QA Proces Supporter

Kunne du tænke dig at være en del af et mindre QA-team med store ambitioner?

ChemoMetec er en af verdens førende producenter af udstyr til celletælling og -analyse. Du kommer bl.a. til at supportere QA i den daglige drift (Customer Complaints, reparationssager, afvigelsesbehandling, ændringsansøgninger, kundekommunikation).

Du kommer også til at supportere QA i opbygningen af et nyt kvalitetssystem.

Clinical Operations Manager

Do you want key operational responsibility in phase 1-4 clinical trials as part of a high performing team?

As Clinical Operations Manager you are indispensable in the trial, leading and executing all the operational aspects throughout the different trial stages. You work closely with the Clinical Project Manager who is responsible for the clinical and strategic deliverables.

QA Device Senior Manager

Currently, we are looking for a new QA Device Senior Manager, who has experience with providing QA support to Drug/Combination Products development projects (early phase to Commercial).

You will be responsible for supporting our device development projects with setting direction for device quality in terms of internal and external requirements.

We bond as a result of our entrepreneurial culture where our people are encouraged to pursue their ideas and turn them into reality. We are curious about each other’s knowledge and expertise.

Specialist til API-produktion i København - Vær med, når vi redder liv

Du vil lede root cause-analyser, koordinere kvalitetsopgaver, være ansvarlig for kvalificeringer/valideringer af procesændringer, følge op på produktionsdata samt overvåge processerne. Arbejdet foregår i tæt samarbejde med kvalitetsafdelingen og den tekniske afdeling. Du vil ligeledes opleve operatører, teknikere, specialister og API-ledelsen som vigtige interessenter.

I stillingen vil dit primære ansvar og dine opgaver være:

• teknisk sparring og processupport til produktionen
• håndtering af kvalitetssager

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).

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.

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.

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.

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.

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.

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.

Manufacturing Supporter

We are looking for a talented Manufacturing Supporter for the Drug Substance Production to join the DS Documentation and Support Department in Hillerød.

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us.

You will be part of a team, consisting of 14 people, with a great sense of humor and a high willingness to support where needed.

Drug Substance CIP Process Supporter

Are you passionate about pharmaceutical CIP? Do you know processes and optimizing production?

As a CIP Process Supporter (Cleaning In Place), you will have a cross-functional role as a link between production, support teams, and technical support.

Your primary focus will involve optimizing our vaccine production and ensuring robust operation in line with CIP requirements and regulations. Additionally, you will play a vital role in daily troubleshooting, collaborating across diverse professional groups to ensure a streamlined production process.

Clinical Trial Manager til innovativt forskningsmiljø inden for hjertesygdomme og randomiserede studier

Er du en stærk analytiker med erfaring i at planlægge og udføre kliniske forsøg? Vil du være ansvarlig for at starte nye internationale kliniske forsøg op i Danmark sammen med vores samarbejdspartnere?

Kunne du tænke dig at arbejde med at gøre vores vision om kortere vej fra forskning til patientbehandling muligt?

Din opgave som Clinical Trial Manager vil være at lede implementering, udførelse og afslutning af kliniske forsøg i henhold til gældende studieprotokol og retningslinjer for Good Clinical Practice (GCP).

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.

Automationsingeniør med erfaring indenfor Pharma

Vil du arbejde med spændende og varierende projekter indenfor automation og kunne du tænke dig at blive del af et dygtigt tværfagligt team, hvor humøret og ambitionerne er tårnhøje?

Vi arbejder i Pharma automation teamet dedikeret med design, programudvikling, indkøring, test og kvalificering af procesløsninger til vores pharma og biotech kunder og du bliver således en del af vores tværfaglige projektteams.

På kontoret i Kalundborg vil du indgå i et professionelt fagmiljø, hvor der er fokus på vidensdeling og det gode samarbejde. Din dagligdag bliver præget af gode kollegaer, faglige udfordringer og stor medbestemmelse.

Manufacturing Associate - Operator

We are looking for process operators, preferably with experience from a similar pharmaceutical production company or similar regulated businesses OR a Life Sciences Graduate who have recently finalized their Bachelor or Master degree relevant for Biologics Manufacturing and are keen on starting their career in a manufacturing and international environment where things move fast.

We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools.