RA Executive Jobs

Job Description Billing & Planning EngineerQuantet Builders Pvt. Ltd. a growing and quality-driven construction company, is looking for a skilled Billing & Planning Engineer to join our project team.The ideal candidate must have strong expertise in RA billing, BOQ management, quantity take-offs, project scheduling, and progress monitoring.We value professionals who are accurate, responsible, and committed to timely project delivery.Experience: 1 - 6 yearsQualification: Diploma/B.Tech (Civil)Skills Required: Billing, Planning, Excel, AutoCAD, Measurement Sheets, CoordinationLocation: LudhianaSalary: Best as per industry standards

Responsible for ensuring that all regulatory requirements for the manufacture, testing, and approval of injectable pharmaceutical products are met. This includes preparing and submitting regulatory filings to the relevant authorities, maintaining compliance with applicable laws and guidelines, and ensuring that the injectable products are developed and marketed in accordance with regulatory standards.

Hiring for 30 Airport Executive Jobs in Kolkata,Patna,Howrah,Darjeeling,Asansol,Jamshedpur,Hooghly,Bhubaneswar, for Freshers,Required Educational Qualification is : Higher Secondary, Secondary School, Other Bachelor Degree with Good knowledge in Aviation,Airport Ground Staff,Airport Cargo Loader,Ground Handling etc.

Designation: Sr. Officer / Executive/ Sr. Executive (Regulatory Affairs USA, EU, JAPAN,ANVISA, TGA market)Experience:- 3 to 6 years' work experience in international and domestic Pharma regulatory affairs.- Confirmed knowledge of Global market regulatory requirements and ICH guidelines.- Should have experience in eCTD DMF/Dossier preparation and review including life cyclemanagement, specifically CMC writing & preparing module 1, 2 and 3 previously.- Should have experience in handling of changes notification to customers and agencies- Should have experience in renewal of facility registrations and drug listing activities.- He/she has to work independently. There is no scope for supervision or team handling.- Only M.Sc Chemistry preferably or complete experience in API industry for BPharm /MPharm .Job Responsibilities:- Preparing DMF/dossiers for regulated and semi-regulated markets.- Preparation of documents for domestic license permissions.- Gathering, evaluating, organizing and managing drug substances and intermediatesregulatory information in a variety of formats.- Handling of change notifications with the customers and regulatory agencies- Maintaining Regulatory database up to date.- Address customer complaints and queries within agreed timelines.- Attending various customer and health authority audits held at the manufacturing site- Keeping up-to-date with changes in regulatory legislation and guidelines- Writing comprehensible, user-friendly, clear process description and impurity profile- Ensuring that high quality standards are met and submissions meet strict deadlines.Primary Skills:Understanding on API process and analytical methods development flowKnowledge on impurity profile, analytical method validations and stability studies.Knowledge on eCTD submission structure.Fluency in oral and written English.Able to build and maintain good communication with cross functional departments

Hi,we have an urgent vacancy in Regulatory Affairs for a pharmaceuticals company.experience - 2-12 yearsLocation - Ahemdabadinterested candidates, please share your resume or references on