Site Readiness and Regulatory Specialist

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

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”...

    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...

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...

Title: Specialist - Regulatory ToxicologyLocation: Bangalore – Electronic City Description:As a specialist, you are responsible forUnderstanding the Global regulations like CLP, GHS etc. and creating compliant Safety Data Sheets by doing intensive data search and evaluating proper data.Understand SAP EHS and conduct appropriate data entry in SAP EHS...

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...

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...

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...

Join our growing team at Chetu as a Payroll/HR/Time Specialist! Chetu is excited to invite all skilled Payroll/HR/Time Specialist to become a valuable part of our expanding team. We believe your proven expertise in Payroll Specialist makes you a perfect match for this opportunity. Take a look at the job description below, and don't hesitate to apply...

Join our growing team at Chetu as a Payroll/HR/Time Specialist! Chetu is excited to invite all skilled Payroll/HR/Time Specialist to become a valuable part of our expanding team. We believe your proven expertise in Payroll Specialist makes you a perfect match for this opportunity. Take a look at the job description below, and don't hesitate to apply...

Job Title: Regulatory Affairs Manager I Career Level - D Introduction to role: Join our dynamic Biopharmaceuticals R&D team as a Regulatory Affairs Manager I. This role is a unique opportunity for a regulatory specialist with project management capabilities to lead the end-to-end planning, coordination, and execution of assigned deliverables. You...

Job Title: Regulatory Affairs Manager I Career Level - D Introduction to role: Join our dynamic Biopharmaceuticals R&D team as a Regulatory Affairs Manager I. This role is a unique opportunity for a regulatory specialist with project management capabilities to lead the end-to-end planning, coordination, and execution of assigned deliverables. You...

Job Title: Regulatory Affairs Manager I Career Level - D Introduction to role: Join our dynamic Biopharmaceuticals R&D team as a Regulatory Affairs Manager I. This role is a unique opportunity for a regulatory specialist with project management capabilities to lead the end-to-end planning, coordination, and execution of assigned deliverables. You...

Job Title: Regulatory Affairs Manager I Career Level - D Introduction to role: Join our dynamic Biopharmaceuticals R&D team as a Regulatory Affairs Manager I. This role is a unique opportunity for a regulatory specialist with project management capabilities to lead the end-to-end planning, coordination, and execution of assigned deliverables. You...

JOB DESCRIPTION Job Title Security specialist - Regulatory & Standards Job Description Job title: Security specialist - Regulatory & Standards Your role: As the Product Security process expert you will responsible for maintaining and enhancing the global Philips Product Security policy and process framework, driving the future...

Job TitleSecurity specialist - Regulatory & StandardsJob DescriptionJob title:Security specialist - Regulatory & StandardsYour role:As the Product Security process expert you will responsible for maintaining and enhancing the global Philips Product Security policy and process framework, driving the future strategic directions on product security...

Are you interested in working for a global company where you can work across functions and on a wide-variety of projects? As a member of Stryker's RA/QA team, that is exactly what you will do! Here, we provide our RA/QA team the opportunity to learn new things, as well as endless growth opportunities! If you are interested in working at one of the...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Department : RA CMC Diabetes & Obesity Are you passionate about what you are doing? 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...