emplois telix pharmaceuticals emea
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12 emplois
- Telix Pharmaceuticals LimitedLiègeAnnonce·
- 3+ years of regulatory affairs experience in the pharmaceutical industry required.
- Prepares, reviews, analyses, and consolidates all relevant pharmaceutical and…
- Telix Pharmaceuticals (EMEA)Travail hybride à Seneffe·
- 4 years of experience in supply chain activities as Warehouse Operator in GMP environment, ideally in the pharmaceutical field.
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Seneffe » ou Emploi Warehouse Worker - Seneffe »
- Rechercher les salaires : Warehouse Operator
- Telix Pharmaceuticals (EMEA)Travail hybride à Liège·
- 5+ years of proven experience in pharmaceutical and packaging processes (preferably secondary packaging).
- Bachelor's degree in engineering (e.g. in chemical,…
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Liège » ou Emploi Process Engineer - Liège »
- Rechercher les salaires : Manufacturing & Process Engineer EMEA
- Telix Pharmaceuticals (EMEA)Travail hybride à Liège·
- 3+ years of regulatory affairs experience in the pharmaceutical industry required.
- Prepares, reviews, analyses and consolidates all relevant pharmaceutical and…
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Liège » ou Emploi Regulatory Affairs Specialist - Liège »
- Rechercher les salaires : Specialist, Global Regulatory Affairs - Liège
- Telix Pharmaceuticals (EMEA)Travail hybride à Seneffe·
- As a RadioProtection Officer (RPO) at Telix, you will oversee operations related to radiation protection within the facilities (radiopharmacy part and cyclotron…
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Seneffe » ou Emploi Protection Officer - Seneffe »
- Rechercher les salaires : Radioprotection Officer
- Telix Pharmaceuticals (EMEA)Travail hybride à Seneffe·
- Operating within a highly regulated environment, you will adhere to stringent safety and quality standards to uphold operational excellence and industry…
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Seneffe » ou Emploi Technician - Seneffe »
- Rechercher les salaires : Cyclotron Technician
- Telix Pharmaceuticals (EMEA)Travail hybride à Liège·
- Maintain a high level of team knowledge of and appropriately implement current local pharmaceutical regulation and ensure implementation of Telix policies and…
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Liège » ou Emploi Liaison - Liège »
- Rechercher les salaires : Senior Medical Science Liaison (International)
- Telix Pharmaceuticals (EMEA)Travail hybride à Seneffe·
- Develop drug production processes that comply with safety standards and pharmaceutical quality.
- Telix is seeking applicants for a Radiochemist position.
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Seneffe » ou Emploi Chemist - Seneffe »
- Rechercher les salaires : Radiochemist
- Telix Pharmaceuticals (EMEA)Travail hybride à Seneffe·
- Additionally, you will be responsible for building and managing the Radioisotopes Production team, including overseeing their work and professional development.
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Seneffe » ou Emploi Production Manager - Seneffe »
- Rechercher les salaires : Radioisotopes Production Manager
- Telix Pharmaceuticals (EMEA)Travail hybride à Liège·
- 10+ years of relevant radiopharmaceutical/pharmaceutical/biopharma CMC experience with 5+ years of CMC program/project management experience.
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Liège » ou Emploi Program Leader - Liège »
- Rechercher les salaires : CMC Program Lead - TLX599CDx & Scintimun
- Telix Pharmaceuticals (EMEA)Travail hybride à Liège·
- The Global Clinical Lead will ensure the renal cancer therapeutic programs are founded on sound scientific decision-making and are able to be progressed…
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Liège » ou Emploi Clinical Lead Nurse - Liège »
- Rechercher les salaires : Global Clinical Lead, Renal Cancer Therapeutics
- Telix Pharmaceuticals (EMEA)Travail hybride à Liège·
- 10+ years of relevant radiopharmaceutical/pharmaceutical/biopharma CMC experience with 5+ years of CMC program/project management experience.
- Voir toutes les offres de type « Emploi Telix Pharmaceuticals (EMEA) », « Liège » ou Emploi Program Leader - Liège »
- Rechercher les salaires : CMC Program Lead - TLX66 & TLX592
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Job Post Details
Specialist, Global Regulatory Affairs - job post
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Description du poste
See Yourself at Telix
Telix is currently seeking a Specialist to join our Global Regulatory Affairs team in Europe. This position is responsible for the preparation and the execution of the regulatory strategy and dossier compliance for dedicated products in the EMEA region.
Key Accountabilities:
- Prepares and executes, in collaboration with other regulatory affairs team members, global regulatory strategies and submission requirements pertaining to assigned projects in line with Telix’s objectives and initiatives.
- Represents regulatory affairs on project teams as a subject matter expert by providing guidance and regulatory expertise to other departments in support of product development and product life-cycle management.
- Interacts with appropriate national/regional regulatory agencies.
- Prepares, reviews, analyses, and consolidates all relevant pharmaceutical and related technical information required for regulatory dossier submission of the company's drug products with regulatory agencies (including but not limited to MA transfer, variation, and renewal applications).
- Provides regulatory expertise for the EMEA region.
- Monitors EMEA health authority regulations, guidelines, and specifications to maintain regulatory submission compliance.
- Performs any other regulatory tasks assigned by the manager.
Education and Experience:
- Undergraduate degree with a focus in life sciences required.
- 3+ years of regulatory affairs experience in the pharmaceutical industry required.
- Experience in EU regulatory affairs is a must.
- Experience in centralized procedures, MA transfer, life-cycle management is a must.
- Experience in UK and Swiss procedures is a plus.
- Experience in radiopharmaceuticals and/or oncological products is a plus.
- Good written and verbal communication skills in English.
Key Capabilities:
- Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected.
- Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges.
- Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do.
- Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results.
- Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders.
- Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges.
- Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language.
- Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals.
- Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges.
- Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills.
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