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Nyuddannet proces, - eller industrioperatør til fermentering i medicinalproduktion hos Xellia

Er du teamplayer af natur og parat til nye udfordringer?

Som operatør vil dine primære arbejds- og ansvarsområder være:

• fyldning, sterilisering, podning, fermentering og høst
• overvågning og betjening af procesanlæg
• overvågning og betjening af forsyningsanlæg, herunder vandanlæg og nedbrydningsanlæg

QA Assistant, GS-5, QAC

This position is embedded in the Quality Assurance Centre (QAC), where teams have coreresponsibilities around quality assurance and quality control of supply processes and the productswe procure and deliver.

The incumbent will beresponsible for assisting the Quality Assurance Specialist (non-pharma) in the management of all aspects of Pre-Delivery Inspection (PDI) arrangements for non-pharma items from initial request tofinal invoice certification.

Project Engineer – pharma automationsprojekter

Har du pharma-erfaring, og vil du være med til at tage en førende, international teknologivirksomhed til næste niveau på pharma-området, så er det nu, du har chancen. Om du vil have base i Ballerup, Kalundborg eller Middelfart er helt op til dig selv, så længe du er klar på at være minimum en dag om ugen hos kunden i Bagsværd og/eller Kalundborg – og dagligt i perioder med testaktiviteter.

Du bliver del af et internationalt projektteam sammen med 3-5 andre Application / Project Engineers samt en Lead Engineer. Du bruger og deler din gode viden og er med til at skabe den klassiske ABB-ånd kendetegnet ved hjælpsomhed, videndeling og plads til at have det sjovt sammen.

Warehouse Team Leader - Vejle Export Terminal

Are your passionate about inspiring, motivation, and coaching your team to work happily and deliver their best? Do you thrive in a busy operational environment, juggling multiple task, and are you interested in leading a dedicated team?

In close collaboration with the Warehouse Manager, you will lead a team of 22 skilled employees directly under your supervision. You are expected to develop employees’ skills so that we always have the right resource available to meet present and future demands.

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.

Mekanisk vedligeholder til produktionsanlæg og utility

BASF A/S Ballerup har gennem årene ved konstant innovation udviklet en proces, som er helt unik. Vi er specialiserede i mikroindkapslede formuleringer af vitaminer, carotenoider, fiskeolier og farvestoffer. Vi beskæftiger ca. 135 medarbejdere i Ballerup og søger nu en reparatør til vores Vedligeholds afdeling.

Som reparatør bliver du en afgørende brik i at opretholde vores produktionsudstyr og Utility på højeste niveau. Du vil arbejde tæt sammen med vores dygtige kollegaer og være bindeleddet mellem forskellige afdelinger. Hos os bestræber vi os på at skabe de bedste rammer for oplæring og muligheden for at du kan planlægge egen dagligdag og prioritere dine opgaver.

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.

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.

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.

Manufacturing Lean Leader

This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

As our new Lean Leader, you will lead the site’s Kaizen funnel, daily management system, coach colleagues and work on improving for a better tomorrow. You will lead and manage projects that positively impact operations.

You will be a key staff member of the site operations team, this role exercises a high level of operational judgment, and sets team priorities in alignment with the strategic imperatives of the manufacturing site.

Process and Innovation Lead

We are hiring a Process and Innovation Lead for our factory in Odense, where we produce detergents under our strong Home Care brands such as Neutral, Biotex, and OMO.

In this position you will be the owner of our fabric wash manufacturing processes in the factory. A critical part of this role will be ensuring an effective link with R&D, planning, and factory for innovation, capacity, and project delivery. You will be responsible for mapping potential sustainability projects.

Category Manager

Do you want to be responsible for developing our Sourcing of Packaging and Raw materials to new heights? Do you want to make a difference for patients undergoing surgery by securing the compliance of the medical devices used by healthcare professionals?

We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun.

Process Engineer

Are you an experienced process engineer with solid experience from process engineering, technology, or a production company? Do you have technical knowledge within thermodynamics, fluid dynamics, compressible flow, and process design?

Do you want to join us in accelerating the global energy transition? Then you might be the Process Engineer we are looking for to join our team at Green Hydrogen Systems.

Senior QA Specialist

You will be part of our QA Business Support Team, consisting of 12 QA Specialists and Senior QA Specialists, allocated to projects including innovation projects, capacity projects and strategic QA/QC projects. We participate in projects both as quality and compliance experts to ensure compliance with the requirements for Class III Medical Devices.

We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.

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.

Automation Engineer

Do you want to use your technical knowledge to work with complex systems related to hydrogen production plants (water electrolysis)? Do you have the motivation and ambition to make the world a better place to live?

You have technical knowledge and thrive working with complex systems As Automation Engineer at Everfuel you will be responsible for developing the automation architecture, specifications, designs, tools, and processes. You should expect focus to be on control loop optimization, functional safety, specifications design, and validation processes.

Project Manager – projects with direct customer dialogue

Do you first and foremost see project management as your profession?

Are you at the same time looking for an opportunity to utilize your experience to impact the overall direction for the future while at the same time working hands-on with exciting customers and projects? If so, this job is tailored to you.

Your focus will be projects centered on electrification/automation/control systems across Danish industry, energy and utility companies.

Vessel Manager - Offshore Wind Industry

Are you passionate about vessel operations and being the link between our colleagues on- & offshore? Then we can offer you this exciting role within the renewable business area.

You will be responsible for overseeing the safe and efficient execution of daily operations and maintenance scopes in close collaboration with vessel management team and shoreside departments.

We are looking for a people leader, who displays strong interpersonal skills and who has the ability to communicate effectively with a variety of stakeholders.

Test & Reliability Engineer - Sustaining Engineering, Medical Devices

Do you have a keen eye for Physical Testing, Product Quality, Reliability, Validation, and Documentation? Are you looking for an opportunity to merge your passion with our expertise in the Test and Verification of Infusion Care Medical Devices, for the treatment of chronic diseases such as Diabetes and Parkinson’s Disease?

As a Test Engineer, you will be involved in developing and working with a diversity of physical test methods. Planning and coordinating tests in our laboratory in Osted near Roskilde, and partners within Global Convatec and external. Most of your time, you will be part of a project team in SEG.