Quality and Regulatory Documentation Administrator

Quality and Regulatory Compliance Administrator CEELocation: Warsaw, Salsy (POL), Masovia, PL - PolandEmpowering careers at ARJOAt Arjo, we know what moves us. We go above and beyond for people facing mobility challenges. We take every opportunity to work and grow as one team and take pride in sharing our knowledge and experience. Does that sound like...

Senior Quality and Regulatory Affairs Specialist page is loadedSenior Quality and Regulatory Affairs SpecialistApply locations POL - Warsaw time type Full time posted on Posted 30+ Days Ago job requisition id R79316Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.At Smith+Nephew we are looking for: Senior...

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.At Smith+Nephew we are looking for: Senior Quality and Regulatory Affairs SpecialistWhat will you be doing?Coordinate product handling activities including value-added services between the legal manufacturer and the third-party logistics provider with a...

Senior Quality and Regulatory Affairs Specialist, WarsawClient:Smith+NephewLocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:b95c2bd88f5fJob Views:4Posted:19.04.2025Expiry Date:03.06.2025Job Description:Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.At Smith+Nephew we are...

The Senior Quality and Regulatory Affairs Specialist role at Smith+Nephew offers a unique opportunity to work with a leading medical technology company that is passionate about improving patient outcomes. In this role, you will be responsible for ensuring the quality and regulatory compliance of our medical devices, working closely with cross-functional...

Job Title: Compliance and Regulatory ExpertJob Description:The Compliance and Regulatory Expert will be responsible for providing guidance on trade regulations and laws to ensure Mars' compliance. This position will work closely with various departments to ensure accuracy and consistency in regulatory compliance.Key Responsibilities:Conduct regular audits of...

Job OverviewThe Principal Medical Writer role at GlaxoSmithKline involves preparing and reviewing clinical documents to ensure compliance with regulatory requirements.Key Tasks:Develop and review clinical regulatory documents, including protocols, study reports, and CTD submissions.Collaborate with cross-functional teams to ensure timely delivery of clinical...

About the JobThis is a site-based role requiring a high level of verbal and written English skills.As a Document Controller, you will work closely with the engineering team and support them with actions such as closing RFIs and reviewing project documentation.Additional duties may include knowledge sharing applications and experience with Asite and Viewpoint...

**About the Role**In this position, you will be working as a Technical Documentation Expert, responsible for creating high-quality technical documentation for our medical devices.Key Responsibilities:Preparing technical documentation for IVDs & FDA various risk classes.Assisting in post-marketing surveillance activities.Participating in compliance / QMS...

We're looking for a skilled Clinical Documentation Lead to lead our clinical documentation team.The ideal candidate will have extensive experience in completing multiple-document projects, including functioning as the lead medical writer for a CTD submission dossier with authoring and oversight activities across several Module 2 documents.Key...

Quality Assurance Regulatory Affairs Analyst for Beckman Coulter DiagnosticsBeckman Coulter Diagnostics is responsible for QRA processes support for all EE countries (PL, CZ, SK, HU and CRO). This position is part of the Department of Quality and Regulatory located in 4 EE countries and will be Hybrid.You will be responsible for sustaining and continually...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.Join Our Team as a Senior Quality Administrator - hybrid in...

Bacteromic is an innovative medical diagnostics company that's changing the way healthcare professionals diagnose and treat bacterial infections. As a Technical Documentation Manager, you'll play a vital role in ensuring that our products meet the highest standards of quality and safety.Your responsibilities will include:Developing and maintaining technical...

About the RoleAt TN Poland, we are seeking a highly skilled Senior Regulatory Specialist, Country Labeling to join our team. This is an exciting opportunity for a talented professional to lead our regional/country labelling efforts and ensure timely update, management, and communication of quality regional and local labeling/Product Information (PI) and...

Regulatory Data and Conformance ManagerWhy Patients Need YouWe're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise...

Key ResponsibilitiesYou will provide guidance to operational teams for managing projects and prepare forecasts for resource requirements.You will assess all Quality events received within Worldwide Strategy and Regulatory as described in Quality Management System.You will ensure transparency and excellence in evaluation, definition, and execution of...

About the RoleWe are seeking a highly skilled Clinical Document Specialist to join our team. As a Clinical Document Specialist, you will be responsible for developing and maintaining high-quality clinical documents, including protocols, clinical study reports, and regulatory submissions.Key Responsibilities:- Develop and maintain technical documentation,...

Your Opportunity at PerrigoWe are looking for a highly motivated Regulatory Affairs Associate to join our medicines team. As a member of our team, you will play a key role in supporting life cycle maintenance activities in medicinal portfolios across the EU, ensuring compliance with legislative frameworks and internal policies.This role offers a unique...

About Our TeamThe CMC Regulatory Affairs group at GSK ensures the approval and continuous supply of medicines. This team brings together operation and execution aspects for key regulatory deliverables.Key ResponsibilitiesThis position involves managing multiple CMC new files and CTA assignments, defining regulatory strategy, and delivering high-quality...

**Job Overview**We are looking for a Quality Assurance Professional to join our team. In this role, you will be responsible for ensuring the quality of our technical documentation and compliance with regulatory requirements.Key Responsibilities:Ensuring the accuracy and completeness of technical documentation.Participating in post-marketing surveillance...