13 jobannoncer matcher din søgning 13 jobannoncer fundet

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.

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.

HSE Specialist

As an HSE Specialist, you will have the opportunity to develop and implement safety policies and procedures, conduct training sessions, and ensure compliance with local, state, and federal regulations.

In joining our team, you'll have the opportunity to make a significant impact, ensuring the safety and well-being of our workforce while contributing to our continued success at Duferco Danish Steel.

Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.

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 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.

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.

Protein Chemist for production of antibodies for cancer diagnostics

Do you find antibody production exciting?

You will play a key role in daily support of the production of conjugates. This can include:

• Support lab techs in case of technical issues with purification, conjugation, and test of antibodies.
• Handle compliance issues according to GMP standards.

We offer a high degree of freedom and development opportunities in an international company.

QA Team Manager

Er du passioneret omkring ledelse og udvikling, og kan du overføre glæden til et team af dedikerede specialister? Har du derudover erfaring indenfor QA og GMP, så har vi en interessant mulighed i vores Life cycle management og release afdeling.

I rollen som Team Manager bliver det din opgave at supportere et inkluderende miljø og fordre effektivt samarbejde i teamet af dygtige QA-medarbejdere. Derfor er det vigtigt, at du evner at specificere opgaver klart og tydeligt, definere mål og prioriteter, samt at du kan kommunikere og uddelegere ansvar i dit team.