancy #HR #healthcare #lifescience #medtech #medicaldevices #pharma #biotechnology #quality #regulatory #excellence #ExcellenceSquad
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Mitra S K's Laboratory Consultancy Services provide expert guidance to optimize lab operations. Our team specializes in Laboratory Management, Regulatory Affairs, Quality Control, and Assurance. We ensure compliance and efficiency tailored to your organization's needs. #labconsultancy #optimizeoperations #expertguidance #regulatorycompliance #qualitycontrol #qualityassurance #efficiency #tailoredsolutions
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🔍 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
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Life Science Global Stream Leader - Process Equipment & Technology Providers (CQV Automation & Engineering) | AI/IA/Machine Learning Passionated | 𝟙4 Years ꮖ🇳 𝓢𝓘𝓝𝓖𝓐𝓟𝓞𝓡𝓔 | Ꮇ𝒶𝓃𝒶𝑔𝑒𝓂𝑒𝓃𝓉 ℰ𝓃𝑔.
🌟 Why you Should Choose PQE Group as your Partner 🌟 Are you in the Life Sciences industry? Partnering with PQE Group can give you the competitive edge you need. Here’s why: Comprehensive Technical Expertise: - GMP Compliance: We ensure your manufacturing processes meet the highest standards of Good Manufacturing Practice. - Process Engineering: Our team excels in designing and optimizing efficient, scalable processes tailored to your needs. - CQV Services: Commissioning, Qualification, and Validation services to ensure your facilities and equipment are up to regulatory standards. - Regulatory Affairs: Expertise in navigating complex regulatory landscapes, ensuring your products meet all necessary requirements. - Quality Assurance: Robust QA services to maintain the highest quality standards across all operations. - Data Integrity: Ensuring the accuracy, completeness, and reliability of your data for compliance and operational efficiency. - Risk Management: Identifying, assessing, and mitigating risks to safeguard your operations and products. - Training Programs: Customized training solutions to empower your team with the latest industry knowledge and best practices. Global Reach, Local Presence: With a global network and local expertise, we can support your operations no matter where you are in the world. 🌍 Innovation-Driven Approach: Our forward-thinking solutions and cutting-edge technology ensure your startup remains ahead of the curve. Dedicated Support: From initial setup to full-scale operations, we provide continuous support to help you achieve your goals. Ready to elevate your startup in the Life Sciences industry? Let’s connect and explore how PQE Group can be your trusted partner on this exciting journey. #LifeSciences #Startup #Pharmaceutical #ProcessEngineering #Compliance #GMP #CQV #RegulatoryAffairs #QualityAssurance #DataIntegrity #RiskManagement #Training #Innovation
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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
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Helping Head of Quality / Quality Directors Transition from Crisis Managers to Strategic Leaders with the Core Competence System | LMS | PQS | GxP
🌟 Transforming Quality Management at GeneriPharm Ltd. 🌟 (note all names changed for privacy) 🔍 Stage 1: Initiation Kicked off with a strategic meeting where our expert auditor, Alex Reed, outlined the audit's scope with GeneriPharm’s management team. Aiming high from day one! 🚀 🔧 Stage 2: Inspection Alex took a deep dive into the manufacturing processes, identifying key areas for improvement. His thorough inspection on the factory floor identified critical deficiencies in documentation, training, and equipment maintenance. 🏭 📚 Stage 3: Training We rolled out an engaging training program, empowering the with new working practices and tools to enhance documentation accuracy and compliance. The standard operating procedures were updated appropriately with a focus on knowledge management. Knowledge is power! 🧠 💬 Stage 4: Culture Shift We introduced "huddles" encouraging all them members to speak-up, cultivating an open and proactive culture where everyone feels safe to voice concerns and suggestions. A real game-changer in nurturing a positive workplace! 🌱 📈 Stage 5: Results & Celebration The follow-up audit was a resounding success, showcasing significant improvements in compliance and operational efficiency. Ending on a high note with a celebration that marked a new chapter of quality and excellence at GeneriPharm Ltd.! 🎉 (in case you missed it all names have been changed for privacy) --- 🔗 I obsess over delivering best in class performance, follow me @paulrpalmer for more insights into the pharmaceutical industry. #QualityAssurance #Pharmaceuticals #Leadership #Innovation #ContinuousImprovement
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Brand partnership • || US Technical Recruiter ( Non IT & IT ) || Pharma || Medical Device || Life Science Staffing Specialist || helps for job seeker's
🌟 Top Talent Available for New Opportunities! 🌍 Open to Relocation! 🔍 Presenting skilled professionals adept in: Quality Management, GMP, CAPA, and ISO Standards Lean Manufacturing, Six Sigma, and Continuous Improvement Equipment and Process Validation, Cleaning Validation, and CSV Process Optimization, Engineering, and Control R&D, Product Development, and innovation Regulatory Affairs, FDA Compliance, and Submissions NPI Planning, Design Transfer, and Collaboration Supplier Quality, Audits, and Risk Management CQV: Commissioning, Qualification, and Validation 🚀 Ready to drive your team's success! Connect with me at Venkatateja@novozen.com or DM for more details. Venkata Teja | Life science Recruiter Novozen Healthcaren LLC Ph: +1 732-746-0641 Email: vekatateja@novozen.com #TopTalent #JobSeeker #RelocationOpportunity #QualityManagement #GMP #CAPA #ISOStandards #LeanManufacturing #SixSigma #ContinuousImprovement #ValidationExperts #ProcessOptimization #EngineeringSkills #RnD #ProductDevelopment #Innovation #RegulatoryAffairs #FDACompliance #NPIPlanning #DesignTransfer #Collaboration #SupplierQuality #Audits #RiskManagement #CQV #Commissioning #Qualification #Validation #CareerMove #OpportunityKnocks #NewBeginnings #CareerGrowth #ProfessionalDevelopment #TeamPlayer #LeadershipSkills #SuccessDriven #ConnectWithMe #OpenToRelocation #CareerAdvancement #StrategicThinking #IndustryExperts #GlobalTalent #Networking #TechSkills #LinkedInConnection #ProfessionalNetwork #NewChallenges #DreamJob #AchievementUnlocked #JoinMyTeam #InDemandSkills #CareerBoost #FutureLeadership #JobOpportunities #LetsConnect #CareerLeap #ExploreOpportunities #ProfessionalJourney #SkillsShowcase #IndustryInsiders #YourNextHire #JobSearchJourney #CareerAdvise
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Strategic Sales | Account Management | Customer Success | Consulting | Business Development | Relationship Building | CliftonStrengths: Connectedness, Activator, Strategic, Learner, Woo
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