Archived jobs

A stimulating job in our MSAT Process Validation Team, in Copenhagen as an experienced, experienced Process Validation Specialist (Principal Scientist) is open for a quality-minded new colleague with biopharmaceutical processing experience. The Job AGC Biologics continues to enjoy great success, with a steadily increasing number of projects – many of which are late stage development projects preparing for commercial launch, as well as launched projects. More specifically, we have several projects active in the process validation stages from initial process risk assessment to execution of PPQ ...

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Are you looking for an exciting job in a fast-growing international CDMO organization producing new biological medicines? Do you enjoy working in a dynamic environment, where you every day will be involved in multiple different tasks of varying complexity? QC Bioassay is looking for a Scientist (maternity cover, 12 months) to be part of our Scientist team. AGC Biologics A/S is a global CDMO, where we work with the development of biopharmaceutical manufacturing processes and GMP manufacturing of biopharmaceutical proteins for both clinical testing and marketing. We are working in an ...

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A challenging job is open for a quality-minded scientist within the Process Validation Department in Copenhagen, which requires process validation knowledge, ability to drive validation studies and manage internal and external stakeholders in different projects. The role of Process Validation Scientist offers opportunity to lead, coordinate and oversee process validation activities for late stage projects from initiation to completion. The Process Validation Scientist will be responsible for providing technical inputs and support to internal and external stakeholders in different projects, as ...

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With AGC Biologics increasing activities, we are looking for a new scientist with experience within Facility compliance in the pharmaceutical industry. AGC Biologics is a Contract Manufacturing Organization (CDMO) with facilities in Denmark, Germany, Japan and USA and with customers from all over the world. We have more than 50 nationalities employed and the daily language is English. The Facility Compliance team The Facility Compliance team is supporting all the manufacturing departments with tasks related to ensuring compliance with the facility. Facility compliance includes support related ...

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If you are a highly qualified and experienced QP, we invite you to apply for our opening at AGC Biologics. Join us in our mission to make a difference in the lives of patients worldwide. Job Description: As a QP (Delegate) at AGC Biologics you will play a pivotal role in ensuring the quality and compliance of our pharmaceutical operations. Your responsibilities will encompass the following key areas: Responsibilities: Batch Disposition: Take on the crucial responsibility of batch disposition to guarantee the quality and safety of our pharmaceutical products. GMP Subject Matter Expert (SME) ...

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Are you a network builder with a strong, holistic Quality mindset, and looking for a job where your contribution has a direct impact on our growing success? Then we have the perfect job for you. AGC Biologics is a leading global Contract Development and Manufacturing Organization, with a deep commitment to improving life quality by bringing new biopharmaceuticals to market. Because of our dedication to building and empowering our internal teams, AGC Biologics is an innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As such, we deliver a ...

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Would you like to be a part of AGC Biologic’s growing success? We are looking for a QA Principal Scientist with a passion for GMP facilities and equipment. AGC Biologics is a leading global Contract Development and Manufacturing Organization, with a deep commitment to improving life quality by bringing new biopharmaceuticals to market. Because of our dedication to building and empowering our internal teams, AGC Biologics is an innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As such, we deliver a deep expertise, dynamic solutions and ...

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Our team is growing, and we are looking for an experienced QA scientist to assist with Quality Assurance of Material Management QA for Material Management is an important part of the Quality organization. You will be joining a diverse team of highly qualified colleagues, all with several years of experience within quality assurance. This QA team is responsible for support of supply chain and QC in the areas for deviations, CAPA, change management, complaints, GMP documentation etc. in relation to material management. We also have oversight of the respective areas and assist with internal and ...

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AGC is looking for a Scientist with expertise with analysis of protein based biotherapeutics We are seeking a scientist with a strong scientific profile within analysis of proteins focused on HPLC and capillary electropresis techniques in in the Analytical Development (AD) Department at AGC Biologics A/S (AGC). AGC is a Contract Development and Manufacturing Organization with facilities in Denmark, Germany, Italy, Japan and USA and with customers all over the world. The department The AD Department is responsible for implementation, transfer and development of analytical procedures, analytical ...

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Are you looking for an exciting job in an international and challenging environment? Do you thrive in a dynamic environment, in a department with skilled colleagues in an organization where we work as one team? This is a great opportunity to make the most of your expertise and passion for analytical chemistry. At AGC Biologics A/S (AGC), we work with the development of biopharmaceutical manufacturing processes and GMP manufacturing of biopharmaceutical proteins for both clinical testing and marketing. Since we are a contract manufacturing organization, a high level of service to our clients is ...

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