Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market. GMP - Technical Training Specialist Would you like to be part of developing GMP training material and delivering effective technical onboarding programs, and do you have what it takes to play a pivotal role in our Manufacturing Training Department. If so, then read on as you could be our new GMP - Technical Training Specialist. Our products would not make it in the hands of the patients without our highly skilled manufacturing teams. As our new Technical Training Specialist, you will be at the heart of the organization, training and developing new and current Manufacturing employees. Training such as Aseptic Behaviour, Gowning Procedures and train the trainer programs using TWI methodology. What will you do? The Technical Training Specialists will play an active role in training and on-boarding our Manufacturing employees. To succeed in this role it is vital that you have previously worked within the biopharmaceutical industry, and you have your finger on the pulse of training and behavioral requirements within a GMP manufacturing environment. You have extensive experience within training/education and delivery of technical topics within biopharmaceutical manufacturing industry. Alongside other Technical Training Specialists, you will train our new hires throughout their on boarding journey, delivering theoretical and practical manufacturing training such as Aseptic Behavior, Gowning, Daily Sampling, whilst ensuring that they have adopted a quality and training mindset prior to entering our manufacturing facilities. You will need to work analytically with Managers, Team Leads and SMEs from various departments to identify and understand their business processes, assess training needs, opportunities and gaps, and implement effective solutions. You will also assist with administrative tasks in relation to training documentation, systems, compliance, reporting, writing technical training material and planning of training activities. What do you need to succeed in this role? You hold a relevant education/experience and have previously worked in a similar position as a technician/scientist for at least 3-5 years within GMP production of API/Drug Product manufacturing. Strong, detailed knowledge and understanding of GMP biopharmaceutical manufacturing processes. Skilled in the application of adult learning theories, training facilitation and delivery. You enjoy delivering dynamic classroom training. You have the ability to create and revise technical training materials to keep pace with best practice. You effectively present information and ideas formally and informally, verbally and in writing (in English). Experience with, or understanding of, TWI (Training Within Industry) and LEAN methodology. You know Office 365 features by heart and ideally you already have experience in developing eye catching and engaging e-learning content (e.g. using Articulate 360, video recording and editing etc.) and other creative training material/presentations. Experience with video creation and editing is desirable. On a personal level You're eager to be part of our vibrant team, adding to the enjoyable and collaborative atmosphere – a good sense of humor is essential! Thriving in a fast-paced, dynamic environment comes naturally to you, and you tackle challenges with a smile. Join forces with us to uphold our stellar reputation, working seamlessly as a unified team. Your proactive nature and pragmatic approach ensure that you maintain high-quality work, even in a fast-moving environment. While you're independent, you also value teamwork and service. You approach tasks with enthusiasm, curiosity, and positivity. With a focus on quality, you actively seek avenues for improvement and advocate for positive transformations. Your communication skills are top-notch, with a strong command of English. You identify with our core values - TRUST, INGENUITY, QUALITY, KNOWLEDGE, TEAMWORK & ACCOUNTABILITY 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 (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-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 LinkedIn and give us a quick Like on Facebook! AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. 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 (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-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.