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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.

(Senior) Drug Substance Specialist

We are currently seeking a (Senior) Drug Substance Specialist who is energized by collaborative and fun teamwork, excels in handling complex tasks, and enjoys continuous learning.

Your responsibilities will include late-stage drug substance development, up-scaling and process validation as well as support in the commercial phase. Effective coordination with external partners is a significant aspect of this role.

Kemiker til QC med GMP-erfaring

Syntese A/S søger en erfaren kemiker med kompetencer og interesse for analytisk kemi og GMP. Stillingen er en udvidelse af nuværende team.

Dine primære opgaver er at indgå i afdelingens daglige drift, hvor du supporterer og godkender analyser i et tæt samarbejde med dine kollegaer i teamet. Du udarbejder afvigelser, opdaterer SOP´er og vedligeholder kvalitetssystemerne.

Junior Controller

Er du detaljeorienteret, selvkørende og forstår regnskabets mange facetter? Så er du den vi leder efter. I Steelcos økonomiafdeling har de brug for en dygtig, engageret og positiv junior controller.

Du vil fungere som højre hånd til Nordic Finance Director og vil skulle supportere med controlling, rapporteringer og statistikker.Derudover vil en del af dine daglige opgaver blive:

• Daglig bogholderi, herunder kontering og bogføring
• Betaling af kreditorer
• Rykning af debitorer

Senior LIMS Specialist for Global QC Development

In this role you’ll make an impact by working as a Senior LIMS Specialist in our team, where you will take part in management of projects for LIMS changes across QC laboratories and other stakeholders including implementation, documentation and communication.

Future projects could be introducing and validating LIMS solutions on new equipment or technologies, new LIMS functionalities, improving and aligning existing processes.

QA-specialist, der er QP-delegeret eller drømmer om at blive det

Drømmer du om at bidrage til at sikre kvaliteten af livsvigtige lægemidler, der redder liv? Er du en erfaren kvalitetsspecialist med erfaring fra lægemiddelproduktion?

Som delegeret Qualified Person (QPd) i vores Manufacturing QA (MQA) afdeling får du en unik mulighed for at arbejde med kvalitetssikring og frigivelse af Xellias produkter. Du vil være med til at sikre, at vores antibiotika når frem til patienter i hele verden i den højeste kvalitet. Som delegeret QP hos Xellia får du et stort ansvar.

Regulatory Affairs Clinical Specialist

Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.

Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.

Learning and Development Partner

Admitted, the headline in question is a song lyric by musician Beth Hart. Even though we aren’t looking for a singer-songwriter, we are on the lookout for someone who is just as motivated about inspiring growth and development as we are.

At Abacus Medicine we know how to live – but we would like to know more about how to learn, which is why we are looking for a Learning and Development Partner to help us in these efforts. In this position you’ll be given the opportunity to co-create and set the path for Abacus Medicine Groups future learning and developmental environment together with our Head of Group Learning and Development.

Elektriker til vedligeholdelsesarbejde i farmaceutisk virksomhed

Er du uddannet elektriker, og kunne du tænke dig at blive del af vedligeholdelsesafdelingen på en API site i rivende udvikling?

Og sætter du faglig stolthed i højsæde?

Så bliv del af et alsidigt håndværkerteam og få

• En spændende og udfordrende hverdag
• Frihed under ansvar
• Konkurrencedygtig løn

Account Manager – Pharma

Vi er inde i en kraftig vækst og positiv udvikling, og har derfor brug for en stærk Account Manager i vores salgsteam, hvor du får ansvaret for salget af vores løsninger til eksisterende og nye kunder indenfor medicinalindustrien.

Vi har en flad struktur med hurtige beslutningsprocesser, og vi vægter et godt teamwork, hvor der er plads til både det professionelle og det sociale. Du kommer til at være med til at præge udviklingen og retningen i vores salgsteam.

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.

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

Procurement Assistant

The Medicines and Nutrition Center (MNC) is part of Supply Division and manages the procurement and contracting of pharmaceuticals, and nutrition products for all UNICEF offices, Copenhagen warehouse and regional hubs, focusing on optimizing emergency response and access to affordable and quality assured products in a timely manner.

The Procurement Assistant will support the procurement cycle for a segment of Nutrition products and services. Providing effective services to customers, ensuring accurate and timely processing of requisitions and requests up to the completion and closure of the order, with the overall goal of meeting the needs and requirements of the customers.

Senior Specialist til QC hos Xellia Pharmaceuticals

Drømmer du om mere ansvar, med forskelligartede opgaver, og har du en passion for mikrobiologi? Vil du spille en central rolle i Xellias produktionen af livsvigtig antibiotika?

Som senior specialist vil du blive faglig ansvarlig for vores count release-laboratorie, som bl.a. udfører TVC- og LAL-analyser. Derudover vil du indgå i tæt samarbejde med vores sterile produktioner angående EM, hvor de nye Annex 1-krav stiller øgede krav til vores compliance, som du vil spille en vigtig rolle i.

Talent 2024: Start your career within Pharma & Life Sciences in CGI's MES/Automation talent program

Our most important task is to prepare you for the tasks you will solve. In cooperation with the companies that developed the systems, you will be certified in the technologies used, such as PROCOS, PAS-X and 800xA.

You will be involved in all phases of our projects, including sales support, consultancy, specification, design, engineering, construction, programming and testing, verification and validation, and commissioning with the end customer.

Senior Medical Writer

Do you want to work in a global context and according to the highest standards of current practice to provide new products to patients with unmet medical needs?

As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.

Topsoe Operations, Technical Service Team, Service Engineer

Your primary duties will encompass routine/scheduled and unscheduled maintenance and repairs, intended at preserving our equipment and machinery in their best condition, to deliver performance guarantees and turnkey solutions with end-to-end support and onsite availability to our customers.

You will play a pivotal role in guaranteeing the optimal operation and peak performance of our equipment and technologies installed at the customer Plant facilities globally.

Student Assistants for NBCD A/S within Clinical Operations

Do you dream of working with pharma and research? Are you curious, service-minded, and envision yourself thriving in a dynamic research environment with varied tasks?

Then come join us as a student assistant and become part of a company, that operate at the forefront of international drug development research, where you'll have the opportunity to broaden your skillset, shape your own day and contribute to various projects.

Regulatory Affairs Specialist

The RA Specialist for Radiometer is responsible for ensuring coordination of regulatory activities for a few of our Blood Gas products manufactured in California to help ensure continued compliance in all markets.

In this role, you will have the opportunity to:

• Facilitate coordination of regulatory activities between California and Denmark for design control activities and international registrations for a few of the instruments/consumables manufactured in our California site.
• Ensure compliance with EU regulations.
• Generate STED files, international submissions & assess design changes.
• Plan and execute projects for new regulatory requirements.

Senior Regulatory Specialist

The Senior Regulatory Affairs Specialist at Radiometer is responsible for collecting and generating documentation for product submissions to ensure compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world.

If you thrive in a fast-paced environment, are used to playing a critical supporting role and want to work in a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.