Regulatory Affairs Professional

Job SummaryA highly skilled Regulatory CMC professional is sought to drive global regulatory strategies for innovative pharmaceutical products. This individual will lead the preparation of strategic regulatory plans, collaborate with cross-functional teams, and provide expert guidance to ensure compliance and successful product development.Key...

Regulatory Affairs Manager/Senior Manager in Global LabelingWe are seeking a highly skilled Regulatory Affairs Manager/Senior Manager to join our team at {company}. This individual will be responsible for ensuring the quality of primary and derived labeling documents, providing support for these documents, and contributing to the global labeling strategy.Key...

Regulatory Affairs SpecialistThis role involves handling Regulatory Affairs documentation related to Product Life Cycle Management (LCM) and/or New Drug Applications (NDA). It requires ensuring Regulatory Affairs compliance according to local legislation and Standard Operating Procedures (SOPs).Main Responsibilities:Prepare and submit Regulatory...

At Randstad Polska Sp. z o.o., we are seeking a highly skilled Regulatory Affairs Director to join our team. As a key member of our global regulatory affairs function, you will play a pivotal role in shaping the development and lifecycle management of our groundbreaking pharmaceutical products.Your primary responsibilities will include leading the...

We are looking for a skilled Regulatory Affairs Specialist to join our team at Randstad. The successful candidate will be responsible for ensuring compliance with regulations and interpretations of regulatory agencies.Job Description:Operational submission managementDelivery of regulatory submissions required to support product development, registration, and...

We are looking for an experienced Senior Regulatory Affairs Professional to support the implementation of regional regulatory strategies for pharmaceutical products at various stages of their lifecycle. This role involves close collaboration with global and regional teams to effectively execute regulatory submission plans, support product approvals, and...

We are seeking a highly skilled Regulatory Affairs Publishing Specialist to join our team in Warsaw, Poland.The ideal candidate will have experience in navigating complex regulatory submissions and publishing requirements, as well as excellent communication skills.Job Description:Executing the electronic publishing of moderate to complex regulatory...

ManpowerGroup Sp. z o.o., a global leader in the employment industry, is seeking a Regulatory Affairs Specialist to join their team.About UsWe are a trusted partner for businesses and individuals alike, with over 70 years of experience in providing innovative solutions for talent management.Job DescriptionThe Regulatory Affairs Specialist will be responsible...

Regulatory Affairs Specialist Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in Warsaw, Poland.Key Responsibilities:Prepare and submit regulatory documents, CTA packages, and submissions in assigned countries to ensure high quality standards.Coordinate regulatory timelines and deadlines for all assigned projects...

About ManpowerGroup Sp. z o.o.As a leading employment services company, ManpowerGroup Sp. z o.o. has a long history of providing job seekers with new opportunities and professional guidance. With a presence in 82 countries and nearly 35 locations across Poland, we strive to help individuals find meaningful work that matches their skills and experience.Job...

Polpharma S.A. is a leading pharmaceutical company that seeks a highly skilled professional to fill the position of CHC Regulatory Affairs Team Head. In this role, you will lead our CHC regulatory affairs team, providing strategic guidance on registration strategies and ensuring compliance with relevant regulations.Key Responsibilities:Team Leadership:...

**Job Title:** Manager, Regulatory AffairsContribute to Global Development and Lifecycle ManagementYou will lead the development and execution of global CMC regulatory strategies, ensuring compliance with regulatory requirements and representing Global CMC Regulatory Affairs in cross-functional and external collaborations.About This Opportunity:This is an...

For our Client, one of the biggest Pharmaceutical Companies worldwide, we are looking for a Regulatory Affairs Senior / Specialist in Submission Publishing who will be responsible for executing the electronic publishing of complex regulatory submissions for national, regional and global regulatory agencies and operating companies in both eCTD and non-eCTD...

We are seeking a highly skilled Regulatory Affairs Manager to lead the development and maintenance of primary labeling for assigned compounds. This role requires strong leadership skills, as well as expertise in pharmaceutical regulatory guidelines.Key Responsibilities:Develop and maintain primary labeling documentsEnsure compliance with worldwide regulatory...

Role OverviewWe are seeking a highly skilled Regulatory Affairs Expert to join our team at Randstad Polska Sp. z o.o.The successful candidate will be responsible for ensuring compliance with regulations and interpretations of regulatory agencies in the pharmaceutical industry.This is an exciting opportunity for a motivated individual to contribute to the...

About the RoleWe are seeking a Senior Regulatory Specialist, CTA/IND to join our Polish Hub.Key Responsibilities:Develop and implement regulatory strategies for CTA/IND submissions, ensuring compliance with GSK policy and procedures.Collaborate with cross-functional teams to achieve project goals and deliver high-quality results.Manage and maintain accurate...

We are seeking a highly skilled Regulatory Affairs Submissions Specialist to support our client specialized in pharma industry.About the ClientThe client is a global leader in the pharma industry, with a presence in over 70 countries and a portfolio of products that includes both prescription and over-the-counter medications.Job SummaryThe Regulatory Affairs...

At ManpowerGroup Sp. z o.o., we are a global leader in the employment industry, operating in 82 countries and serving clients across various industries.Job OverviewWe are seeking a Regulatory Affairs Publishing Specialist to join our team, who will be responsible for executing electronic publishing of regulatory submissions for national, regional, and global...

We are seeking a seasoned Global Regulatory Affairs Specialist to join our team at Randstad. In this role, you will be responsible for managing the operational delivery of regulatory documents for product registration and compliance. Your expertise will help us ensure that all regulatory requirements are met, and our products reach the market...

ManpowerGroup Sp. z o.o., a global leader in the staffing industry, is seeking a highly skilled Regulatory Affairs Submissions Specialist to join our team.About the JobWe are recruiting for a Regulatory Affairs Professional Submission Specialist (Mid and Senior position) to support our client specialized in pharma industry.Job DescriptionThe Experienced RA...