39 English-speaking jobs in Hillerød

Experienced Downstream Scientist needed for 12-month maternity cover. Lead and support technology transfers, develop project plans, and analyze manufacturing data to improve process performance.

Senior Global Product Manager will own and develop SSI Diagnostica Group's global Respiratory Diagnostics portfolio. Responsibilities include defining strategy, roadmap, and driving new product development and lifecycle management.

Experienced Downstream Scientist needed for 12-month maternity cover. Lead and support technology transfers, develop project plans, and analyze manufacturing data to improve process performance.

Driver/Data Collector needed for a 3-6 month project collecting images of streets, points of interest, and public areas in EU countries using 360 cameras. Must have a valid driver's license, good driving record, and be available for a minimum of 3 months.

Student assistant to support engineering team with tasks such as reviewing work orders, onboarding equipment, and preparing equipment for shipment. Must have a bachelor's degree or be finishing one in a relevant field and be proficient in Microsoft Office.

This is a combined clinical consultancy and clinical professorship position in Clinical Biochemistry at Copenhagen University Hospital - Rigshospitalet and the Faculty of Health and Medical Sciences, University of Copenhagen. The successful applicant will head the section involved in interpreting genomic data and be in charge of the bioinformatics section. Applicants must be board-certified specialists in Clinical Biochemistry.

Process Excellence Specialist will build and maintain global process governance, standards, and KPIs. Responsibilities include training process owners, developing process frameworks, and facilitating governance forums. Requires experience with process ownership, documentation, and cross-functional alignment.

Manage and maintain GxP and non-GxP IT systems, ensuring compliance with cGMP, GAMP, 21CFR Part 11, and internal quality standards. Serve as a single point of contact for system users, identifying and implementing new requirements, and leading small upgrade projects. Represent IT systems during audits and inspections, handling documentation and IT requirements for GxP critical systems. Develop and negotiate vendor service level agreements.

CSA Engineer needed for a pharmaceutical construction project. Supervise and support the installation of cleanroom finishes, conduct inspections, and collaborate with project teams. 2-3 years of experience in CSA pharma construction required.

Leads the Facility & Security function within Engineering & Operations Support, setting strategic direction and executing the site-wide facility and security strategy. Oversees facility maintenance, capital projects, and manages the department's operating budget.

Manage and maintain 10-15 IT systems essential to device design documentation and quality operations in a GxP environment. Ensure compliance with cGMP, GAMP, 21CFR Part 11, and internal quality standards.

Leads scientific direction for internal and external communications, bridging innovation with business strategy. Manages a team of scientific professionals and collaborates cross-functionally to support research, regulatory, medical affairs, product development, and commercial teams.

Process Safety Engineer to lead risk assessments, facilitate safety workshops, and ensure safe system start-up and handover.

Clinical consultant position in Endocrinology at Copenhagen University Hospital – Steno Diabetes Center Copenhagen combined with a 5-year clinical professorship in endocrinology with a focus on diabetes precision medicine and data-driven clinical quality at the University of Copenhagen. Applicants must be board-certified specialists in Internal medicine: Endocrinology and have documented clinical experience in treating diabetes.

The Product Owner will develop and manage products, ensuring they meet client needs and align with company strategy. Responsibilities include performing product CQAs, leading process gap assessments, and owning product risk assessments. The ideal candidate has a minimum of 5 years of product management experience, preferably in pharmaceuticals, and strong project management and communication skills.

Develops primary packaging systems and components for parenteral administration while coordinating and leading cross-functional projects. Responsibilities include planning and executing projects, managing resources and budgets, and collaborating with stakeholders and suppliers. Requires a M.Sc. or B.Sc. in Engineering, Pharmacy, or related field with at least 3 years of relevant experience.

Ensures products and services meet quality standards. Leads/supports customer audits and regulatory inspections, including logistics, evidence management, and CAPA plans. Collaborates with stakeholders to strengthen compliance processes and implement improvements. Maintains and improves the Pharmaceutical Quality System (PQS) aligned to ICH Q10 and ICH Q9.

QA Operations / QA Compliance Specialist to support quality activities in a GMP-regulated biopharmaceutical manufacturing environment. Will manage deviations, lead CAPA processes, conduct investigations, and review quality documentation. Requires experience with GMP regulations and quality systems.

Efor Group seeks a Tech Transfer Lead to manage technology transfer projects from development to commercialization. The role requires a Bachelor's or Master's degree in a relevant field and 5+ years of experience in technology transfer, process development, or manufacturing.

Product Owner to develop and manage products, ensuring they meet client needs and align with company strategy. Requires 5+ years of product management experience, preferably in pharmaceuticals. Strong communication, project management, and analytical skills are essential.