Specialist - Regulatory Toxicology

Department : RA Labelling Are you passionate about ensuring regulatory compliance and driving high-quality global packaging materials? Do you have expertise in labelling and project management? We are looking for a Regulatory Specialist to join our team in Bangalore and be part of our global Regulatory Affairs (RA) hub. If you are ready for a...

Department: RA CMC & Device Are you passionate about your work? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as "RA Specialist" with us....

The position As a RA Specialist, the ideal candidate will be responsible to design RA Strategy from late stage development and throughout Life cycle of the device project, prepare and submit high quality files to the authorities achieving fast approvals. Act as an ambassador for assigned medical devices/device part of combination products. This role...

Department: RA CMC & DeviceAre you passionate about your work? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as "RA Specialist" with us. "Apply...

Department: RA Labelling Are you passionate about ensuring regulatory compliance and driving high-quality global packaging materials? Do you have expertise in labelling and project management? We are looking for a Regulatory Specialist to join our team in Bangalore and be part of our global Regulatory Affairs (RA) hub. If you are ready for a challenging and...

Department : RA Labelling Are you passionate about ensuring regulatory compliance and driving high-quality global packaging materials? Do you have expertise in labelling and project management? We are looking for a Regulatory Specialist to join our team in Bangalore and be part of our global Regulatory Affairs (RA) hub. If you are ready for a challenging...

The position As a Regulatory Specialist Labelling, you will have the following responsibilities: Set the regulatory strategy and plan, create, and drive projects to deliver high quality global packaging materials. Work as an integrated part of global cross-functional teams, collaborating with stakeholders ranging from labelling development to coordination...

Remote Work: Yes Overview: At Zebra, we are a community of innovators who come together to create new ways of working to make everyday life better. United by curiosity and care, we develop dynamic solutions that anticipate our customer's and partner's needs and solve their challenges. Being a part of Zebra Nation means being seen, heard, valued,...

Remote Work: Yes Overview: At Zebra, we extend the edge of possibility by shaping the future of work on the front line—reinventing how businesses run and moving society forward. We are a community of changemakers, innovators and doers who come together to deliver a performance edge to the front line of business. We develop new technologies and create...

Key Responsibilities Regulatory Specialist RIMS is responsible for delivering the following key services to GRA colleagues in support of achieving GRA business objectives: Responsibilities of this role are: Supervise, mentor and support the work of junior colleagues. Supports in resource analysis to the manager to ensure obligations can be met. ...

#LI-VK1 Be part of something altogether life-changing Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be...

#LI-VK1 Be part of something altogether life-changing Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be...

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, pre-approval/investigational and lifecycle maintenance submissions to agreed timelines and in compliance with Regulatory Authority regulations and guidelines and in line with GSK SOPs and...

About the jobSite Name: Bengaluru Luxor North TowerKey Responsibilities :Accountable to the GRL and Global Regulatory staff for the delivery of Marketing Application, pre-approval/investigational and lifecycle maintenance submissions to agreed timelines and in compliance with Regulatory Authority regulations and guidelines and in line with GSK SOPs and...

The job will involve: Conducting regulated study protocol reviews, data and report audits for Toxicology, Safety Assessment and Pharmacology studies. Conducting internal (study, process, facility based) inspections. Reviewing Standard Operating Procedures. Development and delivery of training to operational groups and QA. Provide advice and guidance on...

The job will involve:Conducting regulated study protocol reviews, data and report audits for Toxicology and supporting Dose Analysis Analytical chemistry audits Follow applicable approved policies and SOPs Navigate to the regulations and able read/understand specific regulations Perform review of protocols/amendments and report audits. Timely notify...

Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney...

Description : Primary contact with investigative sites during study maintenance and -when assigned-, sitestart-up activities, with responsibility for collection of the required investigator andregulatory essential documents to ensure EC/IRB/Third body/Regulatory Authoritysubmissions are made within the timelines agreed with project management and...

This is where you save and sustain livesAt Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.Baxter's products and therapies are found in almost...

Job Role: Study Director - ToxicologyJob title: Research ScientistJob location: BangaloreJob grade: 7-IAt Syngene, safety is a top priority both personally and professionally. Safety is as important as business performance, with a shared responsibility and accountability to follow safety guidelines, procedures, and standards.Mandatory expectations:Overall...