#sample sop for ms

[sopwritingexpert]

SOP for MS in Embedded Systems | Sample SOP Embedded Systems

🚀 Dreaming of a career in Embedded Systems?

Your SOP can open doors to top global universities!

Check out our latest blog on how to write an impactful SOP for MS in Embedded Systems, complete with tips, structure, and a sample to guide your journey.

📌 Tailored for future tech innovators like you!

Read now & start your journey toward admission success.

.

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[globlamanagergroup]

ISO 15189 Accreditation Documents: A Complete Documentation Kit

Achieving ISO 15189:2022 accreditation is essential for medical laboratories to demonstrate competence and ensure quality management compliance. To simplify this process, Global Manager Group offers a comprehensive ISO 15189 Documentation Kit, providing all necessary documents required for seamless accreditation.

What is ISO 15189:2022?

ISO 15189:2022 is the latest edition of the medical laboratory accreditation standard, aligned with ISO/IEC 17025. It introduces significant updates, including a stronger emphasis on risk management and incorporating requirements for Point of Care Testing (POCT) previously covered under ISO 22870.

Content of the ISO 15189 Documentation Kit

The ISO 15189 documentation kit consists of editable files, making documentation efficient and hassle-free. Key inclusions:

ISO 15189 Manual – Defines the implementation of the standard.

Quality Procedures – Covering various departments for a structured approach.

Standard Operating Procedures (SOPs) – Essential for collection, testing, and operational processes.

Exhibits – Guidelines for effective implementation.

Blank Forms & Templates – Ready-to-use formats for record-keeping.

Job Descriptions – Sample templates to define roles and responsibilities.

ISO 15189 Audit Checklist – Over 500 audit questions to assess compliance and improve efficiency.

Risk Assessment and Opportunity Sheet – A structured approach to managing laboratory risks.

ISO 15189:2022 Compliance Matrix – A reference guide for understanding documentation requirements.

Features of the Documentation Kit

Easy to edit – Provided in MS Word format (.docx) for quick customization.

User-friendly – Written in simple English for easy understanding and implementation.

Time-saving – Reduces document preparation efforts significantly.

Cost-effective – Provides value for money by minimizing documentation costs.

Audit-ready – Ensures laboratories are well-prepared for accreditation audits.

How This Kit Benefits Medical Laboratories

Helps laboratories achieve ISO 15189 accreditation efficiently.

Assists ISO 15189 consultants in guiding laboratories with pre-prepared templates.

Ensures compliance with risk-based approaches and quality requirements.

Saves time, effort, and cost in document preparation and training staff.

Get Your ISO 15189 Documentation Kit Today

For a seamless and structured approach to ISO 15189 accreditation, leverage the comprehensive ISO 15189 documentation kit by Global Manager Group. This kit ensures compliance, enhances laboratory efficiency, and simplifies the documentation process.

For more details, visit: Global Manager Group - ISO 15189 Accreditation Documents

[codician]

Billing / Invoice Automation using Google Sheets

Billing / Invoice Automation using Google Sheets

 ⭐️⭐️GITHUB

https://github.com/deepaklohia/google-sheets-billing-automation

⭐️GOOGLE SHEET SAMPLE

https://docs.google.com/spreadsheets/d/e/2PACX-1vSxUi1KfkWOINQlqagJX1ZFZy5FMFmMwxItVXuuHHZw8TpyvhFUxNY8KrDnd9yHMJ1r2Zjr-GWP1E8b/pubhtml

 ➡️ Google Sheets Fully Functional  Free Add-ons

⭐️Google Sheets Attendance Tracker

https://workspace.google.com/marketplace/app/attendance_tracker/602607637436

⭐️Google Sheets Time Tracker

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⭐️Google Sheets Combine Sheets

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⭐️Google Sheets TimeJet

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 ➡️OTHER USEFUL VBA AUTOMATIONS

how to extract notepad data in excel | VBA Automation

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 how to get Developer tab in MS Excel

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 How to run any exe file using VBA

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 Excel macro to convert pdf to excel

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 Attendance tracker (custom ribbon)

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 file inner text / content replacer - find and replace text

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 Excel Macro to convert pdf to Excel

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 how to merge excel files

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 how to track time and motion

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 send birthday greeting automatically

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 connect excel to word / create  letters in word automatically

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 how to remove password from MS Access database permanently

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 email domain name remover

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  google sheets, billing automation , customized billing, invoice , google app script , how to automate billing , invoice

[futuristictalefart]

Figure out how to organize a SOP for MS in software engineering from the actual specialists. Additionally, get tips and observe the normal slip-ups made by understudies.

[orthonathanganol]

Nathanael Warner

Brooklyn, NY, 11205                                        clevonwarner96@outlook.com 929-665-4506                  

__________________________________________________________________________________________________

SUMMARY:

Laboratory Technician with experience in device testing, food and drug testing and data analysis.

Research Assistant with experience in neuromodulation research & compound synthesis.

Seeking an intermediate position in an academic or industry laboratory.

__________________________________________________________________________________________________

EDUCATION:

Bachelor’s of Science, Chemistry, Howard University, 2019

Neuromodulation & Neuroimaging, UCLA, California, 2018

Associates Degree in Environmental Science, Presentation College, 2014

__________________________________________________________________________________________________

EXPERIENCE:

Title: Engineering Technician

Employer: Felix Storch Inc/Summit Appliances | 2022 - 2023

      770 Garrison Street, Bronx, NY 10474

~ Quality Assurance for Home and Medical Appliances

~ Ensured temperature compliance of refrigerators and freezers

~ Created reports on energy usage and efficiency.

~ Created labels for manufacturing and shipping departments.

~ Microsoft Access and Excel used for data and inventory management.

__________________________________________________________________________________________________

Title: Wearable Safety Technician

Employer: Google | 2020 – 2021

      40 Jessie Street, San Francisco, CA, 94105

<> Safety Testing for Smart Accessories 

<> Tested watch materials for the presence of skin irritants using GC/LC and ICP MS.

<> Created large volumes of artificial sweat, buffer solutions and solvents.

<> Performed lab maintenance tasks including ordering reagents and glassware.

<> Trained in lab’s safety, SOP, GDP and cGMP.

<> Python and Google Workspace used for data and inventory management.

__________________________________________________________________________________________________

Title: e-Commerce Shopper

Employer: Safeway Supermarket | Winter 2020 

    2020 Market St, San Francisco, CA 94114

Online Order Fulfillment

Completed online grocery orders for Safeway’s Drive Up and Go customers during COVID-19.

Able to work the frontend and backend of food retail environments.

Interacted directly with customers and worked with leadership to correct any problems.

Trained on inventory software for warehouse and retail.

__________________________________________________________________________________________________

Title: Food & Drugs Sample Technician

Employer: Element Materials Technology | 2019 – 2020

      9240 Santa Fe Springs Rd, Santa Fe Springs, CA, 90670

Heavy Metals Sample Testing

Prepared food and drug samples for heavy metals testing using ICPMS

Dissolved compounds via microwave superheating & acid/base digestions.

Tracked jobs, samples and reagents using 3rd party laboratory information management system.

Trained in lab’s safety, SOP, GDP and cGMP.

__________________________________________________________________________________________________

Title: Research Assistant

Employer: University of California, Los Angeles | 2018

    Semel Institute

    760 Westwood Plaza, Suite 57-430, Los Angeles, CA 90024

Spatial Navigation EEG Data in Humans

Spike sorted signals from electrodes implanted in the medial temporal lobes of patients being treated for epileptic seizures.

Identified theta modulations in brain wave activity during imagined activity as well as during real world movement.

EEG data analyzed using the wav_clus and MATLAB libraries for Python.

__________________________________________________________________________________________________

Title: Research Intern

Employer: Howard University | 2017 - 2019

    College of Pharmacy, 

    2201 Georgia Avenue, NW Washington, D.C. 20059

R&D for Turmeric Based Therapeutic Compounds 

Researched the curcumin molecule contained in turmeric.

Found that curcumin suppressed inflammatory responses in the brain and joints. 

Synthesized analogs of curcumin,  generally using Suzuki-Coupling mechanisms.

__________________________________________________________________________________________________

Title: Polymer Chemist

Employer: Global Marketing Enterprise | 2014 - 2015

   9 Fourth Street, Gasparillo, Trinidad and Tobago

Plastics Manufacturing 

Supervised recycling of plastics, transforming processed materials into pellets

Petrochemical research investigating environmentally safe methods to degrade polymers 

__________________________________________________________________________________________________

SKILLS

Formulations, microscopy, spectroscopy, separations, dilutions and other basic laboratory technique

Trained in cGMP, GLP and GDP

Computer programming - Python, HTML and some C++

Google Workspace & Microsoft Office

Fluent in French

[sudheervanguri]

 Dr. Reddy's Virtual Drive for Drug Substance, Bioassay, DQA, and Analytics. Are you a qualified professional looking to advance your career in biologics? Dr. Reddy's Laboratories is hosting a virtual drive exclusively for women on 9th June 2024. This event offers opportunities for various positions in Biologics, including Drug Substance, Bioassay, DQA, and Analytics. Join us virtually via MS Teams and take a significant step in your career. Read on for detailed information about job roles, qualifications, and how to apply. About Dr. Reddy's Laboratories Dr. Reddy's Laboratories is a global pharmaceutical company committed to providing affordable and innovative medicines. We value diversity and inclusion, and this virtual drive is part of our initiative to empower women in the workforce. Join our dynamic team and contribute to making a difference in global healthcare. Virtual Drive Details Date: 9th June 2024 Time: 9:30 AM onwards Mode: Virtual - MS Teams Location: Bachupally, Hyderabad Available Positions Drug Substance (2-8 years experience) Responsibilities: Handle downstream processes such as Chromatography, TFF Filtration Techniques, Aseptic Filtration, Buffer Preparation, and Column Packing. Knowledge and hands-on exposure to cell culture techniques, specifically in Bioassay (BA) Labs. Proficiency in software like Softmax Pro, PLA, LIMS. Qualifications: B Tech / MSc Bioassay (2-8 years experience) Responsibilities: Perform bioassay development and testing. Ensure precision and accuracy in all bioassay processes and documentation. Qualifications: Masters in Life Sciences / Biochemistry DQA (2-8 years experience) Responsibilities: Review and revise Standard Operating Procedures (SOPs). Oversee document control in product development and conduct risk assessments. Ensure data integrity and propose Quality by Design (QbD) process changes. Participate in phase gate reviews. Qualifications: Masters in Life Sciences / Biochemistry Analytics (2-8 years experience) Responsibilities: Conduct analysis of biosimilar products (drug substance, drug products, and in-process samples). Maintain lab safety, report discrepancies, and adhere to safety procedures. Qualifications: Masters in Life Sciences / Biochemistry How to Apply Interested candidates can register via the QR code or click the link below: Registration Link Why Join Dr. Reddy's Laboratories? At Dr. Reddy's Laboratories, we offer a supportive and inclusive work environment where employees can thrive. Our commitment to innovation, integrity, and excellence ensures that you will be part of a team dedicated to making a significant impact on global healthcare. We provide competitive salaries, excellent career development opportunities, and a culture that values diversity and inclusion. Note: This virtual drive is exclusively for women, encouraging diversity and inclusion within our workforce. [caption id="attachment_61190" align="aligncenter" width="930"] Dr. Reddys Recruitment Drive[/caption]

[lanettcdmo]

Navigating the Complex World of Analytical Development

Analytical development is a crucial aspect of pharmaceutical and biotechnology industries. It encompasses the processes and methodologies involved in developing reliable, accurate, and reproducible analytical methods to assess the quality, safety, and efficacy of drug substances and products. In this blog, we'll explore the key components of formulation analytical development, its importance, and the challenges faced by professionals in this field.

The Essence of Analytical Development

Analytical development is fundamental to the drug development process. It involves creating and validating analytical methods that are essential for:

Characterizing Active Pharmaceutical Ingredients (APIs): Understanding the chemical structure, purity, and potency of APIs.

Assessing Drug Products: Ensuring that the final drug products meet predefined specifications.

Quality Control: Monitoring the consistency and quality of drugs during manufacturing.

Regulatory Compliance: Meeting the stringent requirements set by regulatory bodies like the FDA and EMA.

Key Components of Analytical Development

Method Development:

Objective: Establish robust analytical methods to detect, quantify, and analyze the components of a pharmaceutical product.

Techniques: Various techniques like High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Mass Spectrometry (MS), and Nuclear Magnetic Resonance (NMR) are utilized.

Method Validation:

Purpose: Confirm that the analytical methods are reliable and produce consistent results.

Parameters: Accuracy, precision, specificity, sensitivity, reproducibility, and robustness are validated.

Stability Testing:

Goal: Determine how the quality of a drug substance or product varies with time under the influence of environmental factors such as temperature, humidity, and light.

Outcome: Provides data for establishing shelf life and storage conditions.

Regulatory Documentation:

Importance: Comprehensive documentation of the analytical methods and their validation is critical for regulatory submissions.

Content: Includes method development reports, validation protocols and reports, stability data, and standard operating procedures (SOPs).

Importance of Analytical Development

Ensuring Drug Safety and Efficacy

Analytical development ensures that drugs are safe for consumption and perform as intended. Accurate analytical methods help in detecting impurities, degradation products, and ensuring that the active ingredient is present in the correct dosage.

Supporting Drug Approval and Market Access

Regulatory agencies require detailed analytical data to approve new drugs. Robust analytical methods and thorough validation are essential for gaining regulatory approval and bringing new drugs to market.

Enhancing Manufacturing Quality

During the manufacturing process, consistent analytical methods are vital for quality control. They help in monitoring the production process, ensuring that each batch of drug meets the required standards.

Facilitating Research and Development

In R&D, analytical methods are used to study the pharmacokinetics, bioavailability, and metabolic pathways of new drugs. This information is crucial for optimizing drug formulations and dosing regimens.

Challenges in Analytical Development

Rapid Technological Advancements

Keeping pace with rapid advancements in analytical technologies can be challenging. Continuous learning and adaptation are required to incorporate new techniques and instruments into existing workflows.

Regulatory Compliance

Navigating the complex regulatory landscape is a significant challenge. Each regulatory agency may have different requirements, and staying compliant requires meticulous attention to detail and thorough documentation.

Sample Complexity

Pharmaceutical samples can be highly complex, containing multiple components and potential impurities. Developing methods that can accurately analyze such complex matrices is often difficult.

Resource Constraints

Analytical development requires significant resources, including skilled personnel, sophisticated instruments, and adequate funding. Balancing these resources efficiently is crucial for timely and successful method development.

Future Trends in Analytical Development

Integration of Artificial Intelligence and Machine Learning

AI and ML are increasingly being integrated into analytical development to enhance method development, optimize processes, and predict outcomes. These technologies can significantly reduce development time and improve accuracy.

Automation and High-Throughput Screening

Automation and high-throughput screening are revolutionizing analytical development. They allow for faster and more efficient analysis of large numbers of samples, accelerating the drug development process.

Advanced Analytical Techniques

Emerging techniques such as Ultra-High-Performance Liquid Chromatography (UHPLC), tandem mass spectrometry (MS/MS), and next-generation sequencing (NGS) are pushing the boundaries of what is possible in analytical development.

Conclusion

Analytical development is a cornerstone of the pharmaceutical and biotechnology industries, ensuring that drugs are safe, effective, and of high quality. While it presents several challenges, the integration of advanced technologies and continuous innovation hold great promise for the future. As the field evolves, staying abreast of new developments and maintaining rigorous standards will be key to success in this critical area of drug development.

[mbafromgermany]

SOP for Germany — Sample, Tips & Format for German Universities

Statement of Purpose (SOP) plays a pivotal role in your application process when seeking admission to German universities. It serves as a platform to convey your academic journey, career aspirations, and reasons for choosing a particular program. In this blog post, we'll delve into the essentials of crafting a compelling SOP for German universities, offering a sample, useful tips, and the appropriate format.

Recommended: Scholarships in Germany for Indian Students  

Understanding the Importance of SOP for German Universities:

German universities place significant importance on the SOP as part of their selection process. It offers insights into your personality, motivation, and suitability for the program. A well-crafted SOP can distinguish you from other applicants and enhance your chances of acceptance.

Sample SOP for Germany:

[Note: This is a hypothetical sample SOP for illustrative purposes only.]

Name: [Your Name]

Program Applied for: Master of Science in Mechanical Engineering

Introduction:

My name is [Your Name], and I am writing this statement of purpose to express my keen interest in pursuing a Master of Science in Mechanical Engineering in Germany. With a robust academic background and a fervent passion for engineering, I am excited about the opportunity to further my education in one of Europe's leading technical domains.

Academic Background:

I completed my Bachelor's degree in Mechanical Engineering with distinction. Throughout my undergraduate journey, I acquired a solid understanding of mechanical principles and gained practical experience through internships and projects. My coursework equipped me with skills in thermodynamics, fluid mechanics, and solid mechanics.

Research and Extracurricular Activities:

During my undergraduate tenure, I actively engaged in research projects focused on renewable energy systems and sustainability. Collaborating with peers and professors, I contributed to projects aimed at optimizing the performance of wind turbines and solar panels. These experiences ignited my passion for sustainable engineering and spurred my desire to delve deeper into the field.

Career Goals and Alignment with Program:

My long-term aspiration is to become a leader in sustainable engineering, driving innovation to combat environmental challenges. The Master of Science in Mechanical Engineering program in Germany offers a comprehensive curriculum with a focus on sustainability and renewable energy. Modules such as "Advanced Topics in Renewable Energy" resonate with my academic and career objectives, providing me with the necessary skills to effect positive change in the industry.

Recommended: MS in lightweight Engineering in Germany  

Why Germany:

I am drawn to Germany for its renowned engineering education and research opportunities. The country's commitment to technological advancement and innovation aligns with my career aspirations. Additionally, studying in Germany will expose me to diverse perspectives and foster a global outlook, which are essential qualities for success in today's interconnected world.

Recommended: Study in Germany for Indian Students  

Tips for Writing an Effective SOP for Germany:

Begin Early: Start drafting your SOP well in advance to allow ample time for revisions.

Be Authentic: Showcase your genuine passion and motivations for pursuing the program.

Customize: Tailor your SOP to each university and program to demonstrate your specific interest.

Highlight Achievements: Emphasize relevant academic accomplishments, research experience, and extracurricular activities.

Clarity and Conciseness: Keep your writing clear, concise, and free of unnecessary jargon.

Proofread: Review your SOP multiple times for grammar, spelling, and punctuation errors.

Recommended: MS in Germany   

Format for SOP:

Introduction: Introduce yourself and state your purpose.

Academic Background: Provide an overview of your academic journey.

Research and Extracurricular Activities: Discuss relevant experiences and projects.

Career Goals: Articulate your aspirations and how the program aligns with them.

Why Germany: Explain your motivation for studying in Germany.

Conclusion: Summarize your key points and reiterate your enthusiasm.

Recommended: Scholarships in Germany for Indian Students  

Conclusion:

Crafting an effective SOP is essential for securing admission to German universities. Following the tips outlined in this blog post and adhering to the appropriate format, you can effectively convey your academic journey, aspirations, and passion for your chosen field of study. Good luck with your application!

[mycollectionzzz]

Where To Find Ideal Sample SOPs For MS In CS?

There is a saying. Make hay while the sun shines. What it implies is that one must be ready and prepared to take advantage of the opportunities that are currently available to him. When one tries to understand it in the context of career and advanced studies, there are many programmes there which guarantee jobs upon completion. One must choose to study the best course in order to land a rewarding job in the field. Master’s programme in computer science is one of them. You should apply for the course in the best institution with the best sample SOPs for MS in CS.

Where to find the best sample SOPs for MS in CS?

If you are looking for the ideal sample statement of purpose for MS in CS, your search ends here. Being the best professional SOP writers, we have helped hundreds of students in securing admission in higher education institutions abroad with the help of suitable admission essays.

Request us for a sample SOP for MS in computer science with work experience or without.

[onlinemachaindia]

Grade Average Calculator - OnlineMacha

Check your academic score that it is equivalent to a German grade, OnlineMacha.com gives you the most accurate and fastest way, where you fill your CGPA and get the result in a second. Our grade average calculator is free, simple, and easy to use. Visit now.

[globlamanagergroup]

ISO 20121 Documents for Event Sustainability Certification

Global Manager Group offers a complete suite of ISO 20121:2024 documents, including the ESMS (Event Sustainability Management System) manual, procedures, SOPs, policies, audit checklists, and sample templates.

Achieving ISO 20121:2024 certification for sustainable event management requires clear, comprehensive, and easy-to-implement documentation. Global Manager Group offers a complete suite of ISO 20121:2024 documents, including the ESMS (Event Sustainability Management System) manual, procedures, SOPs, policies, audit checklists, and sample templates.

Key Features of Our ISO 20121:2024 Documentation Kit: User-Friendly Language: Documents are written in simple English for easy understanding and implementation.

Editable Formats: Available in .docx, .xlsx, and .pptx formats, compatible with MS Office 2007 and newer versions.

Comprehensive Coverage: Includes a fully editable ESMS manual, procedures, work instructions, SOPs, audit checklists, and templates that align with ISO 20121:2024 requirements.

Customizable: Easily tailor the documents to your specific organizational needs, ensuring they meet the unique demands of your events.

Developed by Experts: The documentation is created by a team with years of experience in ISO certification, having completed over 200 projects globally.

Time-Saving: Ready-made templates and documents help you save valuable time during the certification process, ensuring a quicker route to ISO 20121:2024 compliance.

Why Choose Global Manager Group?

Global Manager Group's ISO 20121:2024 documents are developed under the guidance of experienced ISO consultants and sustainability experts, ensuring that all documents comply with the latest standards. This documentation model provides a simple, efficient way to meet the sustainability goals of your event management system without excessive paperwork. Whether you're organizing a small corporate gathering or a large international conference, our templates and resources are adaptable to various event sizes and requirements.

By using our kit, you not only save time but also gain better control over your event sustainability management. Our templates, including work instructions and SOPs, allow you to streamline processes, minimize environmental impact, and enhance your organization's social responsibility efforts. This complete and customizable solution ensures that your organization stays aligned with ISO 20121:2024 requirements, driving sustainable practices in every event you host.

For more details, visit Global Manager Group.

[statementervices]

Seeking admission abroad for MS in Computer Science program? Good Choice of career. However, there are some procedures that you have to follow while seeking admission in the program of your choice. You have to draft an SOP for procuring admission to the university of your choice. You have heard of the proficient SOP writers… But you have not assessed their writings. You have an option to seek the services of best SOP writers. Peruse the SOP Samples For MS in Computer Science before you confirm the choice of writers.

[orthonathanganol]

Nathanael Warner

Brooklyn, NY, 11205                                        clevonwarner96@outlook.com 929-665-4506                  

__________________________________________________________________________________________________

SUMMARY:

Laboratory Technician with experience in device testing, food and drug testing and data analysis.

Research Assistant with experience in neuromodulation research & compound synthesis.

Seeking an intermediate position in an academic or industry laboratory.

__________________________________________________________________________________________________

EDUCATION:

Bachelor’s of Science, Chemistry, Howard University, 2019

Neuromodulation & Neuroimaging, UCLA, California, 2018

Associates Degree in Environmental Science, Presentation College, 2014

__________________________________________________________________________________________________

EXPERIENCE:

Title: Engineering Technician

Employer: Felix Storch Inc/Summit Appliances | 2022 - 2023

      770 Garrison Street, Bronx, NY 10474

Quality Assurance for Home and Medical Appliances

Ensured temperature compliance of refrigerators and freezers

Created reports on energy usage and efficiency.

Created labels for manufacturing and shipping departments.

Microsoft Access and Excel used for data and inventory management.

__________________________________________________________________________________________________

Title: Wearable Safety Technician

Employer: Google | 2020 – 2021

      40 Jessie Street, San Francisco, CA, 94105

Safety Testing for Smart Accessories 

Tested watch materials for the presence of skin irritants using GC/LC and ICP MS.

Created large volumes of artificial sweat, buffer solutions and solvents.

Performed lab maintenance tasks including ordering reagents and glassware.

Trained in lab’s safety, SOP, GDP and cGMP.

Python and Google Workspace used for data and inventory management.

__________________________________________________________________________________________________

Title: e-Commerce Shopper

Employer: Safeway Supermarket | Winter 2020 

    2020 Market St, San Francisco, CA 94114

Online Order Fulfillment

Completed online grocery orders for Safeway’s Drive Up and Go customers during COVID-19.

Able to work the frontend and backend of food retail environments.

Interacted directly with customers and worked with leadership to correct any problems.

Trained on inventory software for warehouse and retail.

__________________________________________________________________________________________________

Title: Food & Drugs Sample Technician

Employer: Element Materials Technology | 2019 – 2020

      9240 Santa Fe Springs Rd, Santa Fe Springs, CA, 90670

Heavy Metals Sample Testing

Prepared food and drug samples for heavy metals testing using ICPMS

Dissolved compounds via microwave superheating & acid/base digestions.

Tracked jobs, samples and reagents using 3rd party laboratory information management system.

Trained in lab’s safety, SOP, GDP and cGMP.

__________________________________________________________________________________________________

Title: Research Assistant

Employer: University of California, Los Angeles | 2018

    Semel Institute

    760 Westwood Plaza, Suite 57-430, Los Angeles, CA 90024

Spatial Navigation EEG Data in Humans

Spike sorted signals from electrodes implanted in the medial temporal lobes of patients being treated for epileptic seizures.

Identified theta modulations in brain wave activity during imagined activity as well as during real world movement.

EEG data analyzed using the wav_clus and MATLAB libraries for Python.

__________________________________________________________________________________________________

Title: Research Intern

Employer: Howard University | 2017 - 2019

    College of Pharmacy, 

    2201 Georgia Avenue, NW Washington, D.C. 20059

R&D for Turmeric Based Therapeutic Compounds 

Researched the curcumin molecule contained in turmeric.

Found that curcumin suppressed inflammatory responses in the brain and joints. 

Synthesized analogs of curcumin,  generally using Suzuki-Coupling mechanisms.

__________________________________________________________________________________________________

Title: Polymer Chemist

Employer: Global Marketing Enterprise | 2014 - 2015

   9 Fourth Street, Gasparillo, Trinidad and Tobago

Plastics Manufacturing 

Supervised recycling of plastics, transforming processed materials into pellets

Petrochemical research investigating environmentally safe methods to degrade polymers 

__________________________________________________________________________________________________

SKILLS

Formulations, microscopy, spectroscopy, separations, dilutions and other basic laboratory technique

Trained in cGMP, GLP and GDP

Computer programming - Python, HTML and some C++

Google Workspace & Microsoft Office

Fluent in French

[profileevaluationtool]

https://profileevaluation.com/sample-sop-for-ms-in-computer-science/

[lanettcdmo]

Navigating the Complex World of Analytical Development

Analytical development is a crucial aspect of pharmaceutical and biotechnology industries. It encompasses the processes and methodologies involved in developing reliable, accurate, and reproducible analytical methods to assess the quality, safety, and efficacy of drug substances and products. In this blog, we'll explore the key components of formulation analytical development, its importance, and the challenges faced by professionals in this field.

The Essence of Analytical Development

Analytical development is fundamental to the drug development process. It involves creating and validating analytical methods that are essential for:

Characterizing Active Pharmaceutical Ingredients (APIs): Understanding the chemical structure, purity, and potency of APIs.

Assessing Drug Products: Ensuring that the final drug products meet predefined specifications.

Quality Control: Monitoring the consistency and quality of drugs during manufacturing.

Regulatory Compliance: Meeting the stringent requirements set by regulatory bodies like the FDA and EMA.

Key Components of Analytical Development

Method Development:

Objective: Establish robust analytical methods to detect, quantify, and analyze the components of a pharmaceutical product.

Techniques: Various techniques like High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Mass Spectrometry (MS), and Nuclear Magnetic Resonance (NMR) are utilized.

Method Validation:

Purpose: Confirm that the analytical methods are reliable and produce consistent results.

Parameters: Accuracy, precision, specificity, sensitivity, reproducibility, and robustness are validated.

Stability Testing:

Goal: Determine how the quality of a drug substance or product varies with time under the influence of environmental factors such as temperature, humidity, and light.

Outcome: Provides data for establishing shelf life and storage conditions.

Regulatory Documentation:

Importance: Comprehensive documentation of the analytical methods and their validation is critical for regulatory submissions.

Content: Includes method development reports, validation protocols and reports, stability data, and standard operating procedures (SOPs).

Importance of Analytical Development

Ensuring Drug Safety and Efficacy

Analytical development ensures that drugs are safe for consumption and perform as intended. Accurate analytical methods help in detecting impurities, degradation products, and ensuring that the active ingredient is present in the correct dosage.

Supporting Drug Approval and Market Access

Regulatory agencies require detailed analytical data to approve new drugs. Robust analytical methods and thorough validation are essential for gaining regulatory approval and bringing new drugs to market.

Enhancing Manufacturing Quality

During the manufacturing process, consistent analytical methods are vital for quality control. They help in monitoring the production process, ensuring that each batch of drug meets the required standards.

Facilitating Research and Development

In R&D, analytical methods are used to study the pharmacokinetics, bioavailability, and metabolic pathways of new drugs. This information is crucial for optimizing drug formulations and dosing regimens.

Challenges in Analytical Development

Rapid Technological Advancements

Keeping pace with rapid advancements in analytical technologies can be challenging. Continuous learning and adaptation are required to incorporate new techniques and instruments into existing workflows.

Regulatory Compliance

Navigating the complex regulatory landscape is a significant challenge. Each regulatory agency may have different requirements, and staying compliant requires meticulous attention to detail and thorough documentation.

Sample Complexity

Pharmaceutical samples can be highly complex, containing multiple components and potential impurities. Developing methods that can accurately analyze such complex matrices is often difficult.

Resource Constraints

Analytical development requires significant resources, including skilled personnel, sophisticated instruments, and adequate funding. Balancing these resources efficiently is crucial for timely and successful method development.

Future Trends in Analytical Development

Integration of Artificial Intelligence and Machine Learning

AI and ML are increasingly being integrated into analytical development to enhance method development, optimize processes, and predict outcomes. These technologies can significantly reduce development time and improve accuracy.

Automation and High-Throughput Screening

Automation and high-throughput screening are revolutionizing analytical development. They allow for faster and more efficient analysis of large numbers of samples, accelerating the drug development process.

Advanced Analytical Techniques

Emerging techniques such as Ultra-High-Performance Liquid Chromatography (UHPLC), tandem mass spectrometry (MS/MS), and next-generation sequencing (NGS) are pushing the boundaries of what is possible in analytical development.

Conclusion

Analytical development is a cornerstone of the pharmaceutical and biotechnology industries, ensuring that drugs are safe, effective, and of high quality. While it presents several challenges, the integration of advanced technologies and continuous innovation hold great promise for the future. As the field evolves, staying abreast of new developments and maintaining rigorous standards will be key to success in this critical area of drug development.