EU Medicinal Product Manager

Job SummaryBlackfield Associates seeks an experienced Senior Regulatory Affairs professional to join their team in Slough. In this vital role, you will oversee the development and execution of regulatory strategies for medicinal products, collaborate with internal teams, and engage with regulatory authorities. Your expertise will be crucial in ensuring...

Regulatory Affairs RoleThe EU Medicinal Product Registration Specialist at Blackfield Associates will play a pivotal role in ensuring compliance with European regulatory requirements for medicinal products. This includes developing and implementing effective regulatory strategies, collaborating with cross-functional teams, and engaging with regulatory...

Job Overview:Blackfield Associates is an international pharmaceutical innovation company seeking a skilled Senior Manager Regulatory Affairs to join their EU licencing team in Slough. As a member of the team, you will play a critical role in developing and implementing regulatory strategies to bring innovative medicinal products to market. Key...

Role SummaryWe are seeking a highly experienced EU Regulatory Affairs Director to join our team at Blackfield Associates. As a Senior Regulatory Affairs Manager, you will lead our EU licensing efforts and drive regulatory strategies.About the RoleYou will be responsible for developing and implementing regulatory strategies during product development,...

The RoleWe are seeking a highly skilled Global Quality Assurance Specialist to join our team in the UK.This is an exciting opportunity for an individual looking to make a significant impact in a global pharmaceutical company as a key member of our Quality Assurance (QA) Team.Your role will involve planning, executing, and documenting quality-related...

Job OverviewWe are seeking a highly skilled Senior Regulatory Affairs Manager to join our team at Blackfield Associates. This is an exciting opportunity for a seasoned professional to lead our EU licensing efforts and drive regulatory strategies.About the RoleThe successful candidate will be responsible for developing and implementing regulatory strategies...

Company OverviewBlackfield Associates is a leading international pharmaceutical innovation company with a presence in the EU. We are seeking an experienced Senior Regulatory Affairs Manager to join our EU licensing team.About the RoleWe offer a competitive salary of £80,000 - £110,000 per annum, depending on experience, and a comprehensive benefits...

**Job Title:** Senior Manager Regulatory Affairs We are seeking a highly experienced Senior Manager Regulatory Affairs to join our EU licencing team at Blackfield Associates. This is a permanent position with hybrid working from Slough, where you will be required to attend the office on a weekly basis. About the Role:The successful candidate will develop...

Job Overview:We are seeking a dynamic Global Quality Manager / Responsible Person to join our team based in Slough, UK.The successful candidate will have a proven track record of ensuring compliance with lawful and ethical standards, as well as a strong ability to suggest improvements that benefit the organization.In addition to the estimated salary range of...

Senior Regulatory Affairs ManagerWe are seeking an experienced Senior Regulatory Affairs Manager to join our EU Licensing team at Blackfield Associates, a leading international pharmaceutical innovation company.About the Role:Develop and lead regulatory strategies throughout product development, approval, and lifecycle management.Serve as the primary point...

About the RoleWe are seeking a highly skilled Senior Quality Assurance Manager to join our team in Slough, UK.This is an exciting opportunity for an individual looking to make a significant impact in a global pharmaceutical company.As a Senior Quality Assurance Manager, you will be responsible for managing QA personnel and overseeing quality control for the...

Job Description:This exciting opportunity is for an individual looking to make a significant impact in a global pharmaceutical company, with a salary range of £60,000 - £80,000 per annum and opportunities for professional growth and development.The successful candidate will have a strong background in GMP/GDP environments, with extensive knowledge of GMP,...

Company OverviewThe international pharmaceutical innovation company Blackfield Associates is seeking a highly skilled Senior Regulatory Affairs professional to join their EU licensing team based in Slough. Job DescriptionThis permanent position involves developing and leading regulatory strategies for innovative medicinal products throughout the development,...

Compliance Expert WantedWe are searching for a Quality Management Leader to oversee our QA operations in the UK.This is a challenging opportunity for an experienced professional to take on a leadership role in our Quality Assurance (QA) Team and contribute to our growth in the global pharmaceutical market.Your primary responsibilities will include ensuring...

Job OpportunityWe are seeking an experienced Regulatory Affairs Lead to join our team at Blackfield Associates. As a Senior Regulatory Affairs Manager, you will play a key role in driving our EU licensing efforts and shaping regulatory strategies.About the JobYou will be responsible for leading the development and implementation of regulatory strategies...

Meet Our NeedsWe are seeking a skilled Pharmaceutical Compliance Manager to join our team in the UK.This is an exciting opportunity for an individual looking to make a significant impact in a global pharmaceutical company as a key member of our Quality Assurance (QA) Team.Your role will involve planning, executing, and documenting quality-related activities...

Regulatory Affairs LeadWe are recruiting a seasoned Regulatory Affairs Lead to join our EU Licensing team at Blackfield Associates, a leading international pharmaceutical innovation company.About the Job:Develop and execute regulatory strategies across product development, approval, and lifecycle management.Manage relationships with regulatory authorities...

About the Role:ClinChoice is looking for a skilled Global Regulatory Submission Lead to oversee the development and implementation of regulatory strategies for EU clinical trials. This role involves leading regulatory activities, developing regulatory strategies, and managing interactions with regulatory authorities.Key Responsibilities:– Develop and...

**Job Title:** Global Quality Assurance ManagerWe are seeking a highly skilled Global Quality Assurance Manager to join our team at ZipRecruiter. This role is an exciting opportunity for a motivated professional with experience in quality assurance and regulatory compliance.About the Role:As a Global Quality Assurance Manager, you will be responsible for...

About the CompanyUCB S.A. is a global biopharmaceutical company committed to improving patients' lives through innovative treatments and therapies. We focus on neurology and immunology, and our mission is to make a difference in the world of medicine.About the RoleThis role involves implementing local medical solutions, localizing global solutions, and...