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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.

Kvalitetskoordinator

I denne stilling får du mulighed for at udfordre dig selv i en dynamisk virksomhed, hvor der er højt til loftet og rig plads til udfoldelse. Du vil have tæt samarbejde med flere afdelinger i organisationen og mulighed for at præge kvalitetsområdet i betydelig grad.

Arbejdsopgaver vil bl.a. omfatte:

• Råvarekontrol, fra leverandørgodkendelse til implementering i produktionen samt leverandørreklamationer
• Udtagelse af prøver til ekstern analyse i henhold til fødevarelovgivning

Laborant

Har du øje for detaljen og fokus på kvalitet? Henter du samtidig energi via samarbejde, og kunne du tænke dig at blive vores 6. medlem i vores kvalitetslaboratorium?

Opgaverne omfatter blandt andet:

• Analyser og kontroller jf. vores kvalitetskontrolplan
• Support og samarbejde med produktionen
• Dokumentation og sikring af sporbarhed

Senior Technical Service Engineer, Global Hydrocracking

This is an opportunity to join a team, where we support the sale of catalysts and technologies that can help our customers world-wide in producing environmentally friendly fuels.

You will be involved in the technical part of the catalyst sales process preparing technical proposals and performance evaluations for our customers’ hydrocracking units. You will participate in internal projects to improve our calculation tools and knowledge creation within the field of upgrading heavy fossil and renewable hydrocarbons into valuable products.

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.

Aqua feed process technology - Innovation Scientist/Engineer

Do you have an interest in innovative process technology projects where you are part of developing the next generation of fish feed, looking into functional feed/food ingredients and technologies?

The position will focus on development of new feed types and applications, ingredient science and process technology knowledge.

You will join a great company with engaged colleagues and strong focus on innovation, furthermore health insurance, lunch arrangement at site, salary and other employee benefits which matches the market.

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.

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.

Clinical Supply Manager

The Clinical Supply Manager will be managing outsourcing of packaging, labelling, and distribution of clinical trial supplies for all clinical trials.

You must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.

We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.