Quality (QA/QC) Jobs in Life Sciences’ Post

Is 2024 the year with a huge hiring budget? If not, we have brilliant experts to support you! 🔹 Regulatory Project Manager 🔹 Global Regulatory Lead 🔹 Clinical Regulatory Expert 🔹 Regulatory CMC Expert 🔹 Labelling Specialist We offer flexible service models based on your needs: ✔ FTE/partial FTE insourcing ✔ Project support ✔ Specialist consulting Does your regulatory team need support? Let's connect! [email protected] #regulatoryaffairs #drugdevelopment #qualityassurance  #pharmacovigilance #pharma #pharmaceuticals #biotech #marketaccess #pharmabusiness

Is 2024 the year with a huge hiring budget? If not, we have brilliant experts to support you! 🔹 Regulatory Project Manager 🔹 Global Regulatory Lead 🔹 Clinical Regulatory Expert 🔹 Regulatory CMC Expert 🔹 Labelling Specialist We offer flexible service models based on your needs: ✔ FTE/partial FTE insourcing ✔ Project support ✔ Specialist consulting   Does your regulatory team need support? Let's connect! [email protected] #regulatoryaffairs #drugdevelopment #qualityassurance #pharmacovigilance #pharma #pharmaceuticals #biotech #marketaccess #pharmabusiness

Navigating a career in quality assurance within the pharmaceutical industry can be both challenging and rewarding. With stringent regulations and a constant pursuit of excellence, the path to success is paved with complexities. My expertise lies in guiding talents like you through these challenges, ensuring you're well-prepared to manage the intricacies of regulatory compliance. Let's connect and discuss tailored strategies to elevate your career in this dynamic field. #QualityAssurance #PharmaceuticalIndustry #CareerElevation

I'm on the look out for an experienced Quality Specialist, with 5 years Medical Device experience, and a Regulatory Manager with 5 years Medical Device and Pharmaceutical experience. Could you or anyone you know be interested? If you are intrigued and want more information about either of the opportunities listed below, pop me a message or email [email protected] and we can discuss further details. #hiring #medicaldevice #pharmaceutical #quality #regulatory #regulatoryaffairs #qualityassurance #pharmaceuticals

CAPA is the abbreviation for corrective and preventive actions. The term refers to the improvements to an organisation’s processes to mitigate undesirable situations like product nonconformities and is typically used in connection with quality assurance. CAPA can provide a structure for organisations to follow to find the cause of a problem, solve it, and identify ways to prevent the problem from occurring in the future. Thus, organisations correct the issue and prevent it going forward. Where To Utilise CAPA Principles? The CAPA method is relevant in multiple disciplines including: Manufacturing Product Design Testing Verification and Validation Distribution, Shipping, Transport, and Packaging The food processing, medical device development, and pharmaceutical industries are some of the industries in which CAPA is of particular importance. CAPA is also hugely important in the context of quality management. Certain quality control systems and standards require meticulous documentation of these processes. Phases In CAPA Adherence to an effective Corrective Action and Preventive Action process is essential in certain industries. It is a useful tool for companies to identify unconformities, resolve them, and prevent them from happening again. A good CAPA process consists of seven key phases. These include: 1:- Problem Identification and CAPA Initiation: In this phase, organisations will identify the problem at hand. The first step is to document the problem and describe it in as much detail as possible. 2:- Risk Evaluation: Performing a risk evaluation will help to identify the severity of the problem, which will determine the timeline for resolution. 3:- Investigation Procedure Preparation: Taking time to prepare the investigation procedure helps to know where to start and what to look for in the CAPA process. 4:- Root Cause Analysis : This step helps to identify exactly what caused the nonconformity. 5:- Corrective/Preventive Action Implementation: Next, organisations need to resolve the problem and implement measures to ensure that it won’t happen again in the future. 6:- Verification of Implementation and Effectiveness: After resolving the issue, it’s important to verify whether the solution works and is effective or not. If not, organisations will need to come up with a new solution. 7:- Closure and follow-ups: After verifying that the problem is resolved successfully and won’t happen again, the CAPA process can be closed. #capa #pharmaceutical #regulatorycompliance #pharmaupdates #regulatory #regulatoryaffairs #pharmaceutical

Navigating regulatory affairs in biopharma industry requires skilled talent pool: Expert

Koch Consulting provides experience in Project Management and Continuous improvement, Process optimization and CTPAT (USA)/ AEO (Europe). #pharma #lifesciences #consulting #quality #compliance #digitalbusinesstransformation #consultingexcellence #kochconsulting #Pharmaceutical #Pharma #PharmaProfessionals #Ad #hiring #careers #lifesciences #event #biotech #medicaldevice 

Does this sound familiar? A complex and demanding regulatory project just crash landed on your desk. Decisions must be made. Specialists need to be aligned. Deadlines must be met. For situations like this, we have brilliant experts to support you immediately. ·      Regulatory Project Manager ·      Global Regulatory Lead ·      Clinical Regulatory Expert ·      Regulatory CMC Expert ·      Labelling Specialist We offer flexible service models based on your needs: ·      FTE/partial FTE insourcing ·      Project support ·      Specialist consulting Does your regulatory team need support? Let's connect! [email protected] #regulatoryaffairs #drugdevelopment #qualityaffairs #pharmacovigilance #pharma #pharmaceuticals #biotech #marketaccess #pharmabusiness

Exploring the #Architectural Elegance of Model N in #Pharma Navigating complex #pricing, contracting, and #compliance landscapes in the dynamic world of pharmaceuticals can be daunting. Enter Model N’s #pharmaceutical architecture—a beacon of innovation and efficiency. Key Modules of #ModelN #Pharma: Revenue Management: Ensures compliance and optimizes revenue across diverse channels. #GovernmentPricing: Keeps up with ever-changing regulations, minimizing risks and ensuring transparency. #ContractManagement: Streamlines operations from negotiation to approval, enhancing agility and accuracy. The #integration of these modules within the Model N ecosystem provides pharmaceutical companies with a robust framework to manage revenues more effectively while staying compliant with regulatory demands. Calling all Pharma Model N #Architects and industry professionals! Let’s discuss how these technological advancements are shaping the future of #pharmaceuticals. How do you leverage Model N in your operations? #ModelN #PharmaIndustry #RevenueManagement #Compliance #ContractManagement #PharmaCareers #businessanalyst #opentowork #hiring #Gxp #LIMS #Datamapping #Agile #21cfr