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Laboratory Technician, Colour Anodizing

Are you driven by the challenge of mastering the art and science behind colour anodizing processes to shape the visual appeal and functionality across our wide product range?

Key responsibilities

• Identify and evaluate new technologies, tools, and methods within aluminium production.
• Lead and support implementation of special aluminium colour series.

With approximately 1100 employees, Bang & Olufsen is an agile company that gives room for individual flexibility and decision-making.

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

Senior Specialist til QC hos Xellia Pharmaceuticals

Drømmer du om mere ansvar, med forskelligartede opgaver, og har du en passion for mikrobiologi? Vil du spille en central rolle i Xellias produktionen af livsvigtig antibiotika?

Som senior specialist vil du blive faglig ansvarlig for vores count release-laboratorie, som bl.a. udfører TVC- og LAL-analyser. Derudover vil du indgå i tæt samarbejde med vores sterile produktioner angående EM, hvor de nye Annex 1-krav stiller øgede krav til vores compliance, som du vil spille en vigtig rolle i.

Sales Trader

We are looking for a Sales Trader who will play a vital role in ensuring BioCirc’s ambitious growth plans.

The successful candidate will together with the Portfolio Manager be responsible for the short-term sale of Certificates, optimizing the portfolio, gather market intelligence, and ensuring value added through the whole supply chain of biomethane production, but also new renewable products stemming from our energy clusters.

Team Lead, Technical Documentation & Support

Brænder du for teknisk dokumentation, og udvikling af intelligente akustikløsninger? Kan du omsætte teknisk viden til praksis og sikre høj kvalitet gennem detaljeret dokumentation? Vil du være en del af et internationalt orienteret firma, med solid erfaring inden for akustik, hvor bæredygtighed er et kernepunkt?

Med udgangspunkt i fremragende bygningsakustik søges en Team Lead til Technical Documentation & Support, der er et team, der varetager en række opgaver indenfor dokumentation, test & certificeringer og compliance.

Care for Potential – Trainee Program – Denmark

We believe that together we can create a sustainable tomorrow by caring for our resources. The Care for Potential Trainee Program, starting September 2nd, 2024, is a unique opportunity to use your potential and build your career while contributing to something of real value.

The purpose of the program is to provide ambitious young professionals with a structured framework and on-the-job training, as well as hands-on education and invaluable experiences. The program is designed to be both a digital and on-the-job experience with occasional travels, both nationally and internationally.

Department Manager for Molecular Pharmacology

Gubra is seeking a dedicated and experienced Department Manager to lead our Molecular Pharmacology department. The ideal candidate will possess proven leadership abilities and a passion for managing and developing teams, along with a background in molecular pharmacology and drug discovery.

Your tasks include

• Daily management of a team of scientists and lab technicians to ensure high performance, personal development, well-being and engagement.
• Guide the team to accomplish department goals and objectives.
• Oversee the planning, execution, and analysis of experiments to support Gubra’s internal and partnered drug discovery projects.

EHS Team Lead

The HSE Team Lead will report directly to the Head of HSE and will serve as the direct supervisor for a team of 8 skilled HSE professionals, comprising 4 HSE Officers and 4 Workflow Managers. This team is characterized by its dedicated members who excel in collaboration, mutual support, and fostering strong relationships with production teams.

As the Team Lead you will ensure that the team delivers high-quality work aimed at enhancing the factory's safety culture and preventing accidents.

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.

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 Environmental Impact Specialist

Are you passionate about making a difference in the apparel and textiles industry by measuring and communicating environmental impacts?

As a Senior Environmental Impact Specialist you act as the internal go-to specialist and it is expected that you engage with various stakeholders internally and externally to provide specialised knowledge.

Manager, Chemical Substance Registration

The Manager, Chemical Substance Registration is accountable for implementing and executing the chemical control compliance programs of IFF in the EAME region (UK, EU REACH, Turkey REACH, EAEU etc.) for the technical enzymes’ portfolio of products (Biofuels, Fabric & Household Care, Textile Processing and Designed Enzymatic Polysaccharides).

The Manager, Chemical Substance Registration is furthermore a key contact for the Enzyme Business in determining strategic business decisions and should be representing IFF in industry work groups to assure IFF’s regulatory interests.

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.