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Specialist, Regulatory Affairs (Temporary Position)

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

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?

Miljømedarbejder til grundvandsgruppen

Brænder du for at give et bedre miljø videre til de næste generationer? Vil du være med til at arbejde for at fremme drikkevandskvaliteten og en grundvandsudnyttelse i balance i Tønder Kommune?

Du vil være myndighed på drikkevandsområdet, det vil sige træffe myndighedsafgørelser, give markvandingstilladelser, samarbejde med vores lokale vandværker om drikkevandskvaliteten og føre tilsyn med dem og meget mere.

Du får god mulighed for personlig og faglig udvikling i form af sidemandsoplæring, deltagelse i kurser og efteruddannelse.

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.

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.