cqv

Vil du være med til at udvikle og lede Aconsils CQV-område?Aconsil er et projektkonsulenthus, der hjælper nogle af Danmarks førende pharma- og biotekvirksomheder. Vi søger en Head of CQV, som kan videreudvikle vores nuværende team og bidrage til den fortsatte vækst.Du bliver ansvarlig for et CQV-team med dygtige og engagerede konsulenter. Rollen...

Contract Opportunity | Onsite | Immediate StartWe’re supporting a leading biopharmaceutical manufacturing organisation seeking an experienced CQV Consultant to lead the development of a Master Validation Plan for a Drug Product programme.This is a hands-on contract position focused on establishing the first version of the Master Validation Plan while...

Job-Link A/S Senior CQV engineer with experience in Automation & IT Please note To be considered for this position, candidates must hold a valid work and residence permit for Denmark. Job-Link are seeking a highly skilled Automation & IT Specialist /Sr. Engineer to manage and execute various technical aspects of our customers projects in the pharma industry....

CQV Permit Office Manager – Post-ConstructionOverall PurposeThe CQV Permit Office Manager is responsible for controlling permit-to-work, LOTO, and safety governance during the CQV / commissioning phase of large and complex construction projects.The role ensures that commissioning is treated as a structured, high-risk execution phase, where activities are...

A leading process engineering firm in Gladsaxe Kommune is seeking process engineers to contribute to biopharmaceutical projects. Candidates should possess broad process knowledge and experience in GMP manufacturing. You will support project execution, ensuring technical solutions are optimized through collaboration with clients. This role offers a supportive...

A leading engineering firm in Denmark seeks a Senior CQV Engineer specializing in Automation & IT for pharma projects. You will manage project execution, develop documentation, and ensure compliance with regulatory standards. Ideal candidates should hold a Bachelor's in Electronics or Communication Engineering and possess over 12 years of automation...

A Knightec Group AB está formando uma equipe especializada para atuar em um projeto de grande porte na indústria farmacêutica, com foco em CQV de equipamentos e processos produtivos. A posição envolve colaboração com Engenharia, Produção e Qualidade para instalação, comissionamento, qualificação, validação e start-up.Buscamos profissionais com...

A leading process engineering firm in Gladsaxe Kommune is seeking process engineers to contribute to biopharmaceutical projects. Candidates should possess broad process knowledge and experience in GMP manufacturing. You will support project execution, ensuring technical solutions are optimized through collaboration with clients. This role offers a supportive...

Planet Pharma is seeking a Risk Coordinator for a pharmaceutical CQV project on-site in Hillerød/Hillerod area. You will coordinate RAMS activities across multiple workstreams, review method statements, and collaborate with PTW and LOTO coordinators to ensure safe commissioning and qualification activities.The role requires Pharmaceutical CQV experience,...

Head of CQV Vil du være med til at udvikle og lede Aconsils CQV-område? Aconsil er et projektkonsulenthus, der hjælper nogle af Danmarks førende pharma- og biotekvirksomheder. Vi søger en Head of CQV, som kan videreudvikle vores nuværende team og bidrage til den fortsatte vækst. Du bliver ansvarlig for et CQV-team med dygtige og engagerede...

Novo Nordisk A/S in Kalundborg, Denmark, is seeking a Senior Project Manager for Utilities in Recovery III to deliver critical utility systems on time and within scope. You will drive cross-functional collaboration and ensure successful delivery across interconnected work packages. You will work closely with engineering, maintenance and project teams,...

Risk Coordinator — Pharmaceutical CQV Project On-Site in Hillerod The Role As Risk Coordinator, you'll act as the daily coordinator and task manager for Risk Assessments and Method Statements (RAMS) across a large-scale Commissioning, Qualification and Validation (CQV) project. You'll be a visible, hands‑on presence on site — facilitating risk...

Planet Pharma is seeking a Risk Coordinator for a pharmaceutical CQV project on-site in Hillerød/Hillerod area. You will coordinate RAMS activities across multiple workstreams, review method statements, and collaborate with PTW and LOTO coordinators to ensure safe commissioning and qualification activities. The role requires Pharmaceutical CQV experience,...

At alba, we work with process engineering across the full project lifecycle – in close collaboration with our customers – from concept and design to start‑up, CQV, and onwards to stable production. Working at alba Our team’s strength lies in operational experience. We know how a production facility actually runs, and we use that insight to support...

At alba, we work with process engineering across the full project lifecycle – in close collaboration with our customers – from concept and design to start‑up, CQV, and onwards to stable production. Working at alba Our team’s strength lies in operational experience. We know how a production facility actually runs, and we use that insight to support...

FUJIFILM Biotechnologies (FLBD) is seeking an experienced Validation Engineer / Validation Subject Matter Expert (SME) to drive validation activities related to Controlled Temperature Units (CTUs) including Refrigerator, Freezer, Cold room, Warehouse and Incubator. This is a highly visible role requiring deep technical expertise, strong regulatory knowledge,...

FUJIFILM Biotechnologies (FLBD) is seeking an experienced Validation Engineer / Validation Subject Matter Expert (SME) to drive validation activities related to Controlled Temperature Units (CTUs) including Refrigerator, Freezer, Cold room, Warehouse and Incubator. This is a highly visible role requiring deep technical expertise, strong regulatory...

FUJIFILM Biotechnologies (FLBD) is seeking an experienced Validation Engineer / Validation Subject Matter Expert (SME) to drive validation activities related to Controlled Temperature Units (CTUs) including Refrigerator, Freezer, Cold room, Warehouse and Incubator. This is a highly visible role requiring deep technical expertise, strong regulatory...

Jobbeskrivelse Kalundborg, Denmark Jobkategori Project Management & Agile Are you ready to lead complex utility projects that play a vital role in large-scale pharmaceutical production? Join us as a Senior Project Manager in Recovery III and take ownership of critical utility deliveries. This is your opportunity to shape execution, drive collaboration, and...

Risk Coordinator — Pharmaceutical CQV Project On-Site in Hillerod The Role As Risk Coordinator, you'll act as the daily coordinator and task manager for Risk Assessments and Method Statements (RAMS) across a large-scale Commissioning, Qualification and Validation (CQV) project. You'll be a visible, hands‑on presence on site — facilitating risk...