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CIM A/S

QA Engineer – ensure the quality of our software solutions for pharmaceutical drugs and devices

Viby J or Hørsholm

Se video om CIM A/S som arbejdspladsDo you want to play a key role in delivering software systems that are compliant to the pharmaceutical industry?

As Quality Engineer, you will work together with the project manager, the software developers and the customers validation teams and help secure that our solutions are compliant and lives up to the customers expectation so they can re-use our validation as their own.

You are the expert on what makes you happy and efficient. So, whether that entails a 4-day work week or working in the evening or from home that is simply how you will be working.

CIM A/S
Fujifilm Diosynth Biotechnologies

Operators for Drug Product Manufacturing

Hillerød

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
Ferring Pharmaceuticals A/S

Clinical Supply IRT/RTSM Specialist

Kastrup

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.

Ferring Pharmaceuticals A/S
Ferrosan Medical Devices A/S

Senior Process Specialist

Søborg

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.

Bavarian Nordic A/S

QA Ext. Manufacturing Specialist

Kvistgård

Se video om Bavarian Nordic A/S som arbejdspladsWould you like to work in one of the most interesting, complex, and dynamic areas in Bavarian Nordic? Are you ready to engage, support, and mobilize colleagues in a growing international business environment where we focus on saving lives every day?

As a QA Specialist, you will be responsible for daily support, QA oversight, and GMP guidance to Contract Manufacturing Organizations (CMOs) to ensure that our products are manufactured according to current GMP and our marketing authorizations.

Bavarian Nordic A/S
Unilever Danmark A/S

Process and Innovation Lead

Odense C

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.

Green Hydrogen Systems A/S

Process Engineer

Kolding or Copenhagen

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.

Green Hydrogen Systems A/S
Ferrosan Medical Devices A/S

Senior QA Specialist

Søborg

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.

PRO&CO søger for Everfuel A/S
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PRO&CO

Automation Engineer

Fredericia

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.

PRO&CO
Gem
Convatec

Test & Reliability Engineer - Sustaining Engineering, Medical Devices

Lejre

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.

Convatec
Fujifilm Diosynth Biotechnologies

Manufacturing Associate - Operator

Hillerød

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.

Gem
EPOS

Data-Driven Production Test Engineer with Coordination Skills

Ballerup

Do you have experience with data management, production data analysis and databases?

You will administer the operation of the WATS database (our main production database) and auxiliary data systems for test reporting. You will be constantly in contact with the team and suppliers to identify data chain gaps & potential improvements. Correspondingly, you are able to map WATS features to our organizational needs and potential improvements.

EPOS
Pharmacosmos A/S

QA Specialist

Holbæk

We are seeking a competent new colleague to join our QA team in a dynamic and growing company.

You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.

Pharmacosmos A/S
Gem
Convatec

Validation Engineer

Lejre

As our new Validation Engineer, you will be responsible for validation and qualification of processes and equipment related to customer projects.

Key responsibilities in this role include, but are not limited to:

  • Validation and Qualification of processes and equipment when implementing new material.
  • Perform Validation and ensure results are accurately documented.
Convatec
QV-Compliance A/S

Ingeniør til validering

Roskilde

Vi har brug for en konsulent til et spændende job indenfor kvalificering og validering. Stillingen byder på mange forskellige opgaver og projekter hos vores kunder på det meste af Sjælland, og du får en spændende, travl og varierende hverdag.

Du vil bl.a. koordinere, planlægge og udføre validerings- og kvalificeringsprojekter, som kan omhandle: rengøringsvalidering, sterilisationsprocesser, procesanlæg, IT-validering, klimafaciliteter, produktions-, måle- og laboratorieudstyr.

QV-Compliance A/S
HydraSpecma A/S

Research & Development (R&D) Manager

Skjern and Silkeborg

As our R&D Manager, you will:

  • Play a pivotal role in our Technology organization.
  • Be part of a collaborative and professional R&D team, driving innovation and improvements at every level.
  • Good opportunities for personal and professional development in an international corporate environment.

Embrace this opportunity to become a key player in an international company where your skills in leadership, creativity, and innovation can flourish.

Process Supporter

Hillerød

Would you like to work with the latest processes and technologies in pharma?

Global Process SME and Product Owner

Ballerup

Are you passionate about process optimization and finding best solutions?

Indrykket:

Senior Equipment Specialist for API

Hillerød

Are you energised by using this knowledge to guide and mentor others to succeed?

Manager for Assembly Process

Hillerød

Do you have a background in the pharmaceutical industry and possess leadership skills?

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