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Jobindex A/S
Scanpharm søger senior QA-Manager

Jobindex A/S søger for Scanpharm A/S i Birkerød

Vil du sætte dit præg på kvalitet og være med til at strukturere og videreudvikle kvalitetsafdelingen og fastlægge nye kvalitetsmål? Vi søger en erfaren QA-Manager til fastansættelse snarest muligt hos Scanpharm AS i Birkerød.

I jobbet som QA-Manager skal du lede personalet, fastlægge kvalitetskrav, forestå myndighedsinspektioner og kundeaudits, sikre målopfølgning, afholde QMR og have det overordnede kvalitetsansvar; dvs. sikre kvalitet og compliance ud fra de myndighedskrav, som vi efterlever. Du skal derfor være med til at sikre løsninger, som integrerer kvalitet og compliance i Scanpharm.

Jobindex A/S
Agilent Technologies Denmark
Clinical Research Associate with medical writing experience

Agilent Technologies Denmark, Glostrup

We are looking for a Clinical Research Associate to join our Global Clinical Affairs team in Agilent. In this role your primary responsibility is to compile clinical performance data for all Pathology CE marked products for reporting purposes in compliance with IVDR (EU) 2017/746. These activities will be conducted in close collaboration with Research & Development, Quality Assurance, Regulatory Affairs, and other internal stakeholders. Additional responsibilities will include the planning, coordinating and management of the day-to-day running of clinical studies to support regulatory applications and scientific marketing activities.

Responsibilities include the following:

  • Assist in developing Clinical Performance Plans for products planned for CE marking
  • Research internal controlled documents and IFU for existing clinical performance data
  • Conduct literature searches
Agilent Technologies Denmark
KLIFO A/SClinical Supply Coordinator for our Glostrup office

KLIFO A/S

As a Clinical Supply Coordinator you will support Clinical Supply Managers and be involved in supply activities, such as:

  • Prepare and approve label text according to Annex 13
  • Order packaging materials and labels
  • Prepare packaging records and other study specific documents
  • Control printed study specific labels
  • Coordinate return and destruction of IMP

An ideal candidate is a person committed to creating and delivering solutions that meet individual customer needs. Also, the person must have a positive, proactive and flexible personality.

LundbeckPrincipal Professional / Specialist, PV Quality Management System

Lundbeck, Copenhagen

Are you passionate about pharmacovigilance and making a difference for Patient Safety? Are you motivated by process mapping, writing and managing SOPs? Do you have profound ability to “connect the dots” and coordinate across? Are you an expert in pharmacovigilance processes with a strong drive to build innovative QMS documents? If yes, you may be just the person we are looking for.

You will be overall responsible for managing the PV QMS, including supporting the Line of Business and the GPS Leadership Team in ensuring that the QMS is complete and without gaps, and compliant with current global regulatory requirements. You will support GPS staff in the development and maintenance of steering documents to ensure lean, innovative user-friendly QMS documents. Further, you will have continuous oversight of the QMS and coordinate and manage periodic reviews, deviations and SOP training compliance.

LundbeckToxicologíst

Lundbeck, Copenhagen

Lundbeck is looking for a talented scientist with broad expertise in toxicology, chemistry and molecular biology to join the Department of Regulatory Toxicology & Safety Assessment.

You will be an important player in a department that participates in the full development process of pharmaceuticals from early research to post-marketing commitments. You will be the main person responsible for supporting our production units with non-clinical expert assessments of pharmaceutical and chemical entities and you will provide advice on how to use the assessments in practice across all development projects.

GEA Process Engineering A/S
Project Manager

GEA Process Engineering A/S, Søborg

GEA is looking for an experienced project manager for technical project execution. The position is placed in GEA’s Chemical divisions Pharma team located in Søborg.

Unik System Design A/S

As a project manager you will be responsible for one or more projects. Your responsibility will include all aspects of project execution from contract negotiations to the final takeover of the plant according to the GEA Project Management plan. You will facilitate the installation and take the lead in the commissioning of the plant.

Tasks will also include:

  • Acting as technical support during sales in close cooperation with the area sales managers
  • Generating a basic engineering package including technical specification of the plant, facilitating flow sheets and P&I diagrams
  • Facilitation of plant layout
GEA Process Engineering A/S
Lagkagehuset
Quality Manager

Lagkagehuset, København

Har du erfaring med kvalitetsarbejde, fødevaresikkerhed og arbejdsmiljø? Evner du samtidig at sætte rammer og retning, så dine kolleger tager procedurer, processer og arbejdsgange til sig i en omskiftelig hverdag?

Som Quality Manager får du en stor aktie i at sikre høje kvalitets- og hygiejnestandarder, branchens bedste fødevaresikkerhed og rammerne for et godt arbejdsmiljø på tværs af virksomheden. Med arbejdsopgaver over hele landet, har du et særligt fokus på at supportere vores butikker og produktionsafdelinger. Du bidrager samtidig tværgående og på gruppeniveau med såvel projekter som egne ansvarsområder.

Dine opgaver bliver blandt andet, at:

  • Opbygge og eksekvere stærke processer for hygiejne, rengøring, fødevaresikkerhed og arbejdsmiljø
  • Virke som tæt sparringspartner for salgs- og produktionsledelsen
  • Varetage myndighedskontakt og bygge bro mellem lovgivning og den daglige drift
Lagkagehuset
Miljø- og FødevareministerietKemikaliekontoret i Miljø- og Fødevareministeriets departement søger barselsvikar

Miljø- og Fødevareministeriet, København

Vil du gerne arbejde med at sikre et sundt miljø? Og synes du, det kunne være spændende at beskæftige dig med kemi i industri og forbrugerprodukter, regulering af kemikalier, herunder pesticider og biocider både i EU og internationalt? Så er du måske en af vores nye kollegaer i Miljø- og Fødevareministeriets departements Kemikaliekontor.

Du har en relevant profil fx. farmaceut, biolog, ingeniør, dyrlæge, magister eller lignende med naturvidenskabelig baggrund.

Du har lyst til både at bruge din naturvidenskabelige faglighed og flair for den politiske kontekst til blandt andet at udarbejde forelæggelser til minister, faglige notater og forberede og deltage i møder i Danmark og udlandet.

AGC Biologics A/S
Warehouse Technician

AGC Biologics A/S, Søborg

Do you want to join AGC Biologics on a journey to produce a product that hopefully can help the world out of its current health situation?

This is an excellent opportunity for someone truly interested in being a part of a strong and self-depended team, which in the near future will support manufacturing 7 days a week. You will be working different shifts and have at least one (1) Monthly work weekend. You will be able to participate in streamlining material handling and optimize activities in order to enhance compliance and minimize lead-time.

Responsibilities:

  • Being part of day2day Goods reception. Picking and Weigh and Dispense activities
  • Participate in emptying quarantine area, remove expired materials etc.
  • Participate in audit readiness, logbook review, monthly cleaning etc.
AGC Biologics A/S
AGC Biologics A/S
Qualification/Validation specialist for Quality Assurance Facilites & Equipment

AGC Biologics A/S, Søborg

The department is looking for a qualification/validation specialist and as a qualification/validation specialist, you will work with qualification of equipment, facility and utility in manufacturing and QC laboratory and also Cleaning Validation will be part of your work.

You must enjoy performing practical qualification work on the shopfloor but at the same time have a scientific approach in trouble shooting and qualification. You must be able to handle challenges in a busy environment with a positive mind set. The main responsibility of the QA Facilities & Equipment team is to ensure that our production facility and laboratories at all times are in accordance with current standards for GMP production, i.e. EU GMP, 21 CFR and ICH guidelines.

AGC Biologics A/S
LundbeckSenior Specialist for Upstream Process Development, CMC Biologics

Lundbeck, Copenhagen

We are looking to add a new Senior Specialist with strong experience within upstream process development and manufacturing to our CMC Biologics team. The team is responsible for the strategic- and technical leadership of pharmaceutical development activities in support of our biologics pipeline - spanning from pre-IND stage through process validation and launch.

As a Senior Specialist, you will join focus teams responsible for the development for our biopharmaceutical drug candidates and you will work closely with colleagues responsible for the development of drug substance, drug product, and analytical methods with the aim of achieving project objectives and global registrations for our biopharmaceutical drug candidates.

LundbeckProject Director for CMC Biologics

Lundbeck, Copenhagen

We are looking to add a new Project Director to our CMC Biologics team with strong experience within Project Management of biologics, coordination of cross-functional activities and handling of external collaborations. The department is responsible for the strategic- and technical leadership of pharmaceutical development activities in support of our growing biologics pipeline - spanning from pre-IND stage through process validation and commercialization.

As a Project Director, you will be leading project teams with representation of different areas of process development, manufacturing, regulatory affairs, clinical supply, CMC QA, Supply Chain and coordinate activities within development and manufacturing of our biopharmaceutical drug candidates including external collaborations at CMO and CRO’s.

LundbeckProcess Validation Senior Specialist for CMC Biologics

Lundbeck, Copenhagen

We are looking to add a new Senior Specialist with strong experience within Process Validation in manufacturing of biopharmaceuticals to our CMC Biologics team. The team is responsible for the strategic- and technical leadership of pharmaceutical development activities in support of our biologics pipeline - spanning from pre-IND stage through validation and launch.

As a Senior Specialist, you will join focus teams responsible for the development for our biopharmaceutical drug candidates and you will work closely with colleagues responsible for the development of drug substance, drug product and analytical methods with the aim of achieving project objectives and global registrations for our biopharmaceutical drug candidates.

LundbeckAnalytical Specialist for CMC Biologics

Lundbeck, Copenhagen

We are looking to add a new Specialist with strong experience within analytical development, release and characterization of biologics to our CMC Biologics team. The team is responsible for the strategic- and technical leadership of pharmaceutical development activities in support of our biologics pipeline - spanning from pre-IND stage through validation and launch.

As a Senior Specialist, you will join focus teams responsible for the development for our biopharmaceutical drug candidates and you will work closely with colleagues responsible for the development of drug substance, drug product and analytical methods with the aim of achieving project objectives and global registrations for our biopharmaceutical drug candidates.

Amgros I/SDynamisk teamleder til Amgros’ nye indkøbsteam i vores Logistikafdeling

Amgros I/S, København

Er du Amgros’ nye teamleder, der skal være med til at forankre og udvikle Amgros’ nye indkøbs- og lagerteam? Har du flere års erfaring med supply chain? Og er du en leder, der både forstår at prioritere, træffe beslutninger og samtidig formår at inddrage og udvikle dine medarbejdere, så læs endelig videre.

Stillingen som teamleder er en nyetableret stilling i logistikafdelingen, hvor du bliver leder for fire dygtige medarbejdere. Stillingen byder på opgaver af både strategisk og driftsmæssig karakter. Du forventes derfor at have en bred erfaring indenfor supply chain samt ikke mindst interesse og erfaring indenfor ledelse. Teamlederen refererer til afdelingschefen i Logistik.

AGC Biologics A/S
Operational Scientist for biopharmaceutical production – Downstream Team

AGC Biologics A/S, Søborg

Are you passionate about providing professional support in our downstream team so that advanced medicine can be manufactured for the patients? Join a dynamic and international company where everyone is responsible for delivering right on time as one team!

We are seeking a dedicated scientist with experience preferably within API production or other areas within the pharmaceutical industry. AGC Biologics is a Contract Manufacturing Organization (CDMO) with facilities in Denmark, Germany, Japan and USA and with customers from all over the world. We have more than 30 nationalities employed and the daily language is English.

AGC Biologics A/S
CUSTOMER SERVICE COORDINATOR – SWEDISH SPEAKING

STORBJERG Search & Selection Recruiting on behalf of Zimmer Biomet Denmark

Would you like to become part of a leading medical device company, then this is your chance! – Interesting and challenging position as Customer Service Coordinator in the Shared Service Center located in Albertslund – As part of the Customer Service Team covering the entire Nordic Region, you will be working with focus on the SE market. Experience from the Healthcare segments would be an advantage but not a must.

STORBJERG Search & Selection
AGC Biologics A/S
Process Engineer with a passion for automatisation

AGC Biologics A/S, Søborg

Do you have a passion for automation in biopharma manufacturing? Do you want to be part of a company helping customers bring new advanced biological products to market? And would you like to work at our multiproduct facility in Copenhagen? Then join a dynamic and international company where everyone is responsible for delivering right on time as one team!

Your responsibilities are furthermore:

  • Equipment/facility fit and gap assessments for new product introductions, identifying and leading equipment and system purchase, upgrade or rebuild projects
  • Build business cases for investment applications
  • Stay current on newest biologics manufacturing technologies
AGC Biologics A/S
Statens Serum InstitutMedarbejder til ordremodtagelse og GDP-relaterede opgaver

Statens Serum Institut, København

Lager- og Ordreafsnittet på Statens Serum Institut (SSI) søger medarbejder til ansættelse snarest muligt.

I Lager- og Ordreafsnittet varetager vi salg og pakning af vacciner - primært til de praktiserende læger samt salg og pakning af ikke-registrerede veterinære vacciner og veterinære autovacciner til dyrlæger og landmænd. Dertil varetager vi også salg af antistoffer.

Dine primære arbejdsopgaver bliver:

  • ordrehåndtering af vacciner m.m. pr. telefon og internet
  • håndtering af restordrer og reklamationer herunder afvigelsesbehandling
  • booking og håndtering af diverse forsendelser til ind- og udland
Amgros I/SLægemiddelspecialist med interesse for supply chain

Amgros I/S, København

Vil du være med til at sikre, at de offentlige danske sygehuse har den rette medicin, til rette tid og i rette kvalitet. Altid med patienterne for øje og altid via tæt dialog og samarbejde? Så er det måske dig vi søger. Amgros styrker netop nu sin Logistikafdeling, og vi leder derfor efter endnu en lægemiddelspecialist, som skal være med til at styrke vores Logistikafdeling på det famarceutiske område.

Som lægemiddelspecialist bliver din overordnede rolle at afklare og løse forsyningsproblemer for kritiske lægemidler. Du vil være en aktiv deltager i at udvikle processer og værktøjer, der bidrager til at øge forsyningssikkerheden og bliver dermed en vigtig brik i arbejdet med at sikre at livsvigtig medicin altid er til rådighed og dermed sikre den bedste behandling af patienterne.