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QA Ext. Manufacturing Specialist

Would 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.

Quality Assurance Specialist

Har du erfaring med kvalitetsarbejde, hvor beslutninger om leverancer og produktkvalitet også træffes ud fra vurderinger og praktiske hensyn?

Trioworld er en førende producent af emballageløsninger baseret på polyethylen- og polypropylenfilm.

Du kommer til at forandre og udvikle den systematiske og operationelle håndtering af interne afvigelser og eksterne reklamationer.

Manufacturing Supporter

We are looking for a talented Manufacturing Supporter for the Drug Substance Production to join the DS Documentation and Support Department in Hillerød.

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us.

You will be part of a team, consisting of 14 people, with a great sense of humor and a high willingness to support where needed.

Quality Assurance Specialist

Er du god til at gøre krav og regler meningsfulde og forståelige over for dine kollegaer? Så har vi en spændende stilling i vores QA-afdeling til dig.

Quality Assurance er en central og vigtig del af vores værdikæde. Einar Willumsen (EW) er certificeret efter BRC Standard for Food Safety, og din opgave bliver at medvirke til at sikre en fortsat høj standard med stort fokus på kvalitets- og fødevaresikkerhedskultur.

Vi tilbyder et spændende og udfordrende job i en kultur, hvor samarbejde vægtes højt. Du bliver en del af en international virksomhed med mange muligheder for personlig udvikling. Og en ting kan vi love: det bliver aldrig kedeligt.

Coop Trading is looking for a technical expert to handle cosmetics and personal care products

Do you have a technical background within chemistry or pharmacy, and are you curious by nature to learn more, e.g. about developing products for retail?

You will develop an attractive and competitive personal care and cosmetic product portfolio for the Nordic Private Brand market in close cooperation with the team and suppliers. You wil also quality assure that the portfolio complies with Coop's high standards within safety, sustainability, consumer information and quality.

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.

Technical Writer to GE HealthCare Denmark

Join GE HealthCare to help develop high quality instructions for use for our ultrasound scanners, transducers, and reprocessing methods in compliance with rules and legislation in various countries. 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.

Our Technical Documentation team consists of six dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities. Our Technical Writers develop and maintain the user documentation for our high-performance equipment.

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.