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Orifarm

Specialist, Regulatory Affairs (Temporary Position)

Odense S and Søborg

As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.

Further, your main responsibilities include to:

  • Gather information and documentation for variation applications
  • Update dossier sections
Orifarm
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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
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.

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Ferrosan Medical Devices A/S

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.

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.

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Senior MES Analysts for global system deployment

Bagsværd

Imagine your playground is the Manufacturing Execution System (MES) in large-scale production?

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Director of QC Module

Kgs. Lyngby

Are you an experienced leader with a strong background in project management?

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GMP Supporter

Hillerød

Do you enjoy challenges and working with several tasks at a time?

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Senior QA Profesional

Måløv

Are you passionate about setting direction within emerging technologies and ensuring compliance?

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(Senior) Strategy Project Manager

Bagsværd

Do you want to impact the strategic direction of Novo Nordisk Research & Early Development (R&ED) and drive projects to enable cutting-edge science and breakthrough innovation?

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Drug Product Senior Project Manager

Måløv

Are you passionate about driving drug product life cycle management projects for the benefit of our patients?

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Product Specialist - Oral Solid Dosage Forms

Måløv

Are you passionate about providing expert product knowledge and setting the direction for future tablet production to the benefit of our patients?

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Process Specialist

Måløv

Are you passionate about setting the technical direction for future tablet production to the benefit of our patients?

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Automation Validation Engineer

Måløv

Do you have experience with design, construction, and validation of automated equipment in pharma, and are you ready focus on quality and...

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