Hire the best Regulatory Compliance Freelancers in Pakistan

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$50 hourly
Akmal Y.
- 5.0/5
- (23 jobs)
Hi, Akmal is a cosmetic formulator working as a cosmetic chemist for 5 years. He can do ingredient research, sourcing of ingredients, formulation of ingredients, and finally, can run a test batch (optional) for your cosmetic product including skincare, haircare, and makeup while complying with required guidelines such as Vegan, Natural, Sephora clean, and Credo clean. You would get your fully prepared personal care product at a one-stop shop according to your need such as organic or synthetic products. If you want something innovative, just give him a try! What can you get? ✅Cosmetic Ingredient Research: He would select the ingredients from scientific studies to make sure the efficiency of the cosmetic product. He would cross the safety of the ingredients from different sources such as EWG and Drug bank to make sure the safety of the cosmetic product. ✅Cosmetic Ingredient Sourcing: You will get the most authentic and economical suppliers who don’t have large minimum orders. If any selected ingredient is hard to be sourced, you will get an alternative ingredient or formulation method to synthesize in the lab. ✅Cosmetic Ingredient Formulation: You would get the function of each ingredient along with effective concentration, so you may understand your product. You would get a scalable format of cosmetic formulation, so you may produce batch size according to your choice. You would get the manufacturing guideline and required equipment, so you may know what would be needed. They would also provide you with final product properties such as texture, pH and shelf life, so you may know what would it look like. ✅Test Batch: You can tell him to run a test batch for your personal care product. Their lab is in the USA.

Regulatory Compliance
Organic & Natural Style
Reverse Engineering
Chemical Engineering
Skin Care
Cosmetics
Cosmetic Regulation
Label Compliance
Product Development
Product Formulation
Cosmetic Raw Materials
Biochemistry
Chemical Synthesis
Research & Development
$40 hourly
Azam A.
- 5.0/5
- (57 jobs)
An experienced tax accountant, IRS authorized tax preparer, Certifying Acceptance Agent (CAA) and business consultant specialized in ITIN obtention, LLC formation, tax preparation, sales tax license, resale permit, and sales report filing. Accomplished 300+ projects with 100% customer satisfaction. Have portfolio of over 80 foreign owned LLCs for tax return preparation and sales tax report filing in PA, TX, WY, FL and OK. I am experienced in LLC formation, EIN, ITIN, U.S taxation of Foreign owned LLCs, reporting requirements and LLCs obligations. Based on my in-depth knowledge, skill set and experience, I can serve your business needs. My expertise is: - - ITIN obtention - US LLC formation & annual compliance with State & FINCEN - EIN obtainment - LLC Tax forms preparation of US Non-Residents (SMLLC + MMLLCs+ NR personal taxes - Sales Tax License - LLC's Sales Tax report filing with Sates - Accomplishments - LLC formation + EIN+ITIN - Prepared tax return of over 80 foreign owned US LLCs - Delivered 300+ projects (Related to business formation, Tax issues) - 30+ Companies incorporated in Pakistan - 55+LLC formed in Wyoming, Delaware, Texas and Florida - Monthly Sales Tax filing of 20 LLCs - 25+ITIN obtained - 100% customer satisfaction Top quality work and Customer satisfaction has always been my TOP Priority.

Regulatory Compliance
Amazon Listing
Compliance Consultation
Corporate Tax
Tax Law Compliance
Limited Liability Company
Amazon PPC
Amazon FBA
Tax Preparation
Tax Preparation Software
Sales Tax
Value-Added Tax
Tax Planning & Advisory
Tax Return
$15 hourly
Muhammad Akmal S.
- 4.9/5
- (228 jobs)
🏆 Top Rated, Senior Legal Consultant and Advisor. 🏆 +7 years of professional experience. 🏆 Former Associate (Freelance) Attorney to a Pennsylvania Based Law Firm. 🏆 More than 1000 happy clients as a Freelance Lawyer. I am a highly skilled and experienced lawyer with a proven track record of providing top-notch legal services to clients worldwide. With over 7 years of experience in the legal field, I offer a comprehensive range of legal solutions tailored to meet my clients' specific needs. With a rich and diverse client base encompassing individuals, Pro Se litigants, LLCs, Enterprises, Corporations, Partnerships, Sole Proprietorships, Trusts, Charities, and Multinational Companies, I have had the privilege of working on a wide range of legal cases and intricate legal problems. I will never disappoint you while choosing me in your legal issues. Proficiencies: ✅Contract Law: I specialize in reviewing, drafting, and negotiating contracts to protect your rights and interests. Whether it's business contracts, employment agreements, Intellectual Property License Agreements or lease agreements, I ensure clarity and enforceability. ✅Civil Law: You can fully trust my expertise in litigation regarding, real estate, rent, leases, breach of contracts, frauds etc. I will draft compelling legal demand letters, lawsuit complaints, motions, replies, discovery requests and provide complete legal consultation. ✅Intellectual Property: I provide expert advice on trademarks, copyrights, patents, and trade secrets, helping you secure and defend your IP rights. My cease and desist letters have proved very effective and I have assisted numerous clients in their Amazon, eBay, Walmart, Etsy store issues/litigation. ✅Personal Injury Law: To have an experienced legal consultant in Personal Injury claims is not less than a blessing. With my in-depth understanding and proven track record in Personal Injury claims, I will walk you through your claim. ✅Employment Law: Navigating the complexities of employment law is vital for both employers and employees. I provide guidance on matters such as workplace policies, discrimination claims, employee contracts, and termination issues. ✅Business and Corporate Law: From business formation and compliance to mergers and acquisitions, I offer comprehensive legal support to businesses of all sizes. I assist with contract disputes, partnership agreements, corporate governance, and more. ✅Legal Research and Writing: I possess excellent research skills and can provide in-depth legal analysis and well-crafted written content. Whether it's legal memos, briefs, or opinions, I deliver high-quality work that is persuasive and comprehensive. By choosing my services, you can expect: 🥇Diligent attention to detail and meticulous research. 🥇Clear and effective communication throughout the project. 🥇Timely delivery of high-quality work. 🥇Exceptional results with reliable, and cost-effective legal assistance. Let's work together to overcome legal hurdles and achieve your goals. Feel free to reach out to me to discuss your specific legal requirements. I am excited to collaborate with you and provide the legal expertise you need to succeed. God Bless.

Regulatory Compliance
Intellectual Property Consulting
Legal Consulting
Legal Agreement
Patent Law
Employment Law
Criminal Law
Family Law
Intellectual Property Law
Civil Law
Trademark Consulting
Legal Drafting
Legal Writing
Contract Drafting
Legal Research
$30 hourly
Muhammad A.
- 4.7/5
- (102 jobs)
Are you looking for a Health, Safety, and Environmental expert who can transform your workplace into a compliant, safe, and productive environment? Or perhaps you need a technical writer to simplify complex topics for your audience? If so, I might just be the right consultant for you. I know it sounds bold, but give me a moment to explain. My name is Muhammad Arif, and I am a seasoned Health, Safety & Environmental (HSE) consultant with a unique blend of expertise in Product Safety, Compliance, and Technical Writing. I’ve helped businesses across various industries create safer workplaces, reduce risks, and navigate complex regulations. Plus, I’ve been helping companies break down complex safety and regulatory materials into clear, concise documents for their teams and stakeholders. Now, I’m not just your average consultant or writer. With over 15 years of experience, I’ve worked with global companies, ensuring they meet OSHA, ISO, API, and other industry standards. My track record speaks for itself, and I’m confident I can deliver results tailored to your specific needs. Here’s what one of my clients had to say: "Muhammad helped us streamline our safety procedures, cutting compliance issues in half and making our workplace safer than ever. His expertise is invaluable." When it comes to HSE and product safety, the gravest mistake that many consultants make is offering cookie-cutter solutions or simply checking off boxes. Let’s be honest, compliance might look good on paper, but it’s not effective unless it’s genuinely preventing incidents and protecting your business. As a technical writer, I also understand how important it is to communicate complex HSE regulations and safety protocols in a way that is easily understood by your team. I specialize in creating clear, actionable documents like SOPs, safety manuals, and compliance reports, ensuring that even the most complicated concepts are conveyed simply and effectively. That’s where I come in. I focus on more than just meeting regulations—I dive deep into your unique challenges, whether it’s preventing workplace accidents, managing environmental risks, or ensuring product safety. I understand that true safety is proactive, not reactive. Working on hundreds of diverse projects has given me the experience to handle complex safety and compliance issues across multiple industries. Whether you’re in manufacturing, construction, oil & gas, or any other field, I’ve likely worked on similar challenges. And that’s why, if you decide to work with me, the process will be seamless, frustration-free, and results-driven. But here’s the catch: I don’t take on every project. I prioritize clients who are committed to improving their safety culture and who understand the importance of compliance in protecting their workforce and business. So, if you're ready to take your safety and compliance efforts to the next level, reduce risks, and ensure long-term success… Click the button above to contact me, and let’s discuss how I can help make your workplace safer, more compliant, and your documentation clear and impactful. Your Next HSE Consultant & Technical Writer, Muhammad Arif

Regulatory Compliance
Copywriting
Research & Development
Compliance Consultation
Technical Writing
Quality, Health, Safety & Environment Management
$25 hourly
Naveed A.
- 5.0/5
- (11 jobs)
I am a QMS and Regulatory Affairs Expert with over 20 years of professional experience in the medical devices industry. Some of my other specialties include technical writing, including Quality Manual (QM), Standard Operating Procedures (SOPs), Quality Plans, Quality Forms, and other QMS document writing and review for medical device companies and any other business complying with ISO standards such as ISO 9001, ISO 13485, ISO 14001, and SA 8000, among others. I have extensive experience in developing technical files and other necessary documentation in compliance with MDR 2017/745 and MDD 93/42/EEC. Additionally, I can assist you well with the following: • Registration of Economic Operators and Products with EUDAMED • Clinical Evaluation Report • Post Market Surveillance Reports • Risk Management in compliance with ISO 14971 (FMEA, FMECA, etc.) • Incident Response Plan and Report • Audit Preparations/Compliances (USFDA, MHRA, ISO 9001, ISO 13485, ISO 14001, SA 8000) Finally, I am an expert in quality management systems (QMS) for medical devices. I have helped numerous companies implement QMS processes that are compliant with ISO 13485, FDA QSR, and other relevant regulations. I am well-versed in the design, implementation, and maintenance of QMS processes, and can help companies ensure that their QMS is robust and effective. If you are looking for a regulatory affairs consultant, medical device content writer, or QMS expert, I would be delighted to help. Please get in touch to discuss your needs and how I can assist you in achieving your goals. Prepare technical file documentation and quality system documents of medical devices Class I, Class IIa, and Class IIb for compliance with EU MDR 2017/745. Create QMS to ISO 13485:2016 processes and procedures. I have prepared technical documentation for regulatory submission globally Following Documents will be Provided under MDR and FDA in my service plan Declaration of Conformity Design & Manufacturing Information General Safety & Performance Requirements Harmonized Standard Compliance Risk Management Plan Risk Management Report Verification & Validation Report Post Market Surveillance Packaging & Labelling CER Plan. Undertaking. Technical File Summary CER (Clinical Evaluation) BER (Biological Evaluation) IFU EUDAMED REGISTRATION PROCESS As part of the EUDAMED registration process, you will also need to register the details of the person who is acting as the PRRC (Annex VI, Part A 1.4), including their name and address. REGISTER WITH FDA I would also be happy to assist you in developing the dossier and its submission with FDA, USA, in compliance with 510(K), as well as registering your company and device listing with the FDA. This includes: • Submitting the Establishment Registration. • Preparing and submitting the Device Listing. • Updating any changes to the Establishment Registration (e.g., address, change in ownership, etc.) • Notifying the FDA of changes in telephone, fax, or email address to keep lines of communication open. HEALTH CANADA (CMDR) MEDICAL DEVICE REGISTRATION AND APPROVAL In Canada, you must obtain a Medical Device Establishment License (MDEL) if you intend to market your Class I device, or a Medical Device License (MDL) for your Class II, III, or IV device. If you want to distribute licensed medical devices in Canada, you will require an MDEL. Your MDL or MDEL application must be in full compliance with the CMDR and be submitted to Health Canada in conjunction with the appropriate documentation required for your device class. I would also be happy to assist you in submission with Health Canada, in compliance with CMDR, as well as registering your company and device listing with Health Canada. This includes: • Review & analyze the client’s device information • Apply & interpret Health Canada classification rules, applicable to the client devices • Recommend a preliminary device classification to Health Canada • Respond to Health Canada questions • Facilitate a formal classification ruling for medical devices directly from Health Canada • Report back to the client • Address any client questions

Regulatory Compliance
Legal
Virtual Assistance
Amazon FBA
Medical Device User Manual
Good Manufacturing Practice
Literature Review
Drawing
ISO 9001
Risk Management
Internal Auditing
Medical Device
Quality Management System
Procedure Development
Technical Documentation
$10 hourly
Shahmeer A.
- 5.0/5
- (4 jobs)
I am an experienced corporate commercial lawyer educated from King's College London (UK) and Columbia University (US) and qualified from Pakistan with over eight years of experience of representing big & small corporations on a wide range of legal matters. I provide a diverse set of legal services to clients across the globe at affordable prices including contract management (including contracts drafting, review, redlining, abstraction & summarization), as well as legal drafting services (such as memos, case summaries and briefs), para legal and legal support services. I handle projects on fixed fee basis as well on hourly basis, depending upon the requirement of the client and my rates vary depending upon the nature and complexity of the project. Having worked with three of the leading Pakistani law firms – Cornelius, Lane & Mufti, Raja Mohammad Akram & Co and HaidermotaBNR&Co. in the past, I have now founded a law firm called "Khan & Arshad" and am independently working primarily with national and international clients on a variety of projects. My practice covers diverse areas of corporate commercial law including M&A, joint ventures , start up advisory, real estate transactions, energy projects and tax matters and I have extensive knowledge and experience in drafting and review of commercial contracts for clients worldwide including Confidentiality/Non-Disclosure Agreements, Memorandum of Understandings (MoUs), Shareholders' Agreement, Share Purchase Agreements, Joint Venture Agreements, variety of Service Agreements including Master Services Agreements, Terms and Conditions and Privacy Policy of websites, Employment Agreements, Consultancy Agreements, Procurement Agreements, IT Agreements, Rent/Lease/Sale Agreements for property, Technical Licensing/Collaboration Agreement, contracts related to purchase and lease of land/ buildings. I possess excellent communication skills, common law knowledge and the requisite skill set to provide the right and superior quality legal and paralegal support services for any jurisdiction (including USA, Australia, UK and Asia). I am not qualified to advise on local laws of foreign jurisdiction (i.e., other than India) but render variety of legal advise based on common law principles. I use plain English to communicate verbally and in my documentation. I am extremely responsive and committed to deliver highest levels of quality services within the agreed timelines. I can fully assure you of complete data integrity, confidentiality and conflicts of interest.

Regulatory Compliance
Compliance
Legal Consulting
Trade Law
Commercial Litigation
Legal Agreement
Corporate Governance
Due Diligence
Corporate Law
Contract Law
Litigation
Contract Drafting
Real Estate
$25 hourly
Faisal N.
- 4.8/5
- (20 jobs)
Hi, I am a skilled & experienced "Food & Supplements Consultant & ( US FDA, USDA, EU, UK/FSA, Canada/CFIA & FSANZ Specialist) Regulatory Compliance Expert for import and export of the Food & Supplements products in USA, UK, Canada, Europe, China, India & any other country. Experience & Qualifications: 🏆 Top Rated Food & Supplements Consultant | ( US FDA, USDA EU, UK/FSA, Canada/CFIA & FSANZ) Regulatory Compliance Specialist 🏆 100% Job Success Score as FDA Compliance Specialist for Amazon/Shopify & Import vs Export 🏆 05+ years of Experience as a Professional Assistant Manager (Quality Assurance) & Food Safety Auditor/ Food Safety Officer/ Food Safety & Quality Specialist 🏆 Graduate Degree in "Food Science & Technology" & Post-graduation degree in "Food Safety & Quality standards Control" What I Offer: ✅ Regulatory Compliance for Supplements | 21 CFR 111/117, HACCP, FSMS" & Food Safety ✅ Nutraceutical and food supplement formulation and regulatory compliance. ✅ FDA (21 CFR 111 & 117), FSVP, FSMA, ISO, FSSC 22000, and other global standards, ✅ Top-tier safety, compliance, and quality. ✅ HACCP plan development, food safety audits, label reviews, FDA registration, and import/export compliance for dietary supplements, food products, and cosmetics. ✅ HAZARD ANALYSIS AND CRITICAL CONTROL POINT (HACCP) ✅ 21 CFR part 111- CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS ✅ 21 CFR 117-CURRENT GOOD MANUFACTURING PRACTICE, HAZARD ANALYSIS, AND RISK-BASED PREVENTIVE CONTROLS FOR HUMAN FOOD. - PCQI - FSPCA Preventive Controls for Human Foods - Food Label Review - Nutrition Labeling/Food Labels/FDA Labeling including Canadian CFIA Bilingual Nutrition - Product Labels (Food or Supplements or other) - Food product labels and Nutritional Values - Labeling compliance: Ingredients list, Allergens, Nutrition panels, Product common name etc... - Product specification - SOP’s/Policies for, SQF, Halal, Kosher, Organic, Non-GMO - SOP's/Documents/Audit Reports - Quality Food Safety policies & Procedures - Development of Supplier Management System/Pre-Qualification Questionnaires - FSVP Foreign Supplier Verification Program

Regulatory Compliance
Quality Audit
Quality Assurance
Total Quality Management
Microbiology
Animals & Pets
Factory & Supplier Auditing
HR & Business Services
Label Compliance
Food Science
Food & Beverage
Retail & Consumer Goods
Good Manufacturing Practice
USDA
Food & Supplements
$30 hourly
Zia U.
- 5.0/5
- (5 jobs)
With seven years of regulatory affairs experience in the pharmaceutical and cosmetic industries, I specialize in guiding companies through complex regulatory processes to achieve market authorization and compliance. My expertise includes: • Pharmaceutical Submissions: Successfully submitted ANDAs to the US-FDA, generic hybrid applications to the EU and MHRA, and managed compliance audits for API and excipient manufacturing per ICH Q7. • End-to-End Project Leadership: Led projects from product development to market authorization, including drafting, reviewing, and submitting M1, M2, and M3 dossiers via E-CTD, ensuring gap analysis to avoid refuse-to-receipt (RTR). • Regional Expertise (Module 1): Prepared and submitted regional information for FDA, EU, and MHRA, including filling out FDA forms (e.g., 356h, 2253) and drafting compliance declarations. • Pre-ANDA Consultations: Provided pre-submission support, including FDA communications, Q1/Q2 sameness assessments, and threshold analysis. • Cosmetic Compliance: Assisted cosmetic manufacturers in registering firms and products with the FDA under MOCRA regulations, ensuring full compliance. • Technical & CMC Writing: Developed high-quality technical and CMC documentation, including SOPs, audit reports, and API sourcing evaluations. • Supplier Management: Sourced active pharmaceutical ingredients (APIs), managed supplier relationships, and finalized audit reports to ensure compliance and quality standards. I bring a proven track record of delivering successful submissions, maintaining regulatory compliance, and streamlining processes to help companies navigate complex requirements efficiently. I am here to: • Provide guidance regarding your NDA, ANDA and IND • Provide complete strategy for your submission • Register your drug and cosmetic facility • Register your cosmetic product per FDA MOCRA regulation • Help in drafting the documentation for MAA (Marketing authorization application) for drug products • Review your drug product package and do gap analysis to avoid RTR (Refuse to review) • Review all your pdf documents per FDA and EU regulation • Optimize and validate all your pdf documentation for eCTD submission and publishing • Sourcing API (Active pharmaceutical ingredients) supplier • Helping in the documentation and supplier management • Writing DMF (Drug master file) and doing gap analysis • Provide consultation regarding CMC (Chemistry, manufacturing and control) • Help fill out all FDA forms per FDA regulations I can do many other related tasks; just ask! Thank you for taking the time to review my profile. My 100% success score on Upwork reflects my commitment to delivering results right the first time. If I don’t meet your expectations, I’ll work for free until you’re happy and fully satisfied. I look forward to connecting and supporting your regulatory needs.

Regulatory Compliance
Biotechnology Regulation
Quality Management System
Supplier Development
Quality Assurance
Quality Control
Scientific Research
Supplier Search
Product Label
Technical Writing
Cosmetics
Research & Development
Product Development
Writing
Drug Regulation
$10 hourly
Yusra S.
- 5.0/5
- (15 jobs)
As an Amazon Hazmat Consultant, I create Safety Data Sheets (SDS) and Amazon Hazmat Exemption Sheets, which enable Amazon Sellers to successfully complete Amazon Hazmat review process (Dangerous Goods Program).. I'm a Chemical Engineering Graduate with over 4 years experience in Technical Writing (in Chemical and Processing field) which includes writing research articles, reports, handling safety systems, and solving complex designing problems. I'm currently providing my services as a Safety Data Sheet (SDS) Author and Amazon Consultant with an expertise in solving Hazmat issues. Whether you're trying to * Overcome challenges of Amazon Hazmat * Clear Export/ Import customs * Or you need SDS for any other purpose You can feel free to contact me because * I possess a considerable knowledge and experience of writing and revising GHS and Amazon Complaint Safety Data Sheets (SDS) and Amazon Hazmat Exemption Sheet. * From gathering data to hazard analysis, I'm well equipped to handle a range of technical challenges. * I offer a full time support * I have more than 4 years freelancing experience in the field with 100% positive client feedback. I am willing to guide you with the best of my knowledge and abilities. Your satisfaction is my ultimate aim.

Regulatory Compliance
Data Collection
Process Flow Diagram
Process Engineering
Process Design
Technical Writing
Process Safety
Process Documentation
Chemical Engineering
Amazon FBA Product Research
Workplace Safety & Health
Amazon Listing
Amazon Product Research
Data Sheet Writing
Safety Assessment
$10 hourly
Muhammad K.
- 5.0/5
- (44 jobs)
Certified Cosmetic Safety Assessor with extensive experience in preparing CPSRs (Cosmetic Product Safety Reports), PIFs (Product Information Files), SDSs (Safety Data Sheets), and Cosmetic Product Notifications for EU/UK compliance. I specialize in helping cosmetic brands, startups, and manufacturers meet regulatory standards while ensuring product safety, quality, and market readiness. My expertise also includes creating custom formulations tailored to your needs, including natural, vegan, and cruelty-free products. Whether you need allergen analysis, cosmetic compliance documents, or unique product development, I provide accurate, reliable, and timely solutions to support your success in competitive markets. Let’s collaborate to bring your cosmetic products to life and ensure they meet global compliance standards!

Regulatory Compliance
Toxicology
Product Development
Safety Assessment
Process Improvement
Chemical Engineering
Quality Assurance
Cosmetic Regulation
Chemistry
Cosmetics
Cosmetic Raw Materials
$35 hourly
Uzair K.
- 5.0/5
- (4 jobs)
I have more than nine years of banking experience, during which I have worked in Anti-Money Laundering (AML), Policies & Procedures, Regulatory Compliance, Risk Assessment, Process Improvement & Reengineering Departments. In my diversify experience, I have learnt and excelled in many skills, which includes: - Client review in terms of AML, Regulatory Instruction and internal Policies. - Identification of Risk, including AML, Regulatory Instruction and internal Policies. - Evaluate the screening results against the client in respect of AML, Sanctions, PEP, and other relevant risks - Document formation & standardization and review of bank’s policies & procedures, user manual, training materials, internal forms, Service Level Agreement and business requirement & specification document. - Advisory and guidance to internal stakeholders on compliance, regulatory matters, and internal policies & procedures. - Training to internal stakeholders on Regulatory Instructions and Internal policies & procedures. - Identifying different business processes for improving, revamping, or completely reengineering the identified process. - Analyze the existing “AS IS” process through different techniques and methods, including documentation gap, customer complaints, bottleneck, revenue generation and cost-saving. - Conduct joint sessions with relevant stakeholders while applying best practices to create and document the future “TO BE” process and attain stakeholders and approvals. - How to conduct User Acceptance Testing (UAT) and resolve the issues identified before go-live. Academically, I have done a master's in Economics and I am ACCA Member.

Regulatory Compliance
Company Policy
Process Design
Process Improvement
User Manual
Microsoft Visio
Policy Writing
Procedure Manual
Anti-Money Laundering
Business Process Management
Risk Assessment
Process Documentation
Process Flow Diagram
Business Process Reengineering
Business Analysis
$35 hourly
Nauman A.
- 5.0/5
- (3 jobs)
Goods reaches the destination - smoothly, makes me and client happy. With masters in Logistics & Supply Chain Management, and 3 years of professional experience in global logistics (US imports), I try my best while coordinating with all concerned parties (consignees, shipping lines, truckers, warehouses, overseas agents etc.) to deliver the cargo timely. Excellent command in all US import operations starting from shipment starts, ISF filing, client vendor communication, customs clearance, FDA compliances (expertise in cosmetics and medical devices), delivery arrangements, POD handling and lastly, billing (making sure no one gets late payment) - hence a one window operation! Sit back and let me help your cargo reach the destination, without hustle!

Regulatory Compliance
Import Procedure
Logistics Management
Logistics Coordination
Data Entry
Tariff Classification
Warehouse Management
Document Review
Supply Chain & Logistics
Client Management
Transportation & Warehousing
Price & Quote Negotiation
Third-Party Logistics
Customer Relationship Management
Customer Service
$60 hourly
Rizwan A.
- 4.5/5
- (19 jobs)
Strong ability to excel in a project team environment, More than 15 year of experience in applying the principles and theories of Food science & Engineering helping to invent and improve products and processes have set up & operated. Monitored experiments, made observations and record results; keep detailed logs for all work assignments; performed manufacturing processes and ensured quality by testing products for proper proportions of ingredients, for purity, and for strength. Specialties: Project Management. Product & Packaging Development Process Improvement Food Laws & Product registration. Analysis & Evaluation of the food Product. (Physical, Chemical & Microbiological). Product Command 1. Nutritional & health Supplements (Powder & Syrups) 2. Confectionery (Candies, Gummies, Lollypop, Toffies) 3. Baked Products (Biscuits, Muffin & Cakes) 4. Premixes ( Baking, Coating, breading) 5. Beverages (RTD & Stimulant) 6. Spices, Seasonings & Rubs 7. Snacks (Fried, Baked & Extruded) 8. Condiments My forte and the favorite thing is label compliance review! I can review your device, OTC drug, supplement, food, and cosmetic labels for compliance to US FDA, EU Directives, Health Canada, and more! Food Regulations (FDA / USDA, EU, FSANZ, CFIA, GCC FOOD LAWS, UK FOOD STANDARDS AGENCY

Regulatory Compliance
Food Engineering
Biology Consultation
Nutrition
Chemistry
Food & Supplements
Industrial Product
Good Manufacturing Practice
Recipe Development
Product Formulation
Process Development
Product Development
Research & Development
Consumer Goods
$44 hourly
Duaa S.
- 5.0/5
- (15 jobs)
⭐Honored to Work as a Ghostwriter for McKinsey, Forbes & Bloomberg 🤩 #1st Certified Pakistani Freelance Writer, Researcher & Kalviyo Expert 🏆 Working w/ The World's Best Top-Selling Authors 💰 $260M+ Generated In Sales & Funding ⏱️ 1750+ Working Hours Completed Bringing Your Vision to Life... 🌟 It’s not just about finding a freelancer—it’s about finding someone as committed to your success as you are. With over 6 years of experience and more than 300 projects under my hands, your vision has become my mission. Whether it’s expert writing, insightful research, or strategic planning, you’re in the right place to see real results. Grant Proposals That Get Funded... 💰 Securing funding is critical, and you need someone to make your grant proposal stand out. With a proven track record of winning grants, I’ll help you craft submissions that catch attention and get approved. Let’s secure the funding you need to bring your vision to life. Strategies That Propel Your Business Forward... 🚀 Your business deserves more than cookie-cutter strategies. I deliver tailored business plans, market analyses, and growth strategies that align perfectly with your goals. This isn’t just about planning—it’s about creating actionable strategies that drive real growth. Content That Connects and Converts... 💬 Your audience deserves content that speaks directly to them. From compelling sales copy to engaging blog posts, I create content that not only resonates but also drives action. Let’s make your message impossible to ignore. Research That Informs and Empowers... 🔎 Good decisions come from solid research. I dive deep into market trends, competitor analysis, and more to provide you with clear, actionable insights. With this information at your fingertips, you’ll be ready to make decisions that set you apart from the competition. Your Goals, My Commitment... 💪 When we work together, your goals become my goals. I’m not just here to complete a project—I’m here to ensure that what we achieve together makes a lasting impact. Your success is the priority, and I’m committed to making it happen. Ready to Make a Real Impact? 🎯 Success isn’t a matter of chance—it’s a matter of making the right moves. Click the "INVITE" or "HIRE" button, and let’s start a conversation that will take your business to the next level. Let’s make your goals a reality, together.

Regulatory Compliance
Medical Device
Drug Regulation
Technical Writing
Blog Writing
Ad Copy
Sales Copy
Copywriting
Research & Development
Product Research
Quantitative Analysis
SEO Writing
Qualitative Research
Market Analysis
Market Research
$75 hourly
M Amir A.
- 5.0/5
- (7 jobs)
I am a licensed lawyer, working for top law firms. I have served over 284+ clients all over the world in corporate and other different sectors. Providing; |Legal Consultancy| |Legal Advice| |Contract Review| |Procedural Guidance| |Disputes Consultancy| |Litigation Review| |Legal Drafting| |Legal Agreement| |Amazon Dispute Settlement| |Amazon Account Reactivation| |Amazon Appeals| |FDA Consultation| |FDA Registrations| |LLC Documents| |Privacy Policies| |Terms and conditions| |Plaints| |Written Statements| |Motions| |Complaints| |Documents Review| I have immense experience in the U.S, and U.K Common Law Systems, and the Civil Law Systems of European countries. Get in touch today.

Regulatory Compliance
ADR
Alternative Dispute Resolution
Compliance
Drug Regulation
Real Estate Law
Personal Injury Law
Privacy Policy Writing
Intellectual Property Law
Civil Law
Legal Applications & Registration
Legal Consulting
Litigation
Contract Law
Corporate Law
$44 hourly
Syed S.
- 4.9/5
- (99 jobs)
FDA & FMCG Compliance expert (Top Rated Plus - Among top 3% on Upwork) and Food Industry enthusiast with 9+ years of experience in various food industries in Quality Assurance & Compliance department. I'm a certified PCQI and an FSVP and Lead Auditor for BRCGS Food Safety Issue:9 & ISO FSSC 22000. Services I specialize at: - Foreign Supplier Verification Program (FSVP) - Food/Supplement Label Review - FDA Domestic & Foreign Food Facility Registration + Certificate + US Agent Service - FSVP & IOR Agent Service - FDA Import Alert Removal from Red List and DWPE (Detention Without Physical Examination) - FSSC 22000, ISO:22000, BRCGS & Food Safety Management System Implementation - Food Safety Plan/ Amazon Food Safety Plan Development - FDA, CFIA, EU, UK, FSANZ Compliant Nutritional Panels Development (including Bilingual Nutrition Panels) - Supplement Facts Development - HACCP Plan Development - Hazard Analysis & Risk Assessment - Nutrition Labeling/Food Labels/FDA Labeling - Cosmetics Products Formulation (Organic & Vegan) - GMO's/Bioengineered Foods/Genetically Modifying Organisms - SOP’s/Policies for BRCGS, FSSC 22000, ISO:22000, QMS:9001, IFS, SQF, Halal, Kosher, Organic, Non-GMO, FDA regulations - SOP's/Documents/Audit Reports Translation (Spanish/French/German to English) - Quality Food Safety & HSE policies & Procedures - Systems certifications FSSC, BRCGS, IFS, SQF, QMS:9001 - Food Science & Food Technologist Queries - COA's (Certificate of Analysis) - Development of Supplier Management System/Pre-Qualification Questionnaire - Corporate Social Responsibility (CSR Labor & Human Rights, Ethics, Environmental, Health & Safety, Workplace Diversity, Sustainability) Procedures/Policies Development. Standards & Certifications: BRCGS Food Safety Issue:9, FSSC 22000, ISO:22000, Ecovadis, HACCP, ISO QMS:9001, Non-GMO, Organic EU & Organic NOP, cGMP, IFS, SQF, GMP+FSA, Kosher, Halal & FDA registration. Feel free to contact for consultation services, systems implementation, FSVP/FSMA/FSSC 22000/FDA compliance. Just a message away to offer my services. Feel free to contact for any query in detail. #FSVP #FSMA #HACCP #PCQI #LABELREVIEW #FDA #FDACOMPLIANCE #FSSC #FSSC22000 #ISO9001 #QMS9001 #BRCGS #IFS #NONGMO #ECOVADIS #FSVP #GMP #cGMP #IMPORTALERT #UPWORK #FMCG #FOOD #FDA #NUTRITIONFACTS #NUTRITIONPANEL

Regulatory Compliance
Food Packaging
Label & Packaging Design
Label Compliance
Food Writing
Food Science
Food & Supplements
Quality, Health, Safety & Environment Management
ISO 9001
Food & Beverage
Procedure Development
Quality Management System
Chemistry
Compliance Consultation
Risk Assessment
$35 hourly
Muhammad Asim K.
- 5.0/5
- (1 job)
I'm an ISO Management System consultant with a passion for helping businesses thrive. With over 27 years of experience and a track record of certifying over 350 companies worldwide, I can help you develop, implement, and refine your ISO systems to achieve excellence. Here's what I bring to the table: Clear and concise documentation: Manuals, policies, procedures – I'll make sure your team has everything they need to succeed. Seamless internal audits: We'll work together to identify any gaps and ensure your systems are running smoothly. Proactive risk management: Let's mitigate risks before they become problems. ISO certification support: Get that official stamp of approval and showcase your commitment to quality. Ready to take your business to the next level? Let's chat! Lead Auditor & Areas of Expertise: ✅ ISO 9001:2015 Quality Management System (QMS) ✅ ISO 14001:2015 Environmental Management System (EMS) ✅ ISO 45001:2018 Occupational Health & Safety (OHS) ✅ ISO 27001:2022 Information Security & Cyber Security (ISMS) ✅ ISO 20000-1 Service Management System (SMS) ✅ ISO 22301:2019 Business Continuity Management System (BCMS) ✅ ISO 17025:2017 Laboratory Management System (LMS) ✅ ISO 22000:2018 Food Safety Management System (FSMS) & HACCP ✅ ISO 50001:2018 Energy Management System (EnMS) ✅ ISO 13485:2016 Medical Devices QMS ✅ Occupational Safety & Health Administration (OSHA) regulations ✅ cGMP & FDA 21 CFR Part 820 & 111 ✅ CE Marking ✅ Eco-label ✅ Oeko-Tex 100 ✅ FDA ✅ Halal/Kosher ✅ BSCI/BRC ✅ CSR/SA 8000 Moreover, I bring extensive experience as a Textiles Engineer from the UK and a Project Management expert, driving profitability, sustainable growth, operational efficiency, and innovation in diverse industries.

Regulatory Compliance
Food Science
Label Compliance
Compliance Consultation
Textile Engineering
Factory & Supplier Auditing
Risk Management
Sustainability
Quality Audit
Technical Documentation
Quality, Health, Safety & Environment Management
Certified Information Systems Security Professional
ISO/IEC 20000
ISO 27001
ISO 9001
$30 hourly
Shayan A.
- 5.0/5
- (23 jobs)
I am vastly experienced in providing third party consultation to ensure compliance of management systems to standards like ISO 9001, ISO 27001, ISO 20000, ISO 14001, ISO 17025, ISO 17001, OSHAS 18000, etc. and Formulating of documentation and SOPs to fulfill standard requirements along with research into modern management and production standards.

Regulatory Compliance
Project Risk Management
Manufacturing & Construction
Internal Auditing
ISO 27001
ISO/IEC 20000
Risk Assessment
ISO 14001
Management Consulting
ISO 9001
Occupational Health
Business Consulting
ISO 9000
Documentation
$15 hourly
Hamid H.
- 5.0/5
- (10 jobs)
I'm a results-oriented management professional who has led health, safety, quality, and environmental compliance management for highly reputable international companies. I've a contagious enthusiasm and passion for compliance management. I've 11+ years of experience working with globally distributed teams for organisations of all sizes to create, inspire, implement, and innovate compliance management systems. My servant-leadership approach, coupled with pragmatic stakeholder engagement, lends itself to working in the construction, manufacturing, information security, transport & aviation, logistics & cargo, homecare, adult & childcare, cement manufacturing, and cybersecurity industries. Hamid has gained recognition by clients and peers for establishing successful and scalable compliance environments through people, processes, and culture. I'm also results-driven, self-motivated, an accelerator, and an incubator. I work with businesses, institutions, start-ups, and organisations to provide compliance management, environmental consultancy, documentation, administrative support, and ISO certification assurance. As a freelancer, I have been working on multiple environmental, health, safety, and sustainability projects in a variety of industries across Europe, the UK, UAE, USA, Canada, Australia, Singapore, and more. My key areas of expertise include but not limited to: - Compliance management for OSHA, CCOHS Canada, HSE UK, WorkSafeBC, Safe Work AU, - Environmental Health and Safety Management - Disaster risk management, vulnerability assessment - Developing effective prevention, mitigation, and adaptation measures - Auditing for Quality, Health, Safety, and Environmental management - Occupational health & safety management and planning - Developing workplace sustainability policies, procedures, and recommendations - Emergency preparedness, management, and communication - Hazardous material management and control, utilization, and contamination prevention International industry standards development implementation, maintenance, and auditing: ✅ ISO 14001 (Environmental Management) ✅ISO 45001 (Occupational Health and Safety) ✅ISO 9001 (Quality Management) ✅ISO 27001 (information Security Management System)

Regulatory Compliance
Procedure Manual
Environmental, Health & Safety Software
AIMS Chameleon
Quality Management System
Project Risk Management
Quality, Health, Safety & Environment Management
Safety Engineering
Workplace Safety & Health
Process Safety
ISO 14001
Compliance Consultation
ISO 9001
Quality Audit
Manufacturing & Construction
$10 hourly
Muhammad Haris M.
- 5.0/5
- (1 job)
Results-driven professional with a unique combination of financial, immigration, and investment expertise. As a Senior Financial Analyst, I have been responsible for preparation of Net worth, financial statements and financial analysis. Further, I have successfully guided individuals through the complex immigration process. Additionally, my experience as a Stock Analyst has equipped me with a deep understanding of financial markets, investment strategies, and risk management. Services Offered: - Financial analysis - Bookkeeping - Immigration consulting and case management - Investment research and portfolio management - Financial reporting Expertise: - Financial Analysis - Immigration Consulting (investor and entrepreneur applications of Canada & USA) - Stock Analysis and Investment Research - Financial Modeling and Forecasting - Financial Reporting and Compliance - Investment Strategy and Portfolio Management - Risk Management and Mitigation Tools and Technologies: - Financial software (Excel, Quick books, Xero, fox pro, tally, Kordeva CRM) Education and Certifications: - ACCA - B.COM Language Skills: - English - Urdu

Regulatory Compliance
Technical Analysis
Immigration
Financial Reporting
Bookkeeping
Financial Analysis
Financial Accounting
$15 hourly
Kashif N.
- 5.0/5
- (2 jobs)
I am a highly skilled and experienced Food & Supplements Consultant specializing in cGMP, HACCP, FDA regulatory compliance, and label standards. I offer expert consultation on selecting dietary ingredients to formulate effective and visually appealing supplements that build confidence in both consumers and manufacturers. Additionally, I ensure that ingredients, labels, COAs, cGMP, HACCP, ISO certifications, marketing strategies, and health/structure claims or new dietary claims comply with FDA, FSA, CFIA, UK, and EU regulations. With my assistance, you can successfully launch your food and supplement products on platforms like Amazon, eBay, Etsy, or Alibaba. Services: ◉ Dietary supplement formulations & label compliance (FDA/USDA, EU, FSA, CFIA, FSANZ) ◉ Ingredient sourcing, manufacturing, warehousing, and distribution ◉ HACCP plans for restaurants, mobile carts, catering, and retail ◉ GMP compliance (21 CFR 117 for food, 21 CFR 111 for dietary supplements) ◉ Writing and implementing food safety programs ◉ FDA food facility & cosmetic product registration and labeling ◉ Specialized expertise in organic, herbal, and nutritional supplements (e.g., weight loss, fitness, probiotics) Services I specialize at: - Foreign Supplier Verification Program (FSVP) - Food/Supplement Label Review - FDA Domestic & Foreign Food Facility Registration + Certificate + US Agent Service - FSVP & IOR Agent Service - FDA Import Alert Removal from Red List and DWPE (Detention Without Physical Examination) - FSSC 22000, ISO:22000, BRCGS & Food Safety Management System Implementation - Food Safety Plan/ Amazon Food Safety Plan Development - FDA, CFIA, EU, UK, FSANZ Compliant Nutritional Panels Development (including Bilingual Nutrition Panels) - Supplement Facts Panel - HACCP Plan/ HARPC/PCP - Hazard Analysis & Risk Assessment - Nutrition Labeling/Food Labels/FDA Labeling - Cosmetics Products Formulation (Organic & Vegan) - GMO's/Bioengineered Foods/Genetically Modifying Organisms - SOP’s/Policies for BRCGS, FSSC 22000, ISO:22000, QMS:9001, IFS, SQF, Halal, Kosher, Organic, Non-GMO, FDA regulations - SOP's/Documents/Audit Reports Translation (Spanish/French/German to English) - Quality Food Safety & HSE policies & Procedures - Systems certifications FSSC, BRCGS, IFS, SQF, QMS:9001 - Food Science & Food Technologist Queries - COA's (Certificate of Analysis) - Development of Supplier Management System/Pre-Qualification Questionnaire - Corporate Social Responsibility (CSR Labor & Human Rights, Ethics, Environmental, Health & Safety, Workplace Diversity, Sustainability) Procedures/Policies Development. Standards & Certifications: BRCGS Food Safety Issue:9, FSSC 22000, ISO:22000, Ecovadis, HACCP, ISO QMS:9001, Non-GMO, Organic EU & Organic NOP, cGMP, IFS, SQF, GMP+FSA, Kosher, Halal & FDA registration. Feel free to contact for consultation services, systems implementation, FSVP/FSMA/FSSC 22000/FDA compliance. Just a message away to offer my services. Feel free to contact for any query in detail. #FSVP #FSMA #HACCP #PCQI #LABELREVIEW #FDA #FDACOMPLIANCE #FSSC #FSSC22000 #ISO9001 #QMS9001 #BRCGS #IFS #NONGMO #ECOVADIS #FSVP #GMP #cGMP #IMPORTALERT #UPWORK #FMCG #FOOD #FDA #NUTRITIONFACTS #NUTRITIONPANEL Let’s connect to simplify compliance and grow your business!

Regulatory Compliance
Ecommerce Development Consultation
Food & Beverage
Product Label
Label Compliance
Label & Packaging Design
Private Labeling & White Labeling
Cosmetic Regulation
Defense Federal Acquisition Regulation Supplement
Food Science
Food Engineering
Product Development
Nutrition
Recipe Development
Food & Supplements
$11 hourly
Syed Naveed S.
- 4.9/5
- (4 jobs)
I am an experienced medical credentialing specialist with 2 years of hands-on experience managing healthcare provider credentialing, ensuring compliance with insurance requirements, and facilitating smooth reimbursement processes. My role centers around verifying credentials, maintaining accurate provider records, and collaborating with insurance companies and healthcare providers to meet industry regulations. With a strong focus on attention to detail, effective communication, and time management, I work diligently to ensure healthcare providers are credentialed and re-credentialed on time, enabling seamless claims processing. Key Skills: - Credentialing & Privileging: Extensive experience verifying and managing provider credentials and privileges. - Regulatory Compliance: Deep knowledge of state and federal regulations governing healthcare credentialing. - Verification Processes: Expertise in primary source verification, background checks, and handling credentialing documentation. - Data Management: Skilled in managing provider databases and safeguarding sensitive information. - Insurance Enrollment: Proficient with major insurance payers, including Medicare, Medicaid, and commercial insurance plans. - Documentation & Reporting: Preparing credential files, generating reports, and ensuring accurate documentation. - Communication: Strong ability to liaise with healthcare providers, insurance companies, and internal teams. Experience: In my previous role, I successfully managed the credentialing process for over 100 healthcare providers, ensuring timely application submissions and renewals. Through this, I was able to reduce processing time by 50%, significantly improving efficiency and regulatory compliance. Tools & Software: Credentialing Software: Advanced user of CAQH, NPPES, and Availity. Database Management: Proficient in MS Excel and Access. Document Management Systems: Experienced with SharePoint and DocuSign for document handling and electronic signatures. Why Choose Me: I’m committed to providing top-notch credentialing services with a focus on accuracy, efficiency, and regulatory compliance. With my proactive approach and keen attention to detail, you can rest assured that your credentialing needs will be handled with the utmost professionalism and care. If you're looking for a credentialing specialist who values efficiency and accuracy, let's connect and streamline your process! Regards Naveed

Regulatory Compliance
Contract Negotiation
HIPAA
Virtual Assistance
Insurance Verification
Data Entry
Customer Service
Administrative Support
Problem Solving
Communications
Project Management
$40 hourly
Umair A.
- 4.2/5
- (7 jobs)
Regulatory affair consultant: Hi, Myself ''Engr. Umair '' I am an experienced Scientist and Engineer working in some Major fields of following: 1. Biomedical Engineering 2. Biomedical Science 3. Medical Educational Experience: I am a MEDICAL Engineer and have done multiple research projects: 1. Public health research, including epidemiology. 2. Kidney diseases 3. CPAP Now working as BIOMEDICAL Researcher, technical writer and regulatory consultant. I have provided strategic support in regulatory affairs, post-market product surveillance, and quality assurance in CE marking of EU Class I, IIa, IIb or III medical devices by writing Clinical Evaluation Reports (CERs) providing clinical evidence of the device's state of the art for medical treatment and its safety and performance and response to notified body feedback. If you want your device CE marked, and you want to have a certification on MEDDEV 2.7.1 Rev.4 as well as on MDR, then you are in the right place. I have extensively Experienced in MDR-medical device regulation and FDA regulations for medical devices and drugs. I have provided strategic support in regulatory affairs, post-market product surveillance, and quality assurance in CE marking of EU Class I, IIa, IIb or III medical devices by writing Clinical Evaluation Reports (CER's) providing clinical evidence of the device's state of the art for medical treatment and its safety and performance and response to notified body feedback. Technical Experience: • Over 6+ years of Regulatory Affairs experience in Medical Devices Industry. Exceptional Scientific and Technical skills in Regulatory Affairs, Quality Assurance. • Good written, verbal and interpersonal communication skills, decision-making and problem-solving. • Work efficiently under pressure, multitasks in a timely manner, excellent collaboration when working with others on various projects and a fast learner. • Experience with global regulatory strategy and worldwide submissions. • Experience with quality systems development- authored SOPs, performed gap analysis per FDA QSR 820, ISO 13485:2016. • Experience with ISO 14971:2019 about risk Management of medical devices. • Knowledge of FDA Quality System Regulations 21 CFR 820, and 821, 21 CFR 801, 21 CFR 812, 21 CFR 814, EU Medical Device Regulation (MDR), and applicable guidance documents. • Knowledge of Medical Device Design Controls, and product life cycle management, as well as applicable standards. • Knowledge and Submission of IVD medical devices. • Support the maintenance of Technical File, Device History Record (DHR), Device Master Record (DMR), and Design History File (DHF). • Organize and maintain data generated from new product testing. • Well organized and self-motivated with a drive for excellence offering high-quality analytical work in a timely manner. • Excellent verbal and communication skills • Able to analyze, negotiate and solve problems quickly, to achieve individual and team goals. • Enjoy learning new skills with a desire for continuous personal growth, reliable, hardworking team player with ability to adapt to new situations. ISO Standars on that I have worked on: • ISO 13484:2016 • ISO 14971:2019 • ISO 10993-1:2021 • IEC 60601 • IEC 62304 • EU MDR 2017/745 • 21 CFR 820.198 • FDA 21 CFR Part 820 Quality System Regulations • 21 CFR Part 11 Electronic Records • cGXP (GLP, GMP) I have created Multiple Technical Documentation according to MEDDEV 2.7.1 Rev.4 and then updated it to MDR (EU) 2017/745. The following Documents will be Provided under MDR in my service plan Declaration of Conformity Design & Manufacturing Information General Safety & Performance Requirements Harmonized Standard Compliance Risk Management Plan Risk Management Report Verification & Validation Report Post Market Surveillance Packaging & Labelling CER Plan. Undertaking. Technical File Summary CER (Clinical Evaluation) BER (Biological Evaluation) IFU

Regulatory Compliance
Medical Device
Biomedical Engineering
Medical Device User Manual
Proofreading
Technical Documentation Management
Food & Supplements
Technical Documentation
Technical Writing
$20 hourly
Mirza Ali B.
- 5.0/5
- (0 jobs)
As a dedicated ACCA and CFCS qualified professional with more than 1o years of experience in internal audit, compliance, risk management, and governance, I bring a wealth of experience from my tenure in Commercial, Microfinance and Islamic banks, as well as fintechs. My specialization in fintech and digital banking equips me with the skills to expertly navigate the intricate regulatory environments, ensuring strict compliance with Audit, Financial Crimes, Fraud, KYC, Cybersecurity, and Data protection standards. I am proficient in leveraging emerging technologies to bolster operational efficiency and security, making me an expert in compliance, internal audits, and risk management. In my role as Head of Compliance, I spearhead regulatory strategies, conduct thorough risk assessments, and drive automation initiatives within the fast-paced realm of digital banking. My commitment to integrity, adaptability to ever-changing regulations, and dedication to cultivating a transparent culture are instrumental in propelling our fintech's growth and solidifying our status as a reliable financial ally.

Regulatory Compliance
Compliance Testing
Compliance Consultation
Training
Risk Management
Internal Control
Internal Auditing
AI Compliance
Fraud Detection
Financial Audit
FinTech Consulting
Investigative Reporting
GDPR Compliance Review
Government Reporting Compliance
Policy Development
$15 hourly
M. Ammar A.
- 5.0/5
- (39 jobs)
✅ 13+ years of Experience ✅ ISO Consultant (9001:2015/27001:2022/BRC/UL-94-181/Food/HACCP/CCP/PRP's) ✅ Proven Results in ISO 9001, 27001, 14001, 22000, FSSC, SQF, 14064, 14065, 13485 ✅ Certified Quality Professional ✅ ISO 14064-14065 Green Gas Emission (Certification & Accreditation) ✅ ISO 14064-1,14064-2,14064-3 (Verification and Validation) ✅ SAP S4/HANA QM Certified ✅ SQFI Implementation Expert ✅ Internal Audit Expert ✅ Policy Writing ✅ SOP Specialist ✅ Company Policies and Procedures Manual ✅ Work Instruction & Checklist Draft Specialist ✅ FDA Regulations (Food, BRC, REACH) ✅ Data Visualization Expert ✅ Process Optimization Pro ✅ Process Mapping ✅ Document Control ✅ Manufacturing Data Specialist ✅ Virtual Assistance ✅ Business Process Design ⚡ Comprehensive Auditing: In-depth audits for ISO 9001 (Quality Management Systems) and ISO 27001 (Information Security Management Systems), ensuring compliance and identifying areas for improvement. ⚡ Customized Solutions: Tailored advice and strategies to meet your specific organizational needs, while aligning with international standards. ⚡ Continuous Improvement: Guidance on implementing best practices for ongoing quality and security enhancements. ⚡ Risk Management: Expert analysis and recommendations to mitigate risks, ensuring robust and resilient systems. ⚡ Training and Support: Providing staff training and support to understand and effectively implement ISO standards. 🚀Specialized Expertise🚀 in Quality Control, Assurance, and Audit Management across diverse sectors including manufacturing, healthcare, food, petrochemical, and automotive industries, I have consistently demonstrated leadership in achieving ISO 9001, BRC, ISO 27001, and ISO 14001 certifications. My proficiency extends to Data Visualization, where I leverage advanced techniques to drive insights and informed decision-making. In addition to my certification leadership, I have successfully spearheaded process safety initiatives and optimized business processes. My adeptness in SAP implementation and Quality Management (QM) ensures seamless operations and adherence to best practices. Furthermore, I possess a strong track record in complaint handling and process optimization. As an ISO Consultant and Writer, I am dedicated to crafting meticulous Policy & Procedure Documentation aligned with ISO standards, while ensuring full compliance with GDPR requirements. My commitment to excellence is evident in my punctual delivery and relentless pursuit of customer satisfaction, reinforced by consistently positive client feedback. In all my endeavors, I priorities not only quality and efficiency but also the safeguarding of data protection and privacy, thereby fostering trust and confidence in every project undertaken.

Regulatory Compliance
Compliance
Food Packaging
Procedure Development
Policy Writing
Quality Audit
Master Data Management
Audition Preparation
Internal Auditing
Quality Assurance
Quality Management System
ISO 14001
ISO 27001
ISO 9001
$15 hourly
Nimra S.
- 4.7/5
- (1 job)
I have done M.Sc in Chemistry and worked in a Homoeopathic pharmaceutical company as Quality control officer and Regulatory specialist for past four years. I have experience in creating product dossiers, verifying and developing content for packaging and advertisement material. Services I offer: 1. Regulatory Writing: I specialize in preparing accurate and compliant product dossiers for registration, ensuring all necessary documentation is organized and submitted. 2. Homoeopathic Formulations: I can help in development of homoeopathic formulations as per regulatory compliance. 3. Research: I can provide data of different herbs through effective research. 4. Packaging Verification : I verify packaging material descriptions including cartons, inserts, and labels, to ensure compliance with regulatory standards. 5. Content Development: I can help to develop content for inserts, cartons, labels of new products, advertising material and content for websites which is effectively communicating product information and benefits to consumers. 6. Regulatory Compliance Consulting: With in-depth knowledge of homoeopathic pharmaceuticals, I offer consultancy services, guiding clients through the complexities of regulatory requirements, documentation, and labeling.

Regulatory Compliance
Content Development
Product Formulation
Research & Development
$20 hourly
Maria K.
- 4.9/5
- (2 jobs)
Hi, I'm Maria K 👋 I'm a Writer, Business Development, and Marketing Expert, and I help businesses like yours grow through impactful strategies, compelling content, and smart marketing execution. With over 6 years of experience, I specialize in turning your ideas into actionable plans that deliver results. → My work has helped businesses scale, reach new audiences, and increase conversions → I’ve crafted persuasive copy for websites, landing pages, email campaigns, and business proposals for top-tier clients → I've helped startups and established businesses create and execute marketing strategies that lead to sustained growth What I do best: →Business Development: I work with you to design and implement business strategies that fuel your growth, boost your presence in the market, and increase profitability. Whether you're just starting out or looking to scale, I have a proven track record of success. →Marketing Plans & Execution: From in-depth market research to competitive analysis, I build marketing plans that align with your business goals and help you execute them flawlessly. I specialize in data-driven strategies, making sure that every decision is backed by insights. →Copywriting: Whether it’s for email campaigns, websites, landing pages, business proposals, or video scripts, I write persuasive, engaging copy that grabs attention and converts visitors into loyal customers. I know exactly how to make words work for you. →Social Media Management: With strategic social media management, I’ll elevate your brand’s online presence, create engaging content, and grow your community. From Instagram to LinkedIn, I manage it all to help you connect with your audience. →Additional Services: I’m not just a one-trick pony. From creating business plans and strategies to executing them and everything in between, I’m ready to take on projects that drive real results. →Social Media Post Design & Content services Let’s work together to take your business to new heights! I’m here to help you build your brand, execute marketing strategies, and deliver copy that converts. Feel free to reach out—I’m always available to discuss your next big project or idea. Let’s create something amazing! The Longer, Sit-Down Version: It’s a pleasure to meet you! I’m Maria K, and I bring a combination of creativity, business insight, and marketing expertise to the table. Throughout my career, I’ve had the privilege of helping businesses grow by crafting strong strategies, delivering top-notch copywriting, and executing marketing plans that get results. My approach is to understand your business inside and out, so I can develop tailored strategies that make a real difference. Whether you’re a startup looking to make your mark or an established business ready to expand, I specialize in the following: →Business Development: Creating and executing business strategies that fuel growth, optimize processes, and increase your market share. →Marketing Plans & Execution: Data-driven plans and campaigns that align with your goals. I ensure every marketing move is backed by research, insight, and industry best practices. →Copywriting: Writing that speaks directly to your audience. Whether it’s for a website, email campaign, landing page, or business proposal, I know how to craft persuasive, action-driving copy. →Social Media Management: Strategically growing your online presence through engaging content that builds your brand and connects with your audience. →Strategic Execution: I don’t just create plans—I help you put them into action with precision, ensuring results at every step. I’m passionate about what I do, and I take pride in delivering quality work that exceeds your expectations. Every project I take on is an opportunity to contribute to your success. If you're ready to elevate your business and execute marketing strategies that drive real results, let’s chat! I’m excited to help you bring your vision to life. Cheers, Maria K P.S. – If you’re working on something unique or have specific challenges, don’t hesitate to reach out! I love tackling new projects and coming up with creative solutions.

Regulatory Compliance
Research & Development
Technical Writing
Government Reporting Compliance
Compliance
Policy Writing
Policy Analysis
Document Analysis
Compliance Training
Business Writing
Compliance Consultation
Training Materials
User Manual
Procedure Manual
Company Policy
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