Denmark Job Openings
AGC Biologics
Scientist, Manufacturing
Copenhagen
FULL TIME
September 9, 2024
Do you have experience working in a c GMP environment and are you looking for new opportunities for further growth? Then this position could be something for you.
RESPONSIBILITIES:
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Responsible for/Consulted during MPR creation on process steps to align production flow and GDoc P requirements
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Daily review of documentation in production
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Accountable for timely batch review according to KPI
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Accountable for timely deviation closure (incl. systematic problem-solving during root cause investigation) according to KPI
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Responsible for enabling timely batch release
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Responsible for data feedback/status on release process
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Responsible for capturing learnings and align with MPR template owner to continuously improve MPR template
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Responsible for sharing knowledge across project groups
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Experience in preferably in commercial/commercial GMP manufacturing.
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Have experience with and demonstrated understanding of Good Manufacturing Practices (GMP)
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Have experience writing, reviewing and approving GMP documentation.
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Experienced with operations of single-use technologies and aseptic processing.
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Self-motivated, organized and proactive.
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Ability to coordinate multi-departmental tasks and deliverables (interaction with Process Transfer, Process Development, Engineering, QA, QC, etc.).
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Experience working with multiple projects simultaneously.
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Demonstrated experience leading troubleshooting efforts.
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Strong communication skills necessary to interact with internal and external stakeholders.
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Strong presentation skills.
Want to keep posted about our growth and to learn more about our company?
AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical c GMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.
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Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (p DNA), messenger RNA (m RNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with c GMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on
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