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,...

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...

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...

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...

Manpower (Agencja zatrudnienia nr 412) to globalna firma o ponad 70-letnim doświadczeniu, działająca w 82 krajach. Na polskim rynku jesteśmy od 2001 roku i obecnie posiadamy prawie 35 oddziałów w całym kraju. Naszym celem jest otwieranie przed kandydatami nowych możliwości, pomoc w znalezieniu pracy odpowiadającej ich kwalifikacjom i...

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...

When our values align, there's no limit to what we can achieve.   Parexel, a leading Clinical Research Organization, is seeking a Regulatory Affairs Associate (Labelling) to join our team. As a Regulatory Affairs Associate, you will be responsible for managing and coordinating text and artwork changes, ensuring compliance with regulatory requirements...

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,...

When our values align, there's no limit to what we can achieve.   Job Description Parexel Consulting is seeking a talented and experienced CMC Regulatory Affairs Professional to join our team as a Regulatory Affairs Consultant. In this role, you will have the opportunity to utilize your expertise in CMC, exceptional communication skills, and strong...

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...

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 small molecule. The ideal candidate will possess strong...

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...

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...