On-site jobs in Austria (2), Belgium (12), Bulgaria (1), Croatia (1), Cyprus (1), Denmark (8), France (12), Germany (18), Greece (6), Hungary (1), Ireland (24), Italy (7), Malta (2), Multiple Countries (17), Netherlands (14), Poland (9), Portugal (3), Romania (3), Spain (5), Sweden (3), Switzerland (13) and United Kingdom (25).
Serving as the primary QP at ATI for aseptically manufactured, parenteral products. Coaching and mentoring quality colleagues to develop problem-solving, decision-making, and...
This role serves as a close business partner and facilitator of regulatory activities and is expected to contribute to developing sound regulatory strategies globally. The role...
The activities of your team will concentrate on the identification of novel therapeutic concepts in immune regulation and tolerance with the potential to lead to transformative...
This position provides strategic oversight of PV quality systems, audits, and inspections while ensuring compliance with global and regional regulatory requirements. The individual...
Provide European regulatory strategy support for assigned projects, products and non-project work. Act as a specialist in the area of oncology. Represent Regulatory Affairs...
The primary responsibilities will include design control activities, new product development, and executing tasks related to maintaining our current products. Protein purification...
Acts as Single Point of Contact/SPOC for all quality related activities at the External Supplier and establishing good working relationships with clear communication and defined...
This position is responsible for working with the physicians and other clinical scientists within Early Clinical Development to provide clinical research support for early phase...
Conduct protein analysis with use of Mass Spectrometry based methods, e.g peptide mapping, disulphide bridges mapping, post translational modifications, intact mass profiling etc...
You will oversee data management activities associated with clinical drug development for all clinical trials in Ascendis’ rare endocrinology portfolio. Furthermore, the duties...
Develop and maintain the highest scientific and medical knowledge in the relevant fields and be acknowledged internally and externally as an expert and provide medical support to...
Plan and design own experiments for development of downstream processes for therapeutic proteins. Design and execution of high throughput chromatography methods. Ensure that...
Oversee and guide various programs from H2L to IND program utilizing multiple modalities including small molecules, ASOs, and biologics. Lead multiple project teams in a matrix...
Responsible for ensuring compliance with global regulatory requirements, development of compliance reports/metrics and implementation of corrective/preventative actions to address...
Supervise and execute pharmaceutical processing activities to achieve operational objectives and provide daily updates on operational status. Lead and facilitate safe and effective...
Responsible for establishing governance and defining standards for interactions with third party business partners in pharmacovigilance and for coordinating PV provisions for the...
Perform qualitative and quantitative analyses of compounds, including drug substances, drug product intermediates and drug product; Recommend the analytical characterization...
Accountable for new business generation, sales growth and customer acquisition where you will be supplying products into three clearly defined markets; Life Sciences...
You lead a team of research associates and scientists dedicated to developing and validating (bio)assays for release and stability testing of antibody products. You will focus on...
Lead Scientific Strategy: Direct the scientific strategy for the project within Global Antigen Design, operating within a fast-paced and agile environment to drive innovation and...
Performing a range of analytical experiments using different separation and characterisation methods (IEC, SEC, RP, HIC, HILIC, CE-SDS, LC-MS and LC-MS/MS); Experience in...
You will be key in leading a team (10-15 HC) of highly talented scientists and researchers in a matrix organization. You will shape, support, develop and optimize the team...
Provide visionary leadership for the Quality Control function, defining and executing the strategic direction for quality control activities across the Aachen Site, being Part of...
Write and review clinical (and nonclinical) documents for regulatory submissions in the EU and US, such as Module 2.5, 2.7, 2.4, 2.6, integrated summaries of efficacy/safety...
This pivotal role is responsible for delivering an effective testing and analytical service to ensure that our plant's products consistently meet specified standards. As an...
Lead and mentor a team of Analytical Subject Matter Experts for both biologics and small molecule drug products fostering innovation and technical excellence; Support the...
Lead the creation and execution of global brand plans for our microbiology range globally, and for all market segments, from developing to developed settings, ensuring alignment...
You will be responsible for the comprehensive execution and oversight of the Product Development Process (PDP) for a given project within our R&D group. In the role, you will drive...
The role will provide leadership and strategic direction for assigned programs, ensuring the successful implementation of the quality strategy and/or quality plans to foster a...
Are you an experienced Regulatory Affairs leader with a passion for medical devices? Are you looking for a motivated and diverse department to empower, guide and mentor Applied...
Contribute to study protocol development including study concept, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate,...
You will support the professional development of their reports, ensure that robust Medical Affairs plans are developed and executed on time, on budget, and to strategy, and foster...
Develops a strategy for external manufacturing of Teva’s products and manage its implementation, in collaboration with TGO leadership and commercial units. Establishes and...
This role is pivotal in driving biomarker strategies, early clinical development plans, and providing scientific expertise and strategic guidance. The successful candidate will...
Lead and provide technical expertise in the planning and execution of IVD assay development projects, acting as a knowledge expert for quantitative PCR (qPCR) diagnostic systems...
You will provide leadership for all Small Molecule QC laboratories related to Lonza’s Visp site. You will ensure adequate resources (staff, laboratory and instrumentation) to...
As part of our PV team you will be working collaboratively with the Global Product Safety Science Lead (GPSSL) for assigned product(s) as well as with other PV functions, to ensure...
Responsible for the planning and organization of formulation and process development of various modalities - with a focus on parenteral formulation containing nanoparticular...
Lead (Co-lead) the study teams to develop a cross-functional, integrated study implementation plan including creation of initial study budget, study kick-off and team meetings....
A managerial position responsible to ensure that assigned Quality Management System activities are managed in compliance with regulations and company policies and in accordance...
The core responsibility of the Medical Director is to lead the local medical department, be a part of pan-European R&D projects and work closely with other medical departments in...
As a successful candidate, you will take the role of Team Leader In vitro Laboratory a team of 2-4 scientists engaged in drug discovery projects for biotech and pharma companies...
In this role, you will lead a team of five quality officers, providing direction and coaching to elevate both the quality of work and the motivation of your team. We are seeking a...