NCH Corporation’s Post

Iam interested

Analytical chemist

Employers, how do you feel about cross-industry transferable skills? 🤔 In my sector, especially when dealing with analytical roles, I deal with candidates from a variety of backgrounds; Pharmaceutical, CRO's, Chemical Industry, Food industry, Environmental based labs etc. While almost all of these industries deal with different sampling and products, there can be lots of cross-over in the analytical equipment and lab processes used: 🧪 Candidates who have been in QC within the pharmaceutical industry may be trained in the likes of HPLC which can transfer over to Chemical-based CRO's carrying out characterization of incoming samples. 🧪 Candidates who have worked within the Waste industry may be trained in the likes of ICP- OES and MS which can transfer over into the precious metal industry. So my question is this... What is your stance on hiring candidates from other industries? Do you prefer to have the whole package that knows the industry? Or are you happy to nurture transferable skills and make them applicable to your industry? Let me know what you think in the comments... #TransferableSkills #AdaptableWorker #Employability

Good Opportunity

I think , the distribution of time during laboratory activities can be diffrent based analyst experience and preferences, also with factors like the complexity of test, number of steps , extent of manipulation . For example some tests can have an long test duration not due to manipulation but more due to numerous steps, such as drying time , injection time, shaking time, .. From my experience in the pharmaceutical industry, with GDP and GLP requirements, approximately 40 to 50% of the total time for documentation , data transcription and calculations needed to ensures clarity, reproducibility, transparency, and traceability of the analysis process and results. For regular analysis I would say: 1- 15% 2-40% 3-20%, 4-10%, 5-15 %

Attention laboratory chemists! We need your feedback for a case study aimed at enhancing the efficiency of laboratory analysis process. We want to identify the activities that consume the most time during the process. As a laboratory chemist, your input is invaluable to us. Please take a moment to estimate the percentage of time spent on each of the following activities during the analysis process: 1- Reflection on the Analytical Method 2- Method Execution 3- Documentation 4- Data Transcription 5- Calculation We would appreciate it if you could rate each option in the comment section. Unfortunately, LinkedIn does not provide poll options with rating functionality, but we hope to have this feature soon. Copy this in to the comment and change the percentages to reflect your experience 1- 20% ,2-20%, 3-20%, 4-20%, 5-20% Thank you for your cooperation. #laboratory #laboratorytechnician #laboratoryprofessionals #qc #pharma #continuousimprovement #lims #eln #quality

How do you choose the right formulation chemist for your project? I’ll give you 7 pillars: 1 - Expertise and specialization: Vet their track record and inquire about their experience in your industry or product category. 2 - Regulatory compliance: Ensure that the formulation chemist has a solid understanding of the regulatory requirements relevant to your product. 3 - Transparency and communication: Look for a formulation chemist who values transparency and maintains open contact lines. 4 - Portfolio and case studies: Review the chemist's portfolio and case studies to gauge the breadth and depth of their capabilities. 5 - Scalibility and flexibility: Can they handle projects of varying sizes, and are they adaptable to changes in project scope? 6 - Innovation and technology integration: Inquire about the formulation chemist's approach to innovation and whether they integrate cutting-edge technologies into their processes. 7 - Client references: Request client references or testimonials to gain insights into the experiences of previous clients. A reputable formulation chemist will gladly provide references. Hope this helps! P.S.: I turn people’s product concepts into cash 💰 DM me to create something of unparalleled value! #cosmeticchemist #productdevelopment #cleanbeauty #cosmetics #buildabrand

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QUALITY CONTROL LABORATORY COMPLIANCE-REFRESH Recommendations on setting the expiry period for commercial and in-house-prepared reagents used in the laboratories #Reagents are an integral part of any #laboratory and as such play a vital role in ensuring the validity of #analyticalresults. Reagents must be suitable for the intended use. Consideration should be given to the accompanying documentation and appropriate physico-chemical or biological #criticalqualityattributes for the intended purpose/s. In the laboratory, two major types of reagents are generally distinguished: #commercial and those prepared in the laboratory (#inhousereagents) using the former. It should be noted that the principles of #FIFO (First In-First Out) or #FEFO (First Expired-First Out) should be applied when using reagents. The #shelflife for an unopened product or #expiryperiod after first opening is usually set taking into account its #stability, i.e. how long the quality attributes and chemical integrity of the reagent can be maintained for the intended analytical application. This can be a challenging task because most manufacturers give the shelf life of the unopened product and do not provide information on how long the reagent is stable once the container has been opened. The recommendations for the shelf life of reagent solutions prepared and used in laboratories were established based on scientific data (including #validation data obtained from #qualitycontrolcharts, guidelines, standards, #pharmacopoeias, publications, etc.) and on the analytical experience and knowledge. Preparation times, costs, sustainable waste management policies and environmental protection concerns were also considered during the preparation of these recommendations. The recommendations on the shelf life of reagent solutions provided in the document should allow laboratories to assess whether a given solution can be used safely and reliably (provided that the #storageconditions comply with requirements) as they take into account various factors that contribute to the degradation of some reagents. For the purpose of this document, the expiry period of a reagent solution should be understood as the period of time during which the reagent is stable and can be used for a given type of analysis. ‼️It should be noted that the same reagent may be unfit for use for some purposes because it has expired, but still suitable for other purposes. Purchase or preparation of reagents and reagent solutions in quantities (volumes) not adapted to current needs should be avoided, as unnecessary disposal that does not take into account the possibility of prolonged use potentially constitutes a direct threat to the #environment. If prolonging the use of a reagent solution is safe and does not compromise the results, such prolongation should always be considered and justified. If you like this post follow me on LinkedIn #QC #compliance #reagents #testing #GLP #GMP

Department – Extraction Designation-DGM Experience – 15 to 20 Years Qualifications – B. Tech (Chemical) Department – Distillation Designation – DGM Experience – 15 to 20 Years Qualifications – B. Tech (Chemical) #hiring #vacancy #biotech #biotechjobs #pharma #opening #immediatehiring #pharmajobs #pharmacy #msc #biotechnology #research #project #lifescience #researchanddevelopment #drugdiscovery #openposition #clinical #scientist #biology #bioinformatics #jobopportunity