Cambrex: Production Supervisor https://bit.ly/45QFFDL 🌟 Exciting Opportunity Alert! 🌟 Are you a natural leader with a passion for pharmaceutical manufacturing? We are looking for a dynamic and detail-oriented Production Supervisor to join our team. In this role, you'll oversee day-to-day production activities, ensure compliance with GMP standards, and drive performance improvements. If you have a proven track record in supervising production teams and are ready to make a significant impact in a fast-paced environment, we want to hear from you! #PharmaceuticalJobs #ProductionSupervisor #CareerOpportunity #ManufacturingExcellence #JoinOurTeam #pharmiweb
Manufacturing Jobs in Life Sciences’ Post
More Relevant Posts
-
Project Manager, External Contract Research & manufacturing (Indian & Overseas). Drug products Lifecycle management for Peptides, Injectables & Orals.
Hello network, I need to connect for few roles for a initial stage pharmaceutical company with 5-10 years of experience 1. Regulatory affairs, who is having strong exposure in ROW markets in and out 2. Business development and marketing, who can able to handle all the ROW markets. please DM me to discuss further. #pharmaceuticalindustry #manufacturing #rowmarket #emergingmarkets #regulatoryaffairs #businessdevelopment #marketing #soliddosage #tablets
To view or add a comment, sign in
-
Corporate Director | Quality Management System | Pharmaceutical QP (Eligible)| Biologist | Empathetic leadership style | Big-picture thinker and forward thinker
DESIGNING A QC LAB FOR COMPLIANCE: REVIEWING INSPECTION FINDINGS- part II #FDA inspection and oversight of quality control (#QC) laboratories are essential elements of the agency’s evaluation of the #compliance status of regulated companies representing multiple industries - pharmaceuticals, biologics, medical devices, as well as foods and cosmetics - as well as the contract QC laboratories which service these industries. Lack of compliance can result in severe regulatory actions, criminal liability, fines, and the inability to obtain product approvals. What the Inspectors will check during pharmaceutical quality control laboratory Inspections #Generalinformation - The contact person (name, phone No, email) #Testactivities #Contracttesting #Ensuringsuppliersquality #Selfinspection #Trending #Changecontrol #Riskmanagement #Laboratorydocumentation #Personnel #Training #Facility #equipmentvalidation #Cleaning #Materials #Sampling #Starting/#packagingmaterials #Testing #Stabilitytesting #Validationoftestmethods #Handlingoftestresults #OutofSpecification (#OOS) #Failures #Retesting and #Resampling #Processrelease of test results #batchrelease If you like this post follow me on LinkedIn for Part III: GMP vs GLP
To view or add a comment, sign in
-
-
🔬🧪📊 #QualityControl vs. #QualityAssurance in the #PharmaceuticalIndustry: Understanding the Similarities and Differences 📝🔍🔬 #pharmaceuticalsafety #qualitymanagement #continuousimprovement
🔬🧪📊 #QualityControl vs. #QualityAssurance in the #PharmaceuticalIndustry: Understanding the Similarities and Differences 📝🔍🔬 Similarities: 1️⃣ Both #qualitycontrol and #qualityassurance are essential components of the #pharmaceutical industry. 2️⃣ Both aim to ensure that pharmaceutical products meet the required standards and regulations. 3️⃣ Both involve monitoring and evaluating processes to identify any deviations or non-conformities. 4️⃣ Both require documentation and record-keeping to maintain traceability and accountability. 5️⃣ Both involve the use of various testing methods and techniques to assess product quality. 6️⃣ Both require trained personnel with expertise in quality management systems. 7️⃣ Both focus on continuous improvement and strive for excellence in product quality. 8️⃣ Both play a crucial role in maintaining patient safety and public health. 9️⃣ Both involve adherence to regulatory guidelines, such as #GoodManufacturingPractices (GMP). 🔟 Both require effective communication and collaboration between different departments within a pharmaceutical company. Differences: 1️⃣ Quality control primarily focuses on inspecting, testing, and analyzing finished products, while quality assurance focuses on establishing systems and processes to prevent defects or errors from occurring in the first place. 2️⃣ Quality control is reactive, identifying defects after they occur, whereas quality assurance is proactive, preventing defects from happening through preventive measures. 3️⃣ Quality control involves physical testing of samples for attributes such as potency, purity, dissolution rate, etc., whereas quality assurance involves auditing processes, reviewing documentation, and implementing corrective actions based on data analysis. 4️⃣ Quality control is typically performed by laboratory technicians or analysts, whereas quality assurance is overseen by quality managers or specialists who develop policies and procedures. 5️⃣ Quality control activities are more focused on product-specific parameters, while quality assurance activities encompass broader aspects of the entire manufacturing process. 6️⃣ Quality control involves batch release testing before products can be distributed or sold, whereas quality assurance ensures that all necessary controls are in place throughout the manufacturing process. 7️⃣ Quality control deals with immediate issues related to product conformance or non-conformance, while quality assurance looks at long-term trends and systemic improvements. 8️⃣ Quality control is concerned with meeting specific product specifications, whereas quality assurance focuses on overall compliance with regulatory requirements. 9️⃣ Quality control is more concerned with the detection and rejection of defective products, while quality assurance aims to prevent defects from occurring in the first place. #pharmaceutical #safety #qualitymanagement #continuousimprovement
To view or add a comment, sign in
-
-
Three weeks into my new role and I can already tell how challenging yet rewarding this role is! While still in training and not handling projects, it's fascinating to observe my teammates' dedication in managing the high workload of GMP compliance-related investigation projects. To briefly elaborate on the importance of the role, in the unique world of GMP production, ensuring regulatory, quality, and productivity compliance is a constant focus. It's a shared responsibility within the facility to guarantee the safety, purity, and quality of pharmaceutical products reaching consumers. Therefore, even the smallest deviations from approved protocols must be diligently captured, investigated, and addressed. For those unfamiliar with the workload, while the goal is to always minimize them, deviations are more common than one might expect (which means constant monitoring, investigations, etc.). I want to say a big kudos to the incredible individuals in this chain of responsibilities. It's a pleasure to be part of this rewarding job! #gmpcompliance #pharmaceuticalmanufacturing #regulatorycompliance #newbeginnings
To view or add a comment, sign in
-
🔬🧪📊 #QualityControl vs. #QualityAssurance in the #PharmaceuticalIndustry: Understanding the Similarities and Differences 📝🔍🔬 #pharmaceuticalsafety #qualitymanagement #continuousimprovement
🔬🧪📊 #QualityControl vs. #QualityAssurance in the #PharmaceuticalIndustry: Understanding the Similarities and Differences 📝🔍🔬 Similarities: 1️⃣ Both #qualitycontrol and #qualityassurance are essential components of the #pharmaceutical industry. 2️⃣ Both aim to ensure that pharmaceutical products meet the required standards and regulations. 3️⃣ Both involve monitoring and evaluating processes to identify any deviations or non-conformities. 4️⃣ Both require documentation and record-keeping to maintain traceability and accountability. 5️⃣ Both involve the use of various testing methods and techniques to assess product quality. 6️⃣ Both require trained personnel with expertise in quality management systems. 7️⃣ Both focus on continuous improvement and strive for excellence in product quality. 8️⃣ Both play a crucial role in maintaining patient safety and public health. 9️⃣ Both involve adherence to regulatory guidelines, such as #GoodManufacturingPractices (GMP). 🔟 Both require effective communication and collaboration between different departments within a pharmaceutical company. Differences: 1️⃣ Quality control primarily focuses on inspecting, testing, and analyzing finished products, while quality assurance focuses on establishing systems and processes to prevent defects or errors from occurring in the first place. 2️⃣ Quality control is reactive, identifying defects after they occur, whereas quality assurance is proactive, preventing defects from happening through preventive measures. 3️⃣ Quality control involves physical testing of samples for attributes such as potency, purity, dissolution rate, etc., whereas quality assurance involves auditing processes, reviewing documentation, and implementing corrective actions based on data analysis. 4️⃣ Quality control is typically performed by laboratory technicians or analysts, whereas quality assurance is overseen by quality managers or specialists who develop policies and procedures. 5️⃣ Quality control activities are more focused on product-specific parameters, while quality assurance activities encompass broader aspects of the entire manufacturing process. 6️⃣ Quality control involves batch release testing before products can be distributed or sold, whereas quality assurance ensures that all necessary controls are in place throughout the manufacturing process. 7️⃣ Quality control deals with immediate issues related to product conformance or non-conformance, while quality assurance looks at long-term trends and systemic improvements. 8️⃣ Quality control is concerned with meeting specific product specifications, whereas quality assurance focuses on overall compliance with regulatory requirements. 9️⃣ Quality control is more concerned with the detection and rejection of defective products, while quality assurance aims to prevent defects from occurring in the first place. #pharmaceutical #safety #qualitymanagement #continuousimprovement
To view or add a comment, sign in
-
-
I'm Glad to Share my Certificate of Course Program on Drug Regulatory Affairs with PharmaState.Academy It was a comprehensive, informative, and beneficial course I'd like to thank the team of Pharma State Academy. Regulatory affairs is a profession within regulated industries, such as pharmaceuticals and medical devices, ensuring that their companies comply with all the regulations and laws pertaining to their business. #regulatoryaffairs #freshershiring #pharma #regulatory
To view or add a comment, sign in
-
-
Biopharmaceutical II Biotechnology II CQV Professional II Sterile Manufacturing (Drug Product) II Top Quality Assurance Voice
☝️4️⃣🅰️ Document control in the pharmaceutical industry is crucial for ensuring compliance with regulatory requirements, maintaining quality standards, and managing the vast amount of documentation generated throughout the product lifecycle. 📋✅Regulatory Compliance: Pharma companies must adhere to strict regulations set by authorities such as the USFDA, EMA and similar agencies worldwide. 📚✅Document Types: Various types of documents are generated in the pharmaceutical industry, including standard operating procedures (SOPs), protocols, batch records, validation reports, regulatory submissions, documentation, manufacturing instructions, and quality control records. 📒✅Document Lifecycle: Documents in the pharma industry typically go through a lifecycle that includes creation, review, approval, distribution, use, periodic review, and obsolescence. 📝✅Document Control Systems: Pharma companies employ document management systems (DMS) or electronic document management systems (EDMS) to facilitate document control. 🛂✅Version Control: Maintaining control over document versions is critical to ensure that users are accessing the most up-to-date information. 👉✅Access Control: Access to documents is usually restricted based on roles and permissions. Only authorized personnel should have access to certain types of documents, and access levels may vary depending on job responsibilities and the stage of the document lifecycle. 🔍✅Audit Trails: Document management systems maintain detailed audit trails that track all actions taken on documents, including creation, modification, review, approval, and distribution. 📓✅Training and Awareness: Pharma companies provide training to employees on document control procedures and the proper use of document management systems. Employees must understand their roles and responsibilities regarding document creation, review, approval, and storage. 🔄✅Change Control: Changes to controlled documents must be managed through a formal change control process to ensure that changes are properly evaluated, approved, implemented, and documented. 🔍✅Periodic Review and Retention: Documents must be periodically reviewed to ensure that they remain accurate, up-to-date, and relevant. Connect IncepBio or visit www.incepbio.com for ensuring compliance with regulatory requirements and maintain the quality standards. #pharmaceutical #biopharmaceuticals #biotechnology #medicaldevices #documentcontrol #regulatoryrequirements #maintaining #quality #standards #compliance #documents #types #sops #protocols #batch #records #reports #policy #manual #instruction #manufacturing #qc #lifecycle #controlsystems #edms #dms #review #approvals #versioncontrol #accesscontrol #audi #trail #traning #changecontrol #periodic #review #implementation Ajith K Jose Prashanth Hugar Ambarish Ghali Asish Kumar ANAND R PILLAI
To view or add a comment, sign in
-