Ra-Cmc Specialist

With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries.We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology market through Injectable...

Galderma is a pioneering dermatology company with a rich legacy and commitment to innovation. With operations in approximately 90 countries, we deliver a diverse portfolio of premium brands and services that cater to the evolving needs of the dermatology market.We are seeking an expert Regulatory Affairs CMC Specialist to join our team in Barcelona. As a key...

Job Summary:The Junior Manager, Regulatory Affairs CMC is responsible for providing regulatory relevant technical assistance to development teams and ensuring the adequacy of CMC documentation for global regulatory submissions, including specific requirements for regional registration processes.This role supports and promotes all regulatory CMC tasks...

Parexel, a leading Clinical Research Organization (CRO), is committed to empowering our clients with exceptional consulting services. We are seeking an experienced Principal Regulatory Affairs Consultant (Associate Director level) to join our team. This role offers the opportunity to showcase your expertise in Chemistry, Manufacturing, and Controls (CMC) for...

About the Role:We are seeking a highly skilled CMC Regulatory Manager to join our team at Parexel. As a key member of our regulatory affairs team, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.Key Responsibilities:Develop...

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Alk-Abelló A/S. As a world leader in allergy, our aspiration is to provide options for prevention, diagnosis, and treatment of allergy, helping as many people as possible to a better life.Key responsibilities include handling regulatory CMC documentation for products...

Job Summary: We are seeking a highly skilled Senior Quality Assurance Specialist to join our remote QA/RA team based in several European countries. As a key member of our team, you will play a critical role in ensuring compliance with quality and regulatory requirements for our medical devices.Key Responsibilities:Lead complaints investigation and manage...

Job DescriptionThis is a highly specialized role for an experienced Regulatory Affairs professional, with expertise in biopharmaceuticals and biosimilars. You will be responsible for ensuring the adequacy of CMC documentation for global regulatory submissions, including regional registration processes.The ideal candidate will have broad knowledge of global...

Cell Line Development Specialist OpportunityWe are seeking a highly skilled Cell Line Development Specialist to join our multidisciplinary team at HIPRA. As a key member of our R&D Department, you will play a crucial role in managing our cell culture unit and performing hands-on cell line development activities for biopharmaceutical use.About the RoleThe...

Job Summary:We are seeking a skilled Regulatory Compliance Specialist to join our team at Vision Achievement. As a key member of our life sciences team, you will be responsible for providing expert guidance on regulatory and quality assurance infrastructure, ensuring compliance with relevant regulations and standards.In this role, you will conduct thorough...

Job Title: Operational Technology SpecialistJob Summary:We are seeking a skilled Operational Technology Specialist to join our team at Fortinet. The ideal candidate will have hands-on experience in Operational Technology / Industrial Control Systems / Supervisory Control and Data Acquisition environments and strong understanding of DNS and NFS, SMTP, HTTP,...

About the RoleWe are seeking a talented R&D Scientist to join our multidisciplinary team at HIPRA. As a Cell Line Development Specialist, you will be responsible for managing a cell culture unit to perform hands-on cell line development activities for biopharmaceutical use.Key Responsibilities- Transfection, selection, subcloning, clone screening, cell...

Job Title: Operational Technology Systems SpecialistJob Summary:We are seeking an experienced Operational Technology Systems Specialist to join our team at Fortinet. The successful candidate will have a strong background in Operational Technology and Industrial Control Systems, with a proven track record of delivering successful security solutions.Key...

Job Title: Regulatory Affairs SpecialistThe Regulatory Affairs Specialist at Zentiva Group, a.s. is accountable for managing the Regulatory Affairs agenda at country level. This includes providing an efficient and proactive Regulatory service to meet business objectives, supporting commercialization of products, ensuring agility in daily interaction with...

About Moderna TherapeuticsModerna is a pioneering biotechnology company at the forefront of developing groundbreaking mRNA technologies to revolutionize medicine. Our diverse pipeline of development programs is transforming the pharmaceutical industry.Job DescriptionWe are seeking a highly skilled Senior mRNA Technology Specialist to support our technical...

The Clinical Research Associate Specialist at Parexel plays a crucial role in the start-up phase of clinical trials. This position involves performing all study start-up activities, from site identification to pre-initiation. The specialist will be responsible for managing and driving the strategy for the Pre SIV/start-up tasks of the study, ensuring quality...

Regulatory Affairs SpecialistJohnson and Johnson is seeking a skilled Regulatory Affairs Specialist to join our team in Madrid. This role offers a hybrid working model and is an exciting opportunity to contribute to our company's mission to build a world where complex diseases are prevented, treated, and cured.Key ResponsibilitiesSupport the growth of our...

.(Senior) Specialist Regulatory Affairs/Start-upErgomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease.Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia.Our company allows...

.(Senior) Specialist Regulatory Affairs/Start-up Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease.Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia.Our company allows...

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