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73 jobannoncer matcher din søgning 73 jobannoncer fundet
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Clinical Trial Assistant
Are you looking for the possibility to unfold your competences within clinical operations even further? Do you thrive in an innovative environment working alongside dedicated clinical research professionals? Are you a self-driven team player, who enjoys a varied and influential day at work?
Pharmacosmos A/S is a progressive and innovative pharmaceutical company with headquarters in Holbæk, Denmark. We are on an exciting journey of global growth inventing new and innovative treatments, and right now we are expanding our team with a Clinical Trial Assistant.
Senior Vice President, Global Chief Medical Office
We are seeking a highly experienced and dynamic medical executive to join our Global Research & Development organisation in a newly established senior leadership role as SVP, Global Chief Medical Office (GCMO).
In this role, you will act as scientific advisor to the EVP of R&D and the Global R&D leadership team, and your primary objective will be to ensure “one global medical voice” for ALK internally and represent the medical voice of ALK externally.
Manager Virus Production
Do you want to play a central and important role in Bavarian Nordic´s manufacturing strategy by setting directions and ensuring smooth daily operation in our production facility?
Our newly established Drug Substance Facility in Kvistgaard will soon start production ramp-up, and we therefore need to strengthen our leadership. You will become responsible for the day-to-day shopfloor management of 15-20 operators.
Specialist, Regulatory Affairs (Temporary Position)
As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.
Further, your main responsibilities include to:
- Gather information and documentation for variation applications
- Update dossier sections
QA Specialist
We are seeking a competent new colleague to join our QA team in a dynamic and growing company.
You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.
Creative Assistant
Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?
Your Focus will be:
- Always following correct compounding procedures
- Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
- Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.
Associate Sensory scientist/Sensory Panel Lead - Arla Innovation Centre, Aarhus
We are looking for two new Sensory Panel Leads. One new collegue for a 1 year maternity cover and one for a 3 year project. For both positions we hope we will be able to prolong the employment or offer new challenges within Arla Foods.
Your key responsibilities will be:
- In close contact with stakeholders, guide and choose the proper test-setup to deliver the sensory results needed
- Panel training and development of panel competences within specific areas of interest
Technical Specialist, Product Quality, Nourish (Maternity cover, 12 months)
Are you an enthusiastic, motivated and detail-oriented professional with a desire to work in a team of colleagues with great technical competencies within production, regulation and processes?
Your core responsibilities:
- Handling deviations for products manufactured at our factories.
- Handling of product quality related complaints.
- Coordinate and implement customer-specific requirements. Maintenance of master data in various IT systems, including SAP.
Health, Safety and Environment (HSE) Manager
Are you a seasoned Health & Safety professional seeking an opportunity to thrive in a supportive and dynamic environment?
We have an exciting opportunity to recruit a Health & Safety Manager, you will play a crucial role in maintaining and enhancing the safety standards at our facility. Your responsibilities will include designing training programs, conducting risk assessments, identifying, and controlling hazards.
Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)
At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.
The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.
You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.
Department Manager for Molecular Pharmacology
Gubra is seeking a dedicated and experienced Department Manager to lead our Molecular Pharmacology department. The ideal candidate will possess proven leadership abilities and a passion for managing and developing teams, along with a background in molecular pharmacology and drug discovery.
Your tasks include
- Daily management of a team of scientists and lab technicians to ensure high performance, personal development, well-being and engagement.
- Guide the team to accomplish department goals and objectives.
- Oversee the planning, execution, and analysis of experiments to support Gubra’s internal and partnered drug discovery projects.
Fødevarefaglig Quality Manager & Labeling Specialist
Interesserer du dig for det tekniske område inden for fødevarer, og trives du i specialistrollen, hvor du sidder med ansvar for områder som mærkning af fødevarer, egenkontrolprocedurer, kvalitetskontrol, importforordninger, fødevarelovgivning, m.m.?
Som Labeling Specialist & Quality Manager hos Janax vil du blive budt på en spændende og afvekslende hverdag. Det er vigtigt, at du motiveres af hele processen fra at dykke ned i lovgivning til at analysere, planlægge, koordinere og kommunikere, mens du holder det forkromede overblik.
Senior Engineer Device Manufacturing
Are you passionate about cutting-edge medical technology? Do you thrive in a collaborative environment where innovation drives patient care?
Amgen, a global biotechnology leader, is expanding its device development capabilities in Denmark and is seeking a talented Senior Engineer to join our Device Engineering group.
Laborant eller procesoperatør til bufferproduktion til cancerdiagnostik
Vil du bidrage til diagnostik af cancer og gøre en forskel for patienter? Bliver du motiveret af laboratoriearbejde i et travlt produktionsmiljø? Er du detaljeorienteret og lægger vægt på korrekt produktion og dokumentation?
Vores hverdag består hovedsagelig af produktioner, grundig dokumentation og reviews men vi prioriterer også tid til løbende forbedringer af vores arbejdsgange og processer.
Der er tale om en fuldtidsstilling på 37 timer per uge. Arbejdstiden ligger i dagtimerne og vi har flextid.
Senior Process Specialist
Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.
You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.
Process Specialist
Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.
Together with the rest of the team, you will be responsible for the daily support of our production lines. You will learn our processes in detail and gain a good overview of the documentation used in production.
Kickstart your career as a Life Science Business Consultant
Looking for the opportunity to combine your interest in life sciences with the business aspects of consulting?
Then grab this career-building chance to work with and learn from talented colleagues as you help digitalize the clinical landscape for clients across the globe.
Not only will you get to hone the skills that will make you a good consultant, but you’ll also get to see the direct impact of your work as you help pharma companies make a difference in patients’ lives
Continuous Improvement Partner
As a Continuous Improvement Partner in Drug Substance Manufacturing, you will be part of a team of Improvement Partners who develops and sustains systems and tools that enables the organization to consistently increase the level of operational excellence in manufacturing.
Your primary tasks will include but not be limited to:
- Develop and sustain CI systems and tools.
- Coach on ideal behaviour that drives a proactive improvement culture.
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.
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.