Regulatory Affairs Manager - Navi Mumbai

The Manager Regulatory Affairs will prepare and review CTD and ACTD dossier. · ...

+Job summary · The role contributes to the institute's mission by navigating complex legal landscapes and protecting its interests. · +QualificationsGraduation in Law from a premium institute. · ...

The candidate will be responsible for managing regulatory affairs for pharmaceutical formulations. · ...

Ensure obtaining of necessary Projects & manufacturing units related statutory approvals in a timely manner and ensuring efficient functioning of corporate affairs Department for setting up of green field manufacturing facilities with complete customer satisfaction. · Liaising wi ...

+Around 7 -8 years of experience in ROW markets. · + · Maintain up-to-date knowledge of regulatory guidelines and changes in Latam region. · Work closely with R&D departments to ensure timely submissions of dossiers, samples and other full kit requirements of customers. · ...

We are looking to hire an aggressive/dynamic Regulatory Affairs Professional for our further expansion and growth plans. This position is based at our R&D center at Turbhe Navi Mumbai and will report to the AGM - Regulatory Affairs. · Responsible for filings of MA applications fo ...

UMEDICA is a vertically integrated company engaged in manufacturing finished formulations at its facility located in Vapi (Gujarat). We are looking to hire a Manager / Sr. Manager Regulatory Affairs for our R&D center at Turbhe Navi Mumbai. · ...

+Supports the Medical Affairs function and project teams within area of expertise. · + · +Defines and delivers training for junior members of the team. · Contributes to establishing and implementing policies, procedures and standards for own work and work of others, ensuring comp ...

Serve as a country or regional expert supporting the Medical Affairs function and project teams within a defined area of expertise Act as a senior technical authority and primary knowledge source within the therapeutic or functional specialty. · ...

The role involves hands-on responsibility for compilation and filing of regulatory dossiers in regulated markets with strong exposure to EU regulatory procedures. · Should have hands on experience about dossier filing compilation in regulated market. · Knowledge about EU procedur ...

Manager Regulatory Affairs (EU/UK): Handle EU & UK MA filings, eCTD submissions, lifecycle management & variations. · 14+ yrs pharma regulatory exp. · ...

To manage and execute regulatory strategies, submissions, approvals, · and lifecycle management activities for pharmaceutical products across ROW markets. · ...

With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the leading company solely dedicated to skin and advancing the future of dermatology. · We look for people who focus on getting results, embrace learning and bring a positive energy. Th ...

Role Brief: · Responsible for survey, Rehabilitation of a cluster of slum dwellers through the process of tenant management. Responsible for managing the end to end process of tenant management for a cluster / project. · Roles and Responsibilities · Policy · Possess a thorough un ...

The role will involve expertise in D & C Act and Rules as well as FSSAI regulations with experience in FDA related activities. This profile will ensure timely and robust functional/cross-functional coordination (R&D, QC, Marketing, Legal, Production etc.) transparent execution an ...

Handle regulatory affairs activities related to APIs and pharmaceutical intermediates)prepare submissions and updates. · ...

NuVvaGen Bioscience is an export-focused manufacturing company renowned for its advanced automation and state-of-the-art infrastructure. The facility spans 100,000 square feet and is equipped with PLC/VFD-enabled machinery to ensure high production efficiency. · Preparation and f ...

We look for people who focus on getting results, embrace learning and bring a positive energy. · ...

We look for people who focus on getting results, embrace learning and bring a positive energy. · ...

The Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. · Bachelor degree in Biological Sciences eg BioMedical, Biochemistry, Pharmac ...