Average salary: Rs270,000 /yearly

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Search Results: 5,666 vacancies

 ...Schedule Full-Time Located Remotely? N Relocation? N Position Type Management JOB SUMMARY Manages all maintenance operations,...  ...maintenance and energy conservation. Responsible for maintaining regulatory requirements. Leads the emergency response team for all facility... 
Bodakdev
3 days ago

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... 

Actide International

Vadodara
16 days ago

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... 

Actide International

Vadodara
16 days ago

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.... 

Renown Pharmaceuticals Pvt. Ltd.

Vadodara
3 days ago

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... 

Actide International

Vadodara
16 days ago

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... 

SDP HR Solution

Vadodara
more than 2 months ago
 ...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.... 

United HR Solution

Ahmedabad
28 days ago

Rs 10 - 20 lakhs p.a.

 ...We are looking for an experienced Project Manager to manage organization of key client projects.   Responsibilities Coordinate internal...  ...performance using appropriate systems, tools, and techniques. Report and escalate to management as needed. Manage the relationship... 

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Gandhinagar
16 days ago

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... 

Actide International

Vadodara
16 days ago

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-... 

AG Digital Marketing

Ahmedabad
1 day ago

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)... 

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Gandhinagar
a month ago
 ...institutional investors like Augment Infrastructure a USbased fund manager Danish Investment Fund (IFU) and UK Climate Investments (UKCI) a...  ...with the F&A team for prompt receipt of energy adjustment reports and timely invoice generation. Ensure prompt receipt of surplus... 

Saaki Argus & Averil Consulting

Vadodara
more than 2 months ago

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... 

Actide International

Vadodara
16 days ago

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... 

Actide International

Vadodara
16 days ago

Rs 2 - 5 lakhs p.a.

 ...001:2015, EN ISO 13485: 2016, Quality management System, WHO-GMP, EU MDR 2017/745, IMDR...  ...File for CE Submission accordance with regulatory guidelines. ? Exposure of various...  ...instruments. ? Preparing Annual product review report. ? Prepare checklist for the warehouse... 

Actide International

Surat
16 days ago

Rs 25 - 30 lakhs p.a.

 ...Position: Factory Manager Location: Sarigam near by Vapi  Experience: 15- 20 Years Industries: Chemical Age: Upto 45 Years...  ...identify and resolve any production issues. Preparing production reports and submitting them to key decision-makers. Regularly... 

Quality HR Services

Vapi
16 days ago

Rs 10 - 15 lakhs p.a.

 ...Sr. No Details 1 The EHS Manager is Responsible for smooth running of Effluent treatment plant (ETP), Reverse Osmosis (RO), Multiple...  .../expected results 10 Preparation of Monthly and Annual reports (CCE EC CTE compliance) 11 Capable to run the plant with Zero... 

SDP HR Solution

Bharuch
16 days ago
 ...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... 

PDA Consultants

Rajkot
more than 2 months ago
#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...

Swiss Parenterals Ltd

Ahmedabad
3 days ago

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... 

Actide International

Vadodara
16 days ago