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QA Specialist og Senior QA Specialist
For dig, der trives med at arbejde med kvalitet og lovgivning fra et operationelt perspektiv, både selvstændigt og i dialog med vores leverandører og interne afdelinger.
Som QA Specialist vil du være det koordinerende bindeled mellem de forskellige teams i QA, regulatorisk og Pharmacovigilance i relation til udfærdigelse eller opdatering af eksisterende TA.
Senior Technical Writer - Regulatory (CMC)
You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.
Stepping into an informal and collaborative environment, you will have close interfaces with many different disciplines, including Global Pharmaceutical R&D, manufacturing sites, Product Supply, Quality Assurance, Ferring affiliates, and development sites around the world.
MS&T Program Manager
We are looking for an experienced professional from the pharmaceutical industry, who can effectively manage project plans across multiple entities and lead cross-functional processes within our own sites and supply chain.
As a MS&T Program Manager, you will be responsible for managing the projects, maintaining project databases, as well as ensuring effective communication and timely achievement of milestones.
Manufacturing Science & Technology (MS&T) Technical Transfer Project Manager (Sr Specialist)
Join Orifarm and take charge of building strong business relationships with a key portfolio of our suppliers!
As a MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to Supplier Relationship Management functions, and manufacturing sites comprising support, technological transfers between CMOs and own manufacturing sites, analytical method development and validation, external product development at CDMOs and driving continuous technological improvement and innovation.
Protein Chemist for production of antibodies for cancer diagnostics
Do you find antibody production exciting?
You will play a key role in daily support of the production of conjugates. This can include:
- Support lab techs in case of technical issues with purification, conjugation, and test of antibodies.
- Handle compliance issues according to GMP standards.
We offer a high degree of freedom and development opportunities in an international company.
CTS Proposal Manager
Join an international drug development consultancy and contribute with strategic advice and operational support to clients based in Europe, the US and Asia.
You will be part of a dedicated proposal team adding unique and highly valued competencies to the proposal process in CTS, supporting and underlining our professional cooperation with present and future clients in all parts of the world.
Our Proposal Managers work closely together with all parts of the organisation and represents the anchor of our client dialogue both in initial phases and as support throughout the client-life-cycle.
Quality Control Manager med sans for optimering og rapportering
Kan du med dit store kendskab til kvalitetskontrol i fødevarebranchen etablere og vedligeholde en effektiv overvågning, analyse og rapportering af kvalitetsområdet?
Virksomheden sælger en bred vifte af fødevarer, blandt andet honning, marmelader, saucer, dressinger samt nødder, kerner og frø. Du kommer til at sikre og videreudvikle effektive kvalitetskontroltests på råvarer, mellemprodukter og færdigvarer.
Clinical Supply Manager
The Clinical Supply Manager will be managing outsourcing of packaging, labelling, and distribution of clinical trial supplies for all clinical trials.
You must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.
We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.
Clean Utility Engineer
Are you ready to be a part of Novo Nordisk's most significant expansion project in Hillerød?
Product Specialist - Oral Solid Dosage Forms
Are you passionate about providing expert product knowledge and setting the direction for future tablet production to the benefit of our patients?
Supporter for Quality Control Laboratory
Do you want to be a part of the quality control of products in the Biotech and Rare Disease Quality Control (QC) portfolio?
Senior QA Professional
Are you an experienced Quality Assurance professional with a passion for ensuring high standards and compliance?
QC Equipment & IT Professional
Do you want to be part of ensuring fast delivery of quality products to our patients?
Associate Manager
Are you ready for an exciting job opportunity within an ambitious team where you will lead and set direction for highly skilled analytical scientists and technicians?
Global Regulatory CMC & Device Lead
We are rapidly expanding our product and project pipeline in Novo Nordisk and are looking for an experienced Global Regulatory CMC &...
Scientist - Mammalian Cell Cultivation
Do you have experience with mammalian cell cultivation at a pilot scale or motivated to learn?
Associate Manager for API Business Support
Do you thrive in a changing and fast paced environment where collaboration is the key to succeed?
Senior QA Professional for QC validation
Are you thrilled about working with modern technology and pushing the boundaries of process performance and production technology?
Quality Assurance Analyst - Pharmaceuticals and Hormonal Contraceptives, Supply Chain Management Unit (SCMU), Copenhagen
The Quality Assurance Analyst position is within the Product Quality Assurance Team in the UNFPA Supply Chain Management Unit (SCMU).
