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Training Partner

Are you passionate about designing high impact training to improve ways of working?

The role will focus on re-designing the training related to onboarding our professionals working directly with our operation, our Operators, and our Laboratory Technicians.

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.

Lab Technician

Med laboratorier i USA, Storbritannien, Tyskland og Danmark har LGC Biosearch Technologies planer om at fortsætte med at vokse.

Vi søger i øjeblikket talentfulde kandidater, der er klar til udfordringen med at arbejde i en formålsdrevet organisation med høj vækst.

Du vil blive en del af et mindre team og indgå i produktionen, hvor der syntetiseres, oprenses, analyseres, kvantificeres samt laves QC kontrol af syntetiserede produkter.

Vi tilbyder en arbejdsplads med gode kolleger, højt humør, en attraktiv frokostordning og muligheden for massage, hvis ønsket er der.

Regulatory Affairs Specialist

The RA Specialist for Radiometer is responsible for ensuring coordination of regulatory activities for a few of our Blood Gas products manufactured in California to help ensure continued compliance in all markets.

In this role, you will have the opportunity to:

• Facilitate coordination of regulatory activities between California and Denmark for design control activities and international registrations for a few of the instruments/consumables manufactured in our California site.
• Ensure compliance with EU regulations.
• Generate STED files, international submissions & assess design changes.
• Plan and execute projects for new regulatory requirements.

Senior Regulatory Specialist

The Senior Regulatory Affairs Specialist at Radiometer is responsible for collecting and generating documentation for product submissions to ensure compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world.

If you thrive in a fast-paced environment, are used to playing a critical supporting role and want to work in a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.

Lab Technician – tidsbegrænset kontrakt

Vi søger hurtigst muligt en uddannet laborant – gerne nyuddannet – til vores laboratorium i Lystrup tæt ved Aarhus.

Du vil blive en del af et mindre team og indgå i produktionen, hvor der syntetiseres, oprenses, analyseres, kvantificeres samt laves QC-kontrol af syntetiserede produkter.

Vi tilbyder en arbejdsplads med gode kolleger, højt humør, en attraktiv frokostordning og muligheden for massage, hvis ønsket er der.

QC Laboratorie Supporter (Barselsvikariat 12 måneder)

Vi søger en person med det rette servicegen og energi, og som forstår kravene i et cGMP QC-laboratorium. Som vores kommende kollega er det vigtigt at du har forståelse for arbejdet i et laboratorie, er indforstået på en travl hverdag med skiftende prioriteringer.

Er det lige dig vi står og mangler, så kan vi tilbyde dig et spændende og udfordrende job i en virksomhed der går en spændende fremtid i møde med mange nye kunder og produkter og store muligheder for personlig udvikling og ansvar. Dette er en tidsbegrænset stilling, men vi udvider og vækster hele tiden så hvem ved hvad fremtiden bringer?

Fleksibel og nysgerrig QA-koordinator med lederpotentiale

Kan du se dig selv stå i spidsen for at sikre høj kvalitet for mere end 1500 forskellige produkter årligt?

For Persano Group søger vi en QA-medarbejder, som kan se sig selv vokse ind i en ledende funktion, og som har den rette mængde af drive, nysgerrighed og ejerskab til at bidrage i en familiedrevet virksomhed, hvor stor passion er den kultur, der gennemsyrer virksomheden.

Senior Test Engineer

Join GE HealthCare to help perform transducer integration on our next-generation ultrasound scanners and further develop our test tools and laboratories.

As our new Senior Test Engineer, your typical tasks will include measurements of sound pressure, acoustic power, thermal characteristics, image performance and other transducer properties.

You will take part in hands-on work while also playing a key role in maintaining and further developing our transducer integration processes and two laboratories.

Regulatory Affairs Manager

The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.

This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:

• Ensure regulatory compliance to maintain market approvals
• Lead a team of skilled RA associates
• Ensure alignment with relevant stakeholders

QA Specialist og Senior QA Specialist

For dig, der trives med at arbejde med kvalitet og lovgivning fra et operationelt perspektiv, både selvstændigt og i dialog med vores leverandører og interne afdelinger.

Som QA Specialist vil du være det koordinerende bindeled mellem de forskellige teams i QA, regulatorisk og Pharmacovigilance i relation til udfærdigelse eller opdatering af eksisterende TA.

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.

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.

Together with the rest of the team, you will be responsible for the daily support of our production lines. You will learn our processes in detail and gain a good overview of the documentation used in production.

Senior QA Specialist

The Senior QA Specialist for Radiometer is responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms. This is done by cooperating, supporting, facilitating, training, and communicating towards the best results with partners in R&D.

This position is part of the QA Design Control department, hybrid based and located in Brønshøj. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.

QA Specialist

You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms.

You will have the opportunity to:

• Provide Design Control guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment.
• Represent Quality Assurance in design and development projects and in cross-functional teams supporting new product development.

Continuous Improvement Partner

As a Continuous Improvement Partner in Drug Substance Manufacturing, you will be part of a team of Improvement Partners who develops and sustains systems and tools that enables the organization to consistently increase the level of operational excellence in manufacturing.

Your primary tasks will include but not be limited to:

• Develop and sustain CI systems and tools.
• Coach on ideal behaviour that drives a proactive improvement culture.

Senior Technical Writer - Regulatory (CMC)

You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.

Stepping into an informal and collaborative environment, you will have close interfaces with many different disciplines, including Global Pharmaceutical R&D, manufacturing sites, Product Supply, Quality Assurance, Ferring affiliates, and development sites around the world.

MS&T Program Manager

We are looking for an experienced professional from the pharmaceutical industry, who can effectively manage project plans across multiple entities and lead cross-functional processes within our own sites and supply chain.

As a MS&T Program Manager, you will be responsible for managing the projects, maintaining project databases, as well as ensuring effective communication and timely achievement of milestones.

Manufacturing Science & Technology (MS&T) Technical Transfer Project Manager (Sr Specialist)

Join Orifarm and take charge of building strong business relationships with a key portfolio of our suppliers!

As a MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to Supplier Relationship Management functions, and manufacturing sites comprising support, technological transfers between CMOs and own manufacturing sites, analytical method development and validation, external product development at CDMOs and driving continuous technological improvement and innovation.

Clinical Site Manager

Are you looking to make a significant impact on ensuring oversight of our outsourced clinical studies in Ferring Pharmaceuticals? Do you thrive in a global role that requires cross-functional collaboration?

In this role you will solidify the implementation of the Clinical Site Manager role. This role was recently introduced as being responsible for providing sponsor oversight of clinical site monitoring (outsourced to a CRO) and establishing strong relationships with clinical sites to ensure delivery of high-quality and timely clinical trials.

In this role you will be working closely with counterparts in the US and stakeholders at our International PharmaScience Center (IPC) in Copenhagen.

Clinical Evidence Lead

Do you want to:

• Lead the clinical development and clinical data strategy across application areas
• Lead the wording, substantiation, and documentation of clinical claims for regulatory compliance and commercial utilization
• Contribute to the clinical evidence activities in development projects and give input to PMCF

The main responsibilities of your new team are to drive the clinical strategies to ensure timely execution on clinical deliverables to support regulatory submissions and commercial strategies.