Search Results: 22,217 vacancies
...About the job
Site Name: Bengaluru Luxor North Tower
Key Responsibilities :
Accountable to the GRL and Global Regulatory staff for the delivery of Marketing Application preapproval/investigational and lifecycle maintenance submissions to agreed timelines and in compliance...
...5. Dispatch of registration dossiers to the National Drug
Regulatory Authorities (NDRA)/agents as applicable.
6. Actively finding... ...on MP connect Registration and NDRA
overview.
9. Coordinate with MP agents and Country Managers on
handling regulatory...
...Department:
Regulatory Affairs CMC & Device
Are you passionate about what you are doing? Do you want to build excellence within processes... ...part of combination products. This role involves planning, coordinating and executing the regulatory tasks as required for existing...
...Department : RA Labelling
Are you passionate about ensuring regulatory compliance and driving high-quality global packaging materials... ...with stakeholders ranging from labelling development to coordination with Novo Nordisk RA affiliates worldwide.
Plan and drive regulatory...
...comprised of +60 experienced professionals associated with key regulatory processes covering CMC, Medical Device Reporting (MDR) and... ...device part of combination products. This role involves planning, coordinating and executing the regulatory tasks as required for existing...
...environment? Are you best at what you do? If so, raise your hand
as there is an exciting opportunity waiting for you as “CMC
Regulatory Professional II” with us. "Apply now" - At
Novo Nordisk, we assure you will experience the best.
About the department...
...and long-term business growth outlook.
Our expertise in regulatory affairs, coupled with in-depth market analysis, ensures the success... ...material and all required documents.
Application, review, coordination, follow-up of legal documents COPP, FSC, etc.
Maintain a...
Rs 2.4 - 3 lakhs p.a.
...Job responsivities are to assist Regulatory manager
Preparation, Compilation and review of registration dossier of tablet /capsule/... ...Preparation of product permission for both of export products.
Coordination with various department of manufacturing as per the...
...Position : Executive Department : Regulatory Affairs
Location : Kandivali - West, Mumbai
Qualification - M Sc/ B Pharm/ M... ...own EU submission and maintenance of customer MAs.
Discuss & Coordinate with R&D and Analytical development departments for finalization...
...Job Description
. Department: Regulatory Affairs Rare Blood Disorders
Are you passionate about driving regulatory strategy and... ...submission and approval of clinical trial applications, driving and coordinating preparation of meeting packages to Health Authorities,...
Rs 5 - 6 lakhs p.a.
...management, and communication skills.
They work frequently with other employees and team members to coordinate complex activities, often with competing priorities.
Most regulatory affairs positions are full time.
Regulatory Responsibility means a duty or...
...Department: Labelling Designers
Are you a regulatory professional looking for an exciting opportunity in the pharmaceutical industry... ...ranging from labelling development, and labelling coordination to all Novo Nordisk RA affiliates worldwide.
As part of our...
Rs 4.8 - 5 lakhs p.a.
...Overview:
Mid-Level: 4 to 6 years of experience, Full-Time position in Ahmedabad
Qualifications and Skills:
Experience in regulatory affairs within the pharmaceutical sector
Knowledge of regulatory frameworks and guidelines
Strong understanding of regulatory...
...Gandhidham and Corporate office in Ahmedabad
Position : Regulatory Affairs Officer
Job Location : Bodakdev (Ahmedabad)
Reports... ...Status updates on connect Registration and NDRA overview.
9. Coordinate with Company's agents and Country Managers on handling...
...currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices Domain to join our... ...Ministries of Health for the approvals of the devices.
3. Coordination with R&D, Plant Quality Assurance/Regulatory Affairs...
...Description
Looking for a candidate having experience in Regulatory affairs domain for one of the medical equipments manufacturng industry... ..., establishment licenses and associated product license
Coordinate activities to support supplier audits of SSU and corporate...
...being – a fundamental driver for many of us to show up and do our best each day.
Job Description
You will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics...
...day
Evaluate dossier suitability for specific territories.
Regulatory strategize, prepare and submit MAAs to Medis clients.
Engage... ...support to Medis clients to facilitate MA approvals.
Coordinate and contribute to responses to deficiency from health authorities...
Rs 3 lakh p.a.
...Analytical method validation review as per the ICH guideline.
- Drug Master File review
- Technical query response to the various regulatory authorities.
Ideal Profile
~ You have at least 1 year post-qualification experience in a similar role.
What's on Offer?...
...-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as “CMC Regulatory Professional II” with us. "Apply now" - At Novo Nordisk, we assure you will experience the best.
About the department
RA CMC &...
