Average salary: Rs270,000 /yearly
More statsSearch Results: 5,603 vacancies
...Join our team at Scipex Consultants, a dynamic and rapidly growing consulting firm, as a Manager - Regulatory Toxicology. This role requires a high level of expertise in toxicology , particularly for cosmetics, consumer products, and OTC products along with a dedication to...
Rs 2.4 - 3 lakhs p.a.
...format in countries of African Region, Cambodia, Myanmar, CIS
To manage new registration / preregistration / query response / variation... ...(preferred in Working with merchant exporter)
Dossier,Regulatory Affair,Drug Regulatory Affair,COPP
Designation: Regulatory...
Rs 3 lakh p.a.
...products specification, manufacturing process,
Product development report, stability reports, process validations preparation & review.... ...Master File review
- Technical query response to the various regulatory authorities.
Ideal Profile
~ You have at least 1 year post-...
Rs 5 - 6 lakhs p.a.
...They must have excellent organizational, analytical, project management, and communication skills.
They work frequently with other employees... ...complex activities, often with competing priorities.
Most regulatory affairs positions are full time.
Regulatory...
...manufacturer where applicable.
2. Assess and report deficiencies to the manufacturer and... ...to escalate
internally and report to manager.
3. Prepare and submit registration dossiers... ...dossiers to the National Drug
Regulatory Authorities (NDRA)/agents as applicable....
Rs 10 - 15 lakhs p.a.
...product application (ANDA/EU-MA)/Post approval submission to the regulatory authority (specifically EU/US)
-Hand on experience in... ...experience in preparation of query response and PAS, CBE and annual report.
-Have ability to co-ordinate with cross functional team
-Having...
Rs 3 - 4 lakhs p.a.
...Responsibilities :
Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to... ...information to Production, QA, QC and R&D departments and senior management as required.
Salary shall be commensurate to experience and...
#ROW MARKET #CIS #MENA #AFRICA #LATIN #ASIA #EUROPE MARKET
Vacancy - 15
Qualification - B.Pharm/M.Pharm
Job Description :
Sound knowledge of CTD/ECTD/ACTD dossier review of OSD/Parenteral dosage forms.
Excellent knowledge of ICH/Country specific/Variation...
...Prepare routine reports by gathering data from the various systems within Company that result in meaningful
and actionable insight... ...charts and/or graphs.
Provide regular reports and updates for management and leadership.
Prepare key insights based on data analysis...
Rs 4.8 - 5 lakhs p.a.
...in Ahmedabad
Qualifications and Skills:
Experience in regulatory affairs within the pharmaceutical sector
Knowledge of... ...functional teams to ensure regulatory compliance
Handle regulatory reporting and maintain accurate records
Contact Person:
Srushti...
Rs 6 - 7 lakhs p.a.
...Job Description: Experience in handling regulatory affairs for ROW market mainly Central and... ...by QA, QC, Production providing them the report of shortcomings & ensures them to correct... ...Responsible for planning, coordinating and managing day to day regulatory affairs activities...
Rs 18000 - Rs 25000 per month
...highest quality standards and aims to be a top producer of soft gelatin capsules in India. Renown Pharma is known for its adherence to regulatory standards like MHRA, TGA, and WHO-GMP, providing contract manufacturing services for nutraceutical and therapeutic formulations....
Rs 2 - 3 lakhs p.a.
...• Monitor the Ready for Review Queue daily
• Review submitted reports by following designated checklists or technology to ensure the report... ...is a requirement
• Perform other duties as assigned by management QC REVISIONS
Purpose-
The Quality Control Revisions Specialist...
Rs 3 - 4.2 lakhs p.a.
...ISO 9001:2015, EN ISO 13485: 2016, Quality management System, WHO-GMP, EU MDR 2017/745, IMDR 20... ...File for CE Submission accordance with regulatory guidelines.
Exposure of various countries... ....
Preparing Annual product review report.
Prepare checklist for the warehouse and...
Rs 3 - 5 lakhs p.a.
...plan and develop product trials and interpret trial data
advise scientists and manufacturers on regulatory requirements
provide strategic advice to senior management throughout the development of a new product
project manage teams of colleagues involved with the development...
...DeveloperJob description:As a BI Developer, you will develop Power BI reports and interactive dashboards for various internal departments.... ...trends in BI and data visualization.- As an analyst in the data management Team, you will be a key member of our Data Analytics Pillar.- To...
Rs 2 - 5 lakhs p.a.
...~ Preparation and review the dossier of as per current prescribed guidelines of the respective regulatory authority.
~ Well versed with the guidelines of ICH and other regulatory.
~ Preparation of documents for license application.
~ Preparation of documents for...
...Dear Candidate,
Greetings from Pegasus Corporate!!
Location: Ahmedabad
Opening: Manager / Sr. Manager International Regulatory Affairs
Duties
1. Market : ROW, US & Europe Market
2. Exposure : Hands on experience in :
- New US ANDA dossier Preparation, compilation...
...This role will support South America and Europe :
- Develop new regulatory policies, processes and SOPs .
- Evaluate regulatory risks of... ...of initial product concepts and provide input to senior management.
- Assess the acceptability of quality, preclinical and clinical...
Rs 9 - 18 lakhs p.a.
...ERD,) and end - user resources.
Working as a part of a team to manage and deliver quality and robust system enhancements to critical... ...Factory,CSV files,Data Warehouse
Designation: ETL Developer + Report Writer
Vacancies: 2
Experience: 5.0 Year(s) - 8.0 Year(s)...
