Regulatory Affairs Professional

Are you looking for a challenging opportunity in the pharmaceutical industry?Randstad Polska is seeking an ERMC Specialist to join our international Regulatory Affairs Team.We offer:A 12-month employment contract with the possibility of extensionHybrid work arrangement (2 days a week remote work)A comprehensive benefits package, including medical care,...

Unlocking the Potential of Regulatory Affairs ExpertsParexel, a leading Clinical Research Organization (CRO), is seeking an experienced Principal Regulatory Affairs Consultant (Associate Director level) to join our team. The ideal candidate will possess strong regulatory affairs experience, project management skills, and in-depth knowledge of post-approval...

Parexel is seeking a highly qualified Regulatory Affairs Expert to lead post-approval Chemistry, Manufacturing, and Controls (CMC) activities for small molecule projects.The ideal candidate will possess strong regulatory affairs experience, project management skills, and in-depth knowledge of CMC regulations. As a recognized professional in your field of...

Company OverviewWe are seeking a highly skilled Regulatory Affairs Expert to join our international team.Job DescriptionIn this role, you will be responsible for coordinating lifecycle management procedures, ensuring timely submissions of high-quality dossiers, and managing validation issues. You will also work closely with colleagues to complete databases...

Parexel Consulting is a leading pharmaceutical industry expert seeking a highly skilled and experienced CMC Regulatory Affairs Professional to join our team as a Regulatory Affairs Consultant.Job OverviewThe ideal candidate will possess exceptional communication skills, strong writing experience, and in-depth knowledge of CMC regulations, including EMA...

Job Summary: Manpower (Agencja zatrudnienia nr 412) is a global company with over 70 years of experience, operating in 82 countries. We have been on the Polish market since 2001 and currently have almost 35 branches across the country. Our goal is to open up new opportunities for candidates, help them find a job that matches their qualifications and...

Parexel: A Global Leader in Clinical ResearchWe are seeking an experienced Regulatory Affairs professional 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 emerging markets and non-EU markets.Our...

Parexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Regulatory Affairs Expert to join their team.The ideal candidate will possess strong regulatory affairs experience, project management skills, and in-depth knowledge of post-approval requirements. As a recognized professional in your field of expertise, you will utilize...

Unlock Your Potential in Medical ScienceBoston Scientific, a leader in medical science for over 40 years, offers an exciting opportunity for a Regulatory Affairs Specialist to join our team. With a deep commitment to advancing science for life, we're looking for a skilled professional to help us tackle the challenges that matter most.About the Role:This is...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our international team at Randstad Polska. This role involves working closely with our clients in the pharmaceutical industry, providing expertise in regulatory affairs data management.Company OverviewOur client is an international company from the pharmaceutical industry,...

Job OverviewParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Senior Regulatory Affairs Specialist to join our team. This role offers a unique opportunity to utilize your technical skills and specialist knowledge to deliver exceptional consulting services to our clients.About the RoleWe are looking for an experienced...

About the RoleAs a Regulatory Affairs Expert - CMC Product Registration, you will be responsible for managing multiple CMC new files and CTA assignments for Pharma, Biopharm, and Vaccines products. Your primary focus will be on ensuring compliance with Company regulatory processes and external requirements.Key ResponsibilitiesDefine and agree regulatory...

Parexel's MissionWe are a leading global biopharmaceutical solutions organization committed to supporting our clients in bringing innovative treatments to market. Our expertise spans the entire product development cycle, from clinical trials to commercialization.Job SummaryWe are seeking an experienced Regulatory Affairs professional to join our dynamic team...

About the Role:We are seeking a highly skilled Senior Regulatory Affairs Specialist, Chemistry Manufacturing and Controls to join our team at GSK. The successful candidate will be responsible for ensuring that our pharmaceutical and vaccine products are safe, effective, and of high quality for patient use.Key Responsibilities:Manage multiple CMC new files...

We are seeking a highly skilled and experienced Senior Pharmacovigilance Expert to join our team in EU Regulatory Affairs. As a key member of our Global Patient Safety team, you will play a critical role in ensuring the safety of our medicines and complying with European regulatory requirements.

Parexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Regulatory Affairs Consultant with expertise in Chemistry, Manufacturing, and Controls (CMC) for biological products and/or vaccines. As a recognized professional in your field of expertise, you will utilize your skills to deliver exceptional consulting services to our...

About the RoleWe are seeking a skilled Regulatory Affairs Specialist to join our team at 9605 GSK Services Sp z o.o. in Poland.Job DescriptionThis is a dynamic and challenging role that requires strong communication skills, attention to detail, and the ability to work effectively in a matrix environment.The successful candidate will be responsible for...

Job Description:Parexel Consulting seeks a highly skilled Regulatory Affairs Specialist to lead the preparation and submission of CMC components for investigational new drugs, marketing authorizations, and other regulatory submissions.In this role, you will collaborate closely with a multinational pharmaceutical company, ensuring the effective planning,...

About the RoleParexel Consulting is seeking a skilled Regulatory Affairs Consultant to join our team. As a key member of our multinational pharmaceutical company, you will play a crucial role in ensuring the effective planning, review, and preparation of CMC components for investigational new drugs, new drug license applications, progress reports,...

About the RoleGlovo is seeking a seasoned Corporate Affairs expert to spearhead our Public Affairs and Communications efforts in Poland.This is a unique opportunity to join a fast-paced, dynamic company that is revolutionizing the way people connect with their everyday needs.We're looking for a strategic thinker who can develop and implement a unified...