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2.0 - 6.0 years
0 Lacs
gujarat
On-site
You will be responsible for coordinating with the plant and preparing online offline applications through portals like Sugam, ONDLS, NSWS, and NDPS. Key Responsibilities: - Coordinate with the plant for commercial activities - Prepare online offline applications through portals such as Sugam, ONDLS, NSWS, and NDPS Qualifications Required: - Previous experience working as an Assistant Manager or similar role - Strong management skills Please note that there are no additional details about the company provided in the job description.,
Posted 3 weeks ago
10.0 - 15.0 years
15 - 18 Lacs
ludhiana
Work from Office
Position: Senior Manager Quality Assurance Experience: Minimum 10-15 years Notice: 30 days (maximum) Company: Leeford Healthcare Limited www.leeford.in https://www.linkedin.com/company/1464125/admin/dashboard/ Location: Ludhiana Education: B.Pharma/M.Pharma or B.Sc/M.Sc Skills Required Excellent data analysing and review skills, Strong technical and audit skills, Great eye for detail, Ability to teach and mentor, Flexible with the ability to and work under pressure, Proactive, strong-minded, quick thinker and assertive. Work Profile: Creates and implements company quality standards at Loan License sites. Should have extensive knowledge of working on online portals like NPPA / Sugam / ONDLS. ...
Posted 1 month ago
8.0 - 12.0 years
0 Lacs
mumbai, maharashtra, india
On-site
Primary Job Function To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations. The role is critical to maintaining business continuity and regulatory compliance. Core Job Responsibilities Regulatory Submissions and compliance Prepare and submit various applications such as additional product permission, Layout approval, facility modification approval, technical person approval, Test license, amendments in licenses, State GMP and GLP certificate applications, post approval changes e...
Posted 2 months ago
8.0 - 12.0 years
0 Lacs
mumbai, maharashtra, india
On-site
Primary Job Function To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations. The role is critical to maintaining business continuity and regulatory compliance. Core Job Responsibilities Regulatory Submissions and compliance Prepare and submit various applications such as additional product permission, Layout approval, facility modification approval, technical person approval, Test license, amendments in licenses, State GMP and GLP certificate applications, post approval changes e...
Posted 3 months ago
2.0 - 6.0 years
0 Lacs
gujarat
On-site
You will be responsible for coordinating with the plant and preparing online/offline applications through portals like Sugam, ONDLS, NSWS, and NDPS. Key Responsibilities: - Coordinate with the plant for commercial activities - Prepare online and offline applications through portals such as Sugam, ONDLS, NSWS, and NDPS Qualifications Required: - Previous experience as an Assistant Manager or in a similar managerial role - Strong management skills Please note that this job is based in the Corporate Office in Gujarat, IN and is offered by Dishman Carbogen Amcis Limited.,
Posted 3 months ago
8.0 - 12.0 years
0 Lacs
mumbai, maharashtra, india
On-site
JOB DESCRIPTION: Primary Job Function: To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations. The role is critical to maintaining business continuity and regulatory compliance. Core Job Responsibilities: Regulatory Submissions and compliance Prepare and submit various applications such as additional product permission, Layout approval, facility modification approval, technical person approval, Test license, amendments in licenses, State GMP and GLP certificate applications, post...
Posted 4 months ago
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