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Tablettekniker til Glostrup Apotek Magistrel Produktion

Vi kan tilbyde en sjov, spændende og anderledes arbejdsplads. Har du lyst til hands-on produktion af en stor variation af tablet-produkter, har vi jobbet til dig.

Du kommer til at indgå i et team, hvor du primært skal være med til at forberede produktion, indstille tabletmaskiner og producere tabletter.

Stillingen er en fastansættelse med et timetal på 160 timer/måned.

Project Manager

Do you have experience in driving technical projects and want to be part of a company on an exciting growth track?

You will contribute to projects ranging from new equipment lines to the replacement of existing equipment and systems. As a Project Manager, you will lead projects or be responsible for and execute work packages or tracks, depending on project size.

Project Coordinator

Do you have experience managing projects anchored to a GMP facility? Are you eager to contribute to the development of a newly established project team in a production environment?

As a Project Coordinator, you will participate in the successful planning and completion of projects related to the Drug Substance Manufacturing Processes. You will coordinate and follow up on a number of tracks that links to various projects.

Maskinkonstruktør

Brænder du for at arbejde inden for konsulentbranchen med konstruktion af maskiner og anlæg samt bidrage til løbende udvikling og optimering af produkter til vores kunder?

Du tilbydes et udfordrende og spændende job med stor grad af selvstændighed i en virksomhed med højt til loftet og et godt arbejdsmiljø. Du vil få mulighed for at arbejde med forskellige arbejdsopgaver såsom design & udvikling af nye såvel som re-design af eksisterende produkter, projektledelse, samt teknisk dokumentation i et tæt samarbejde med vores kunder.

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

Clinical Supply IRT/RTSM Specialist

Come help us deliver high-quality clinical trial supply to trials all over the world

We are looking for an IRT/RTSM specialist to help us ensure timely setup of IRT/RTSM systems to support the delivery of trial supply for Ferring clinical programs globally.

In this role you are expected to not only collaborate closely with cross-functional teams but also contribute to a knowledge-sharing mindset and promote a collaborative and innovative work environment. You must have a flair for respectful communication with a range of stakeholders such as Clinical Operations, IT and Quality Assurance.

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.

Sundhedsvidenskabelige specialister til arbejdet med HTA-forordningen (genopslag)

Har du lyst til at være med til at sætte den danske retning for implementering af HTA-forordningen, så er det måske dig vi søger i Lægemiddelstyrelsen til to nyoprettede stillinger!

Din dagligdag i denne stilling vil være både dynamisk, udfordrende og præget af meningsfulde opgaver. Du får chancen for at sætte dit præg på både det danske og europæiske arbejde med HTA forordningen. Et arbejde, der kommer til at få stor betydning for de danske HTA-organisationer, virksomheder og patienter.

Vi mener, at der skal være en god balance mellem arbejde og fritid, derfor tilbyder vi en stilling på 37 timer med mulighed for at arbejde hjemmefra.

QA Specialist for Environmental Support

In this role, you will join Bavarian Nordic's QA Organization as a QA Specialist tasked with establishing strong relationships with stakeholders, effectively communicating GxP requirements, and handling crucial Quality Events in the Quality Management System (QMS).

This is in the context of environmental monitoring, aseptic performance, and sterile & low bioburden processes in Drug Substance and Drug Product Production. Additionally, you will contribute to the ongoing improvement of QA processes to elevate overall quality standards.

2 Regulatory and Marketing Compliance Managers

Har du interesse for og meget gerne erfaring med Regulatory Affairs – og helt optimalt med Marketing Compliance – og vil du gerne arbejde mere målrettet med Marketing Compliance?

Dine arbejdsopgaver bliver bl.a.:

• Compliance review af marketingaktiviteter og -materialer for den farmaceutiske industri og anmeldelser til Etisk Nævn for Lægemiddelindustrien
• Oversættelser af regulatoriske og medicinske dokumenter (dansk/engelsk)
• Andre regulatoriske opgaver svarende til opgaverne i et dansk datterselskab: gennemgang og opdatering af produktinformation, regulatorisk review af artwork m.v.

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.

Scientist for Biomarker Assays

Are you eager to use your scientific skills and expertise in preclinical research?

As our new scientist, your tasks will include:

• Coordination and support of biomarker experiments, including supervision of lab technicians.
• Perform data analysis, interpretation, review, and reporting of study results.
• Development of new biochemical- and immunoassays and troubleshooting of existing assays.

Application Technologist

Tetra Pak Filtration Solutions is searching for an Application Technologist in the field of membrane filtration of milk and whey products, with the focus on optimizing the environment footprint and applications.

As an Application Technologist, your responsibilities will be:

• Planning, execution and documentation of technology and application testing at customers site and in our development center.
• Data collection from full scale systems in operation, with focus on optimizing system performance and membrane selection.

We offer you an equal opportunity employment experience that values diversity and inclusion Market competitive compensation and benefits with flexible working arrangements.

Laborant til meget velfungerende peptidkemi laboratorie

Som laborant i vores peptid laboratorie er dit og kollegernes fokus at skabe grundlaget for udvikling af nye lægemidler. Du giver dit vigtige bidrag ved at bruge størstedelen af din tid med at arbejde hands-on i vores state-of-the-art laboratorie.

Du får et meget alsidigt job med ekstraordinært gode muligheder for at lære nyt og udvikle dig. Du kommer til at udføre alle typer af opgaver fra betjening af robotter og forskellige instrumenter til vedligehold og procesoptimering. Du kommer også til at arbejde med databehandling og dokumentation.

Project Manager

Som Project Manager på fabrikken i Hobro vil dit job være opdelt i en projektlederrolle, og en rolle der dækker daglige driftsopgaver.

Du både deltager i og leder selvstændigt større projekter relateret til fabrikkens anlæg og udstyr - fx lokaleombygning, installation af ventilationsanlæg, dokumentation etc. Du skal planlægge og udføre projekter fra start til slut, herunder sikre at tidsplaner og budgetter overholdes, være primær kontakt til myndigheder og eksterne samarbejdspartnere samt udføre, lede og koordinere arbejdet i projekt teamet, så projekterne kommer godt i mål.

Manufacturing Support Documentation Associate

Do you have a flair for compliance and can handle many stakeholders? Are you looking for a position where you can take on responsibility?

About the position:

• Create and maintain records and procedures by collecting information from stakeholders to supply manufacturing with compliant documents.
• Start-up events and support investigations by giving input as procedural SME.
• Support the change process by writing SME assessment to ensure procedural alignment. Perform timely closure of action items to ensure reliable execution of production.
• Continuously improve the department processes and support stakeholder improvement projects.

Quality & Compliance Manager

Are you passionate about quality and decency, and do you want to hold a key position in a growing sound international company focused on sustainability? Then you should read on.

You will be a part of the global supply chain organization in Middelfart and report to COO. The area of responsibility is material quality, compliance, and risk management, and you will be the driver of creating a culture of continual improvement by identifying opportunities for efficiency and innovation within the quality and compliance area with a focus on sustainability and the global ESG agenda.

Nyuddannet naturvidenskabelig akademiker og kommende forretningsleder

Vi søger nu talentet, der drømmer om en fremtidig stilling som forretningsleder, at bidrage når strategiske beslutninger skal træffes og være med til at sætte retningen for Eurofins Miljø Danmark.

Eurofins Miljø er Danmarks største miljølaboratorium. Vi arbejder med kemiske og mikrobiologiske undersøgelser af vand, jord og luft - samt tilhørende vejledning inden for miljøområdet. Du vil starte din rejse i Eurofins i vores Water Quality Monitoring (WQM) afdeling, hvor vi arbejder med overvågning af hele vandmiljøet.