Assist with the case processing, submission, tracking and maintenance of individual case safety report and medical device report documents involving approved products.
Assist with the processing, submission, tracking and maintenance of safety report...
- Drafting various deeds and Documents and Contracts etc.
- Tender documents, Development Agreement,Lease Deed,Leave and License Agreement
- Handling Property, intellectual property rights, Registrations,Customer Queries
• New Business development for Finished Formulations.
• Market research & competitor analysis for business development.
• Marketing of existing products and services & evaluating market potential for new products.
• To look after the regis...
Key Skills : sales executive,marketing executive,business development executive,bpo executive
Searching in different patent databases and analyzing patent publications.
• Perform various other types of patent analyses, such as, claims mapping, portfolio analysis, patent
categorization, patent valuation etc.
• (Assessment) in el...
Key Skills : candidate should be having post graduate diploma in patent law/ ipr.,candidate should be focussed,a good learner,and good written,candidate should...
Candidate with 3-5 year of experience in regulatory filing for ROW and Semi- regulated marked for Injectable Formulation.
Advantage if handled eCTD submission and exposure of Regulated Market and other Dosage form.
Should be capable of handling...
Archivist Core responsibilities include
Conduct data archival awareness and training sessions
Has good understanding of Data retention requirement on business needs and financial, legal and regulatory requirements
Coordination with Business Stake...
Key Skills : records management data management cost saving archival ass,records management,data management,archivist,legal advisor,consultant,legal...
Coordination with departments for dossier planning, preparation & approval as per Country Guidelines, Query Handling, Art Work Review, Registration process of products in new countries, Impartation of trainings ICH, CTD & ACTD Guidelines etc.
Key Skills : ctd,actd,ich,dossier,art work review,registration of products,pharmacist,pharmacy manager,pharmacy incharge,pharma associate
Review, draft, and implement legal regulatory and compliance programs; provide necessary training relative to rollout of new initiatives
Select, test, and implement software programs to facilitate compliance requirements including procedure drafting...
Review of Legal Contracts and Documents Viz. : Sale and Service Agreements, Partnership Agreements, Lease and License Agreements, Employment Contracts, Due Diligence, Non Disclosure Agreements, Etc.
- Regular Correspondence with the Parent Company a...
Given in an opportunity to work closely within a Pharmaceutical & Biotechnology consulting company, you will be able to catalyze the organizational growth by providing regulatory in-sights for specific products for Indian market.
5 to 20 years experience in Legal/ Liaisoning
- Should have hands on experience in coordinating with all govt.
- Legal / Govt. letter drafting skill is must.
- Typing knowledge (Hindi & English)
- Ensuring statutory c...
Description: Enroll For Full Time/Part Time Clinical Research Course In ProRelix & Grab Your Chance to Work In Pharma/CROs/SMOs/IT/Hospitals.
Exp: 0-3 year
Annual Salary: 1.2-2.4 lakh/annum
Courses Full Time & Part Time: Clinical Research Sy...
Key Skills : clinical research executive,research associate
- Preparation and compilation of Module 2, 3, 4 and 5 for the regulated markets (Europe/Australia/Canada) in CTD/eCTD format.
- Handling queries on Quality, Clinical, Non-clinical and Bio-equivalence parts received from the different regulatory auth...
Central Drugs Standard Control Organisation (CDSCO) FDA Bhawan, New Delhi
RS Up To 3,25,000 Hyderabad, Sector 18 Chandigarh, South Delhi, East Delhi, Central Delhi, Mohali, Roorkee, Delhi
Import & Registration Division:
•Scrutinize & examine the Drug Master Files (DMF), Plant Master File (PMF), GMP certificates & COPP etc. from overseas manufacturing units pertaining to Registration & Import License of Drugs, under Form 41, a...
Key Skills : drug regulatory affair,clinical research,epidemilogist,pharmacovigilance,technical documents
Hiring Life Science Graduates with experience and TRAINED in CRA/CRO/CDM/PV/Regulatory
• Any Life Science graduate with an exposure to Clinical research domain
• Having a prior exposure/experience in Clinical document management/ Clinical d...
Key Skills : clinical data coordinator,clinical research associate,clinical research analyst,clinical data management,pharmacovigilance,medical coding,regulatory,...
1. post Offered: Law Officer in a Limited Company
o candidates Should have Bachelor's Degree in Law (llb or Equivalent – Full Time Degree) from Recognized Indian Universities. the Degree Should also Enjoy Recogni...
We are looking for Customer Sales Representative for our client in pharmaceutical industry to sell their online pharma courses and trainings.
The candidate should have experience of handling and making (inbound/outbound) calls to prospective custome...
Post Offered: Law Officer
Location: Samrala, Distt. Ludhiana,Punjab
o Candidates should have Bachelor\'s degree in Law (LLB or equivalent – full time degree) from recognized Indian Universities. The degree should also enjoy...
Key Skills : law officer,legal services,legal consultant,legal advisor
Drafting various contracts as per the requirement of each respective business vertical.
Reviewing and providing comments and suggesting changes in order to protect the interest of the company on contracts forwarded for inputs.
- Reviewing Doc From Adl, R&D, Quality & Prod.
- Life Cycle Management Through Amendments / Annual Reports.
- Managing Databases And Up-Keeping Of Recording Systems
- Preparation And Reviewing Of Regulatory Dmf.
- Response To Customer Dmf...
Should able to handle all company legal matter\'s.
2. Should consult and assist in legal matter\'s.
3. Liable for drafting the legal documentations as per Company requirements.
Salary: 1,00,000 - 1,25,000 P.A
Industry:Construction / Engineering /...
Strong With Regulatory Documentation
Mfr/Sop/Amv(Analytical Method Varidation),Actd/Ctd, Dossier Preparation
Having A Sound Knowledge Of Bmr Preparation And Filing, Fr&D Documentation, Pv Etc
Will Be Responsible For Handling Regulatory Affai...
Advocates Who Can Independently Handle Litigation and Has Excellent Drafting Skills.
salary: Commensurate with Experience.
functional Area: Legal , Regulatory , Intellectual Property
role: Law Officer
Work Under Fair Knowledge of Company Law & all Work Related with Registrar of Companies
drafting & Vetting of Various Agreements such as Leave & License Agreements, Non-disclosure Agreements, Distributorship Agreements Etc. Internet & Roc Searche...
1. Take Care of Legal Issues with the Company.
2. to Draft Documents, Review It.
3. Responsible for Documentation, Maintaining Legal Files.
salary: 1,00,000 - 2,00,000 P.a
industry: Real Estate / Property
functional Area: Legal, Regulator...