Senior Regulatory Specialist

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...

Job OverviewThe Senior Regulatory Specialist, Country Labelling is a key role within TN Poland, responsible for ensuring the effective coordination, communication, and maintenance of regional/country labelling documents. This position requires strong leadership skills to provide support to global and local GRA team members.Key Responsibilities:Authoring and...

TN Poland is seeking an experienced Senior Regulatory Specialist to join our team. As a key member of our CMC team, you will be responsible for supporting global CMC regulatory strategies and documentation.We are looking for someone with first-hand experience in CMC or other regulatory affairs areas and a university degree in Life Sciences or a related...

Job DescriptionGSK is a global biopharma company with a mission to unite science, technology, and talent to get ahead of disease together. As a Senior Regulatory Specialist, you will play a critical role in ensuring the lifecycle of GSK products complies with regulatory requirements.Key Responsibilities:Manage multiple CMC variations and source transfers of...

Job Description:We are seeking an experienced Junior Regulatory Specialist to join our Compliance Risk Management team at Citigroup Inc.This is an exciting opportunity for a highly skilled professional to contribute to the development of regulatory strategies and initiatives.About the Role:As a Junior Regulatory Specialist, you will assist in analyzing and...

TN Poland is committed to maintaining the highest standards of corporate governance and risk management. We are seeking a talented Risk Management Professional to join our team and contribute to our efforts to mitigate risks and ensure regulatory compliance.Key Responsibilities:Develop and implement effective risk management strategies to identify and...

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...

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...

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...

About the RoleWe are seeking a skilled Regulatory Compliance Specialist to oversee our global compliance operations, ensuring adherence to regulatory requirements across multiple jurisdictions.The ideal candidate will have a deep understanding of financial regulations and global licenses, as well as strong leadership skills to manage a team.Develop and...

About the OpportunityWe are seeking a Senior Regulatory Specialist, CTA/IND to join our Polish Hub.Responsibilities:Develop and implement regulatory strategies for CTA/IND submissions.Collaborate with cross-functional teams to achieve project goals.Manage and maintain accurate records of regulatory submissions and communications.What You'll Get:Competitive...

TN Poland is seeking a highly qualified Principal Regulatory Affairs Consultant to join their team in Warsaw. The successful candidate will possess strong regulatory affairs experience, project management skills, and in-depth knowledge of post-approval Chemistry, Manufacturing, and Controls (CMC) activities.This is a unique opportunity for a highly qualified...

Role OverviewThe Regulatory Specialist will be responsible for the development and management of Pharmacovigilance Risk Management Plans (PV-RMPs) to support drug and biologic products.This position is part of the Risk Management function within the organization, responsible for facilitating cross-functional review and approval of PV-RMPs.The ideal candidate...

About the JobWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Innovaderm. As a key member of our regulatory department, you will be responsible for ensuring compliance with applicable EU regional regulations and guidelines.The ideal candidate will have a strong background in clinical research, excellent knowledge of GCP and...

About the RoleWe are seeking an experienced Regulatory Specialist to join our team in TN Poland. The successful candidate will be responsible for ensuring the accuracy and compliance of regional/country labelling documents.Main Tasks:Compiling market-specific supporting documentation for labelling submissions in accordance with regulatory authority...

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...

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...

About the PositionSQUARE ONE RESOURCES sp. z o.o. is looking for a highly skilled Regulatory Affairs Specialist to join their team. The successful candidate will be responsible for drafting and reviewing contractual documents related to digital solutions, including Subscription Agreements, Services Agreements, License Agreements, Data Processing Agreements,...

Job DescriptionWe are seeking a highly motivated and detail-oriented Regulatory Compliance Specialist to join our dynamic team. The ideal candidate will be responsible for monitoring and ensuring compliance with global financial licenses and regulations. This role requires an individual who is proactive in staying updated with regulatory changes and can help...

Our client is a leading pharmaceutical company seeking an experienced Regulatory Affairs Publishing Specialist to join their team.The successful candidate will be responsible for executing the electronic publishing of moderate to complex regulatory submissions for national, regional, and global regulatory agencies and operating companies in both eCTD and...