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Executive Regulatory Affairs -- 2

₹100-400 INR / hour

Closed
Posted over 3 years ago

₹100-400 INR / hour

Roles and Responsibilities Coordination with in-house R&D / Mfg units for obtaining various regulatory data for preparing dossier. Preparation of scientific reports based on analysis, MSDS, HPCL/ GC and other tests at lab & field level. Verify Specification, Certificate of Analysis & Method of Analysis of Active, Finished Product. Arrange Technical Documents & Samples for Registration as per Country Specific Regulatory [login to view URL] of Good Quality Registration Dossiers with some timelines. Product Patent analysis Compilation of Data Sheet for Formulation/Technical Products Preparation of MSDS/Technical Data Sheet for Products Any other responsibility assigned by management on the basis of requirement
Project ID: 27248780

About the project

8 proposals
Remote project
Active 3 yrs ago

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8 freelancers are bidding on average ₹839 INR/hour for this job
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Hi there, I have read your project entitled “Executive Regulatory Affairs” I am a Certified Chartered Accountant and a duly certified mentor of ACCA (UK). I have already done numerous projects of this sort. You can see my portfolio for this purpose https://www.freelancer.com/u/SIBTEHASSANBUTT I will deliver you the whole project whenever you need it. I will be happy to provide you with any revisions if you needed any. Let me do this job for you in a professional manner. After assigning me this project you need not worry about anything. looking forward to working with you. Experienced and competent finance professional with 5 years of experience, Knowledge and application of International Financial Reporting Standards (IFRS) and International Standards on Auditing, Knowledge of Corporate laws and Procurement Rules, Sound analytical and problem-solving skills, internal controls, Budgeting, Financial Reporting, Financial Modelling, Accounting Software, ERP, MS Excel, MS Word. My specialities are: -Payable & Receivables -Financial Data Entry -Finance, Management Accounting, Auditing & Bookkeeping, Accounting, -Financial Statements. -MIS, Budgeting, Forecasting & Variance Analysis. -Payroll -Audit of books of accounts. -Taxes -Reconciliations including banks, vendor, suppliers, financials. -Fixed Assets accounting & preparation of the register, calculation of depreciation aa Thanks. Member ACCA (UK), ACA (UK) finalist
₹5,000 INR in 40 days
5.0 (6 reviews)
2.8
2.8
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FREELANCER Hello I am Rajesh Singh I am Rajesh Singh , I am Well specified content writer If you need a well content writer to do your project , In that case I am best . What are the things you need in a content writer Adapatabillity , Strong Research skills , A Solid Understanding of SEO , Oraganisiation Skills The ability to get focused , The ability to meet deadlines , Communicate , Editing editing and more editing I have all the requisite qualities that are required for content writer.
₹250 INR in 40 days
0.0 (0 reviews)
0.0
0.0
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I want to work with u. My typing speed is 50 word per min. I am also know Microsoft word, excel very well. I am also good at online browsing. SO please give me a chance. I am trying my best.
₹250 INR in 4 days
0.0 (1 review)
0.0
0.0
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Hi, I have gone through your Job Description which suiting me I can fulfill your tasks on time. as I have an Experience in Regulatory affairs filings Dossier Submission for Asean,Africa, GCC, & Country Requirement dossiers, CTD, ACTD, I have required experience into the Regulatory affairs and I can Co-ordinate with the cross-functional teams QA, QC,R&D, Production for Documents to Compile in Dossier, BMR, BPR, MFR, COAS, Validation reports, Stability Reports, Packing requirements, Labelling and any other requirements.
₹333 INR in 18 days
0.0 (0 reviews)
0.0
0.0
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Hello, I understand your requirement and having a rich experience of 7 years in the field of dug regulatory affairs for all dosage form. I can compile ctd, actd dossier in 1 day only if the doocuments are availble. If documents are not availble then the task may take 3 to 4 days.. Coordination with the different departments for collecting the data, review and compilation was included in my job profile.. The work will be done with higher accuracy considering the current guidlines and updated versions of pharmacopoeia.
₹278 INR in 30 days
0.0 (0 reviews)
0.0
0.0
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I have very well knowledge and experience on non-clinical as well as clinical studies. I also have knowledge on ich guidelines gcp, glp, and gmp. I am well aware of regulatory submissions and dossier preparations. I can accomplish the work within stipulated time without any errors.
₹200 INR in 40 days
0.0 (0 reviews)
0.0
0.0

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Flag of INDIA
Faridabad, India
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Member since Sep 3, 2020

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