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32 jobannoncer matcher din søgning 32 jobannoncer fundet
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QA Manager
Your success will depend on your ability to excel as an inspiring, supportive, and motivating leader, while effectively managing stakeholders in a complex and dynamic organization.
You will
- Provide leadership and inspire continuous development of the team members through coaching and dialogue.
- Lead the quality team and ensure high motivation and work-life balance.
Analyst and Project Coordination In Life Science Consultancy
Would you like to work with data analysis and research of worldwide trends in the pharmaceutical and biotechnological industries?
You will get the responsibility of managing and coordinating the day-to-day operations needed to solve our projects and writing reports for our commercial unit.
An academic background in life science (pharmacy, biotechnology etc.), economics or similar is required.
Supporter til produktionsforbedringer og drift
Vil du være med til at bekæmpe kræft?
Brænder du for at lave forbedringer af processer og produktionsfaciliteter, samtidig med, at produktionen holdes kørende?
Dine opgaver vil være at stå for store og små procesforbedringer. Det kan være mindre tilretninger af SOP’er eller store forandringer som fundamentalt ændrer vores måde at arbejde på.
Vi tilbyder masser af ansvar og indflydelse på dine arbejdsopgaver.
Akademiker til daglig support og procesforbedringer
Vil du være med til at bekæmpe kræft? Brænder du for at lave forbedringer der sikrer høj kvalitet? Er du klar til at gøre en forskel for dine kolleger og forbedre produktionsfaciliteterne til gavn for Agilents kunder?
Dit hovedansvar vil være at sikre GMP-niveauet i produktionen. Du vil i den forbindelse skulle afklare GMP-spørgsmål samt udarbejde Non-Conformance Reports (NCRs).
Global Regulatory Specialist, Plant Health (temporary position)
As Regulatory Affairs Specialist you will be part of the Global Regulatory Affairs team, with around 18 team members across the globe. You will work closely with stakeholders in the Plant Health industry and support the execution on regulatory strategies globally.
You will interact with cross-functional product and project groups and maintain close interaction with stakeholders in biotechnology, other parts of R&D, sales, marketing and with strategic customers and authorities.
Formulation Scientist
Are you looking to use and grow your experience in formulation development in a broad role with independent responsibilities? Do you want to drive formulation projects and contribute to the strategic development of future products?
In this role, your overall focus will be formulation development of drug products. Your responsibilities will cover formulations used for toxicology and clinical studies through the development phases and all the way to the commercial drug product.
Experienced Scientist for validating QC methods in Novonesis
Do you want to work in an environment where great collaboration is valued as highly as scientific excellence?
Working as Scientist in our team, you will be responsible for validating and optimizing analytical methods for Human Health products in our QC labs. You will work closely with other scientists and laboratory technicians to plan and implement efficient microbiological methods.
Operators for Drug Product Manufacturing
Would you like to be part of an international pharmaceutical company in rapid growth, which offers good development opportunities and set shifts?
This project is in the early phase of establishment and in the beginning, you will help design and establish processes for the upcoming production.
Main tasks:
- Participate in running and validation of equipment on site
- Assist during installation of equipment on site and carry out qualification tests afterwards
Operations Data Coordinator for Drug Substance Production
The primary task within the position is to collaborate with various departments (e.g., automation, tech transfer, and manufacturing departments) to collect and translate information required for building efficient production campaigns and daily task schedules.
You will be part of a team with a great sense of humor and a high willingness to support where needed.
Lab Quality Coordinator, GCLP Laboratory
As Documentation Coordinator at the laboratory in Lund at MinervaX, you will play a central role in the establishment of a GCLP laboratory for clinical samples from MinervaX’s prophylactic vaccine targeting Group B Streptococcus (GBS). The GLCP laboratory is established to move into phase III clinical trials. You will be responsible for the writing, coordination, storage, and maintenance of documentation in the whole laboratory area.
This is a unique opportunity to join the journey into building a GLCP compliant laboratory. As this is a new position you can develop this role according to your own ambitions and will be primary person on documentation support.
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.
Senior Life Science Business Consultant
Are you an experienced Senior Life Science Business Consultant with a passion for combining life sciences with the business aspects of consulting?
Don't miss this opportunity to advance your career and collaborate with our skilled colleagues to transform the digital landscape for clients all over the world.
You will plan and execute projects for our clients – working collaboratively with others. You will be deeply involved in all project phases from the idea phase, to identifying the value adding areas, analyzing current and future processes and technology needs, vendor selection and implementation.
Senior Research Technician
Do you want to use your experience and problem-solving skills to work with pharmaceutical product development and early-stage development with a focus on characterization (MFI, DSC, HPLC)?
As a senior research technician, you will spend most of your time in the lab, where your primary role will be to prepare, plan, and perform pharmaceutical development work, including stability studies.
Clinical Project Manager
Do you want impact, freedom to perform, global perspective and super colleagues?
As experienced Clinical Project Manager, you naturally know that your success is built on your ability to generate high quality data at high pace and within agreed budgets – without jeopardizing the good relationship to the people and partners involved. Another vital part of your road to success is your ability to think outside the box and handle (unforeseen) challenges on the way.
Research Analyst
Are you in the right job? Do you want a challenge out of the ordinary?
The Primary Research Analyst has the responsibility of identifying, developing, and maintaining a network of contacts and relationships in the pharmaceutical and biotech industry and organizations.
An academic background in pharmacy or in biotechnology is an advantage but not a necessity as extensive internal training will be provided.
SAP Master Data Specialist
Do you want to be a part of Process Support in a company with a unique impact on global healthcare?
You will be coordinating SAP production master data activities throughout the organization in order to achieve safe and predictable product implementation, maintenance, and decommissioning.
Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.
Technician, EMA Solids Support Team
Welcome to Solid Support Team 13 skilled process engineers and technicians responsible for quality, introducing new products, throughput, and optimizing the products.
In this role you’ll make an impact by:
- Responsible technician for the MG-coating line, ensuring smooth and efficient coating processes for granulating with MnTACN
- Coordinate the steering system changes, bridging the gap between process engineers, technicians, and programmers to optimize operational efficiency.
Regulatory Affairs Manager
The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.
This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:
- Ensure regulatory compliance to maintain market approvals
- Lead a team of skilled RA associates
- Ensure alignment with relevant stakeholders
Advanced QA Professional
Are you ready to play a crucial role in ensuring the quality and safety of our products for patients worldwide?
Medical Doctor within Pharmacovigilance
Are you eager to leverage your skills and experience in pharmacovigilance to play a key role in ensuring the utmost safety...