Average salary: Rs558,571 /yearly
More statsSearch Results: 4,906 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...
...documentation as appropriate also to escalate
internally and report to manager.
3. Prepare and submit registration dossiers as per CTD/... ...5. Dispatch of registration dossiers to the National Drug
Regulatory Authorities (NDRA)/agents as applicable.
6. Actively finding...
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...
...having repacking unit in Gandhidham and Corporate office in Ahmedabad
Position : Regulatory Affairs Officer
Job Location : Bodakdev (Ahmedabad)
Reports To ; Regulatory Manager
Job Profile:
The position would be responsible for :
1. Request, follow-...
Rs 10 - 15 lakhs p.a.
...Description
-Compilation and submission of eCTD dossier for new product application (ANDA/EU-MA)/Post approval submission to the regulatory authority (specifically EU/US)
-Hand on experience in preparation of CTD section as per regulatory requirements of different region...
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...
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...
Rs 6 - 7 lakhs p.a.
...Job Description: Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for... ...time-frames.
? Responsible for planning, coordinating and managing day to day regulatory affairs activities in a timely manner....
Rs 2 - 5 lakhs p.a.
...required for the ISO 9001:2015,
EN ISO 13485: 2016, Quality management System, WHO-GMP, EU MDR 2017/745,
IMDR 2017.
? Knowledge and... ...(TMF) and Design File for CE
Submission accordance with regulatory guidelines.
? Exposure of various countries regulatory such as...
...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...
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...
...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...
...protocols.
- Write, and edit clinical study protocols. clinical study reports, summary documents, investigator brochures, portions of regulatory briefing documents, and development safety update reports.
- Drafting and revising pre-clinical summaries.
- Quality control...
...Core Responsibilities
Relationship Management :
Managing the banking and investments relationship of YES FIRST clients and responsible... ...risk policy and processes to mitigate the operational, regulatory, financial, informational, reputational and audit risks as instructed...
...Time
Located Remotely? N
Relocation? N
Position Type Management
JOB SUMMARY
Manages all maintenance operations, including... ...and energy conservation. Responsible for maintaining regulatory requirements. Leads the emergency response team for all facility...
...seeking to work with a major Indian corporation to provide Project Management Consultant (PMC) Services and Engineering Procurement and... ...'s technical submittals within schedule.
~ Writes technical, regulatory, and performance reports and provides documentation to senior management...
...Job Title: Sales Manager
Company: Aditya Birla Housing Capital
Location: [Specify location]
Job Type: Full-time
Job Summary... ...promotions.
# Ensure compliance with company policies, procedures, and regulatory requirements.
# Continuously assess and improve sales...
...Job Purpose Responsible for establishing and managing the Quality Management & Assurance systems in conformance with regulatory requirements (DGCA) for NSOP and governance standards. Ensuring that all quality related policies, manuals and procedures for the company are aligned...
