Principal Regulatory Affairs Consultant

When our values align, there's no limit to what we can achieve.   Parexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified  Principal Regulatory Affairs Consultant (Associate Director level)  with expertise in Chemistry, Manufacturing, and Controls (CMC) for biological products and/or vaccines. The ideal candidate will...

When our values align, there's no limit to what we can achieve.   Are you passionate about regulatory affairs in the life science industry? Do you thrive in a dynamic team environment and enjoy managing complex projects? Parexel is seeking a talented Regulatory Affairs Associate to join our growing team! As a Regulatory Affairs Associate at...

When our values align, there's no limit to what we can achieve.   We are currently looking for a Senior Regulatory Affairs Consultant (Project Lead) ! As a Senior Consultant you will be responsible for leading internal projects on behalf of Parexel Clients. A Senior Consultant provides a broad range of consulting services and works within project...

When our values align, there's no limit to what we can achieve.   We are looking for a Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Procter and Gamble Polska Sp. z o.o.About the RoleThe successful candidate will be responsible for managing all regulatory activities needed to acquire Marketing Authorizations (MAs) and other authorizations for medical and non-medical products in Poland.This...

Job Title: Regulatory Affairs Associate/ManagerA competitive salary and benefits package is offered to the successful candidate.Company Overview:We are a leading multinational consumer goods company with a presence in Poland. Our team is dedicated to ensuring compliance with regulatory requirements and providing exceptional customer service.Job...

When our values align, there's no limit to what we can achieve.   We are seeking experienced Regulatory Affairs professionals to join our dynamic team in support of a global acceleration client initiative for late-stage phase III assets. This is an exciting opportunity to play a crucial role in accelerating time to filing and approval in Global Country...

Regulatory Affairs Associate/Manager47_R000119034Obowiązki Manage all regulatory activities needed to acquire Marketing Authorizations (MAs) and other authorizations for all medical and non-medical products (e.g., medical devices, food supplements, cosmetics) in Poland.Regulatory strategy: contribute to the development of the strategy by sharing...

Are you an ambitious professional looking for a challenging role in regulatory affairs? Do you have a strong background in life or natural sciences and excellent communication skills? We are seeking a highly motivated Regulatory Affairs Associate/Manager to join our team at Procter And Gamble Polska Sp. z o.o.About the RoleWe offer a competitive salary of...

You’ve picked a great time to join Avon. We’re the company that puts purpose, people and relationships at the heart of everything we do. The company that’s 135 years young and only just getting started. As part of the Natura &Co family, we’re committed to being the best beauty company for the world by generating a positive environmental, economic...

United PR z siedzibą w Warszawie to polska firma doradcza, która łączy komunikację ze strategicznym doradztwem biznesowym. W ciągu ostatnich lat do profesjonalnych usług public relations dobudowaliśmy unikalne kompetencje w obszarach corporate affairs, governmental affairs i public affairs. United PR została założona 28 lat temu jako jedna z...

We are now looking for a SENIOR REGULATORY SPECIALIST ( CTA/ IND) to join our Polish Hub. Key Responsibilities: Coordination, development, refinement of the CTA/IND lifecycle strategy, timely content & delivery appropriate to each individual regulatory agency while maintaining compliance with GSK policy and procedures. Accountable to the functional...

About the Role">This is a temporary 5-month position within our Corporate Total Reward CoE team. As Global Compensation Consultant, you will play a key role in supporting the implementation and maintenance of compensation and benefits related processes, projects, policies, and practice to ensure alignment with global guidance and market best practices.Job...

About Our ClientOur client is a multinational company with over 9,000 employees worldwide. With expertise in compliance, accounting, payroll, and corporate secretarial services, they provide their clients with guidance on local laws, regulations, and business practices.Job DescriptionThe key responsibilities of the D365 F&O Functional Consultant include...

Country Clinical LeadWarszawaNR REF.: 1190881Key Responsibilities:• Act as the local representative of the company authorized by the Managing Director, to oversee legal affairs, human resource management, regulatory intelligence and compliance, financial management, vendor identification and contracting, and business development activities within the...

Medical WriterYour responsibilities Assist in the preparation of medical and scientific documents, including manuscripts, clinical study reports, abstracts, posters, and presentations. Conduct literature searches and analyze scientific data to support content development. ...

As a Principal Software Engineer - GenAI Solutions Delivery , your primary role will be to manage the delivery of high-quality software products and features based on GenAI technology. Your expertise in software development and delivery will be the cornerstone of our success, ensuring that even without prior GenAI experience, you can lead our teams to...

About Our OrganizationWe are a global leader in innovative solutions and advanced technologies across the medical and life sciences.Job OverviewDevelop and implement quality standards, promoting a culture of excellence throughout our teams.Lead the improvement of our Quality Management System (QMS) in line with ISO 9001:2015 and ISO 13485:2016...

Job DescriptionWe are seeking a highly skilled Business Analyst to join our team at People More P.S.A. in Krakow, Poland.About the RoleThe ideal candidate will have 5+ years of experience in creating and redesigning IT processes and key controls, with a strong understanding of VAIT/DORA regulations and IT security requirements.They will also have 3+ years of...

In the role of Principal Software Engineer - GenAI Software Quality Engineering, you will be responsible for spearheading the development and implementation of testing frameworks and quality assurance processes for our GenAI services. Your expertise will be vital in creating a robust, scalable, and reliable quality engineering strategy that aligns with the...